524 Epidemiology Jobs

Zeelab Pharmacy is looking for Pharmacist - Varanasi (Varanasi) to join our dynamic team and embark on a rewarding career journey Compounding and dispensing medications, as prescribed by physicians. Monitoring customers drug therapies, advising interventions, and informing customers of any potential side effects. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment. Completing operational requirements of the pharmacy, including verifying order entries, maintaining records of controlled substances, charges, and removing expired and/or damaged drugs from the pharmacys inventory. Adhering to applicable legal rules, regulations, and procedures governing pharmaceutical practice. Performing other administrative tasks when needed.

Zeelab Pharmacy is looking for Pharmacist- Lucknow (Lucknow) to join our dynamic team and embark on a rewarding career journey Compounding and dispensing medications, as prescribed by physicians. Monitoring customers drug therapies, advising interventions, and informing customers of any potential side effects. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment. Completing operational requirements of the pharmacy, including verifying order entries, maintaining records of controlled substances, charges, and removing expired and/or damaged drugs from the pharmacys inventory. Adhering to applicable legal rules, regulations, and procedures governing pharmaceutical practice. Performing other administrative tasks when needed.

Zeelab Pharmacy is looking for Pharmacist - Mumbai (Mumbai) to join our dynamic team and embark on a rewarding career journey Compounding and dispensing medications, as prescribed by physicians. Monitoring customers drug therapies, advising interventions, and informing customers of any potential side effects. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment. Completing operational requirements of the pharmacy, including verifying order entries, maintaining records of controlled substances, charges, and removing expired and/or damaged drugs from the pharmacys inventory. Adhering to applicable legal rules, regulations, and procedures governing pharmaceutical practice. Performing other administrative tasks when needed.

Job Description Position: Medical Coder Ct: HR HR Shanmugapriya - 8072891550 Medical Coding is the process of converting patient health information into alpha numeric codes. Coders take medial reports from doctors, which may include a patients condition, the doctors diagnosis, a prescription, and whatever procedures the doctor or healthcare provider performed on the patient, and turn that into a set of codes, which make up a crucial part of the medical claim. Eligibility All (UG/PG) Life Science Paramedical Graduates BDS BPT BHMS BAMS Siddha,Unani,Naturopathy {Dip Bsc Msc} Nursing/GNM {B.E M.E} Biomedical Engineering {B.tech,M.tech}Biotechnology Biochemistry Bioinformatics Microbiology Zoology and Advanced zoology Biology Botany Medical Lab Tech Plant biotechnology Pharmacy(B.Pharm M.pharm) Paramedical Physiotherapy Physician assistant Critical Care Technology Medical Biochemistry Medical Record Science Operation Theatre Anaesthesia Technology {Bsc Msc Dip} Clinical Nutrition Human Genetics Medical Laboratory Technology Medical Sociology Epidemiology Molecular Virology Biostatistics Blood Banking Technology Regenerative Medicine Optom. Genetic Counseling Radiology Imaging Technology Medical Biochemistry Medical Microbiology Clinical Care Technology Clinical Care Technology Medical Physics {Bsc Msc Dip} Accident Emergency Care Technology Audiology speech Language Pathology Cardiac Technology Cardio Pulmonary Perfusion Care Technology Critical Care Technology Dialysis Technology Neuro Electrophysiology Medical Sociology Nuclear Medicine Technology Operation Theatre Anaesthesia Technology Optometry Physician Assistant Radiology Imaging Technology Radiotherapy Technology Medical Record Science Respiratory Therapy Fitness and Lifestyle Modifications Accident Emergency Care Technology Critical Care Technology Nursing Aide Operation Theatre Anesthesia Technology Ophthalmic Nursing Assistant Medical Record Science Optometry Technology Radiology Imaging Technology Medical Lab Technology Cardiac Non Invasive Technology Dialysis Technology Dentist Requirement Knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills Benefits System based job Weekly 5 days duty Day shift with Sat and Sun off Food and Cab provided by company Incentives based on performance Starting salary 12k to 25k with increment in 6 months for experienced. Abroad opportunities available Bonus for referring friends Medical expenses covered by company Provident Fund will be provided Gratuity after 5 yrs of work experience. Job Location: Chennai, Coimbatore, Vellore, Trichy, Cuddalore, Pondi Salem, Erode, Namakkal, Thanjavur, Nagercoil, Theni,Dindokal Thiruvannamalai, Villupuram, Karur, Tirunelveli,Kanniyakumari Tirupati, Kerala, AP,Tamilnadu,Telangana Ct: HR HR Shanmugapriya - 8072891550 This job is provided by Shine.com

About The Job Our Team: Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main Responsibilities The Principal Biostatistician will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans (SAP), programming specifications for analysis datasets and provide QC done data packages including tables, figures, and listings for use in publications (i.e., abstracts, posters, oral, presentations, manuscripts and ad-hoc data analysis requests) and to investigate the natural history of a TA diseases and long-term treatment outcomes of observational data using clinical trials and / or Registries as applicable; The Principal Biostatistician will ensure SOPs are followed, communications, timelines and quality metrics are met.; Collaboration of Local biostatistics and programming teams, Global Medical Affairs biostatisticians and / or programmers, and Global Medical Affairs Scientific Communications personnel . People Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and programming team members within the allocated Global business unit and product – with an objective to develop statistical data outputs. Support Sanofi Business Operations Leadership Team in understanding of stakeholders needs & expectations and provide end to end solutions for TAs/indications. Coach/mentor new team members to support efficient and quick onboarding. Support graduate hiring program as needed. Performance / Process Conduct appropriate post-hoc or ad-hoc statistical analyses of clinical trial data and / or registry (i.e., Observational) data. Design, develop, test, implement, and document statistical programming in high-level software packages e.g. SAS. Produce well documented data packages that include tables, listings, and figures. Work closely with the Team Lead Biostatistician and/or Team Lead Programmer to develop and implement project QC plans, timelines and KPIs. Learn, implement, and share through lecture series at least one indication of disease and product (Immunology, Multiple Sclerosis and Neurology, Rare Diseases, Rare Blood Disorders and Oncology) expertise. Review appropriate biomedical and clinical research literature related to assigned project(s). Active participation and Effective contributing in project governance meeting to proactively discuss risks, issues related to timelines and quality of deliverables. Present your selected / assigned topic in lecture series internal and / or across line functions thereby improving the statistical knowledge and presentation skills. Use Advanced analytical methods & tools to provide dashboards to the stakeholders. Customer Work closely with Global Medical Affairs biostatisticians and/or programmers to identify statistical analysis needs and assist in developing assigned deliverables About You Experience : Master's degree 8 years (M.Sc.) of experience required /Ph.D. in biostatistics or statistics or epidemiology (preferred) and 4 years. Soft skills : Stakeholder management, Ability to manage timelines and Ability to work independently and within a team environment, High proficiency in statistical methods used in the pharmaceutical industry, Autonomy in the management of activities; ability to manage multiple conflicting high priority deadlines. Technical skills : Advance SAS programming skills, SDTM & ADaM (CDISC) and other statistical computing software skills in a clinical data environment across multiple therapeutic areas. Education : Master of Science degree or equivalent in Statistics/ Ph.D. in biostatistics or statistics or epidemiology Languages : Excellent English language knowledge – written and spoken Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! null Pursue Progress . Discover Extraordinary . Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together. At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

About the job Our Team: Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main responsibilities: The Principal Biostatistician will work with Medical Affairs biostatisticians and/or programmers and Sanofi Business Operations biostatistics and programming personnel to implement statistical analysis plans (SAP), programming specifications for analysis datasets and provide QC done data packages including tables, figures, and listings for use in publications (i.e., abstracts, posters, oral, presentations, manuscripts and ad-hoc data analysis requests) and to investigate the natural history of a TA diseases and long-term treatment outcomes of observational data using clinical trials and / or Registries as applicable; The Principal Biostatistician will ensure SOPs are followed, communications, timelines and quality metrics are met.; Collaboration of Local biostatistics and programming teams, Global Medical Affairs biostatisticians and / or programmers, and Global Medical Affairs Scientific Communications personnel . People: 1) Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and programming team members within the allocated Global business unit and product – with an objective to develop statistical data outputs. 2) Support Sanofi Business Operations Leadership Team in understanding of stakeholders needs & expectations and provide end to end solutions for TAs/indications. 3) Coach/mentor new team members to support efficient and quick onboarding. 4) Support graduate hiring program as needed. Performance / Process: 1) Conduct appropriate post-hoc or ad-hoc statistical analyses of clinical trial data and / or registry (i.e., Observational) data. 2) Design, develop, test, implement, and document statistical programming in high-level software packages e.g. SAS. 3) Produce well documented data packages that include tables, listings, and figures. 4) Work closely with the Team Lead Biostatistician and/or Team Lead Programmer to develop and implement project QC plans, timelines and KPIs. 5) Learn, implement, and share through lecture series at least one indication of disease and product (Immunology, Multiple Sclerosis and Neurology, Rare Diseases, Rare Blood Disorders and Oncology) expertise. 6) Review appropriate biomedical and clinical research literature related to assigned project(s). 7) Active participation and Effective contributing in project governance meeting to proactively discuss risks, issues related to timelines and quality of deliverables. 8) Present your selected / assigned topic in lecture series internal and / or across line functions thereby improving the statistical knowledge and presentation skills. 9) Use Advanced analytical methods & tools to provide dashboards to the stakeholders. Customer: Work closely with Global Medical Affairs biostatisticians and/or programmers to identify statistical analysis needs and assist in developing assigned deliverables About you Experience : Master's degree 8 years (M.Sc.) of experience required /Ph.D. in biostatistics or statistics or epidemiology (preferred) and 4 years. Soft skills : Stakeholder management, Ability to manage timelines and Ability to work independently and within a team environment, High proficiency in statistical methods used in the pharmaceutical industry, Autonomy in the management of activities; ability to manage multiple conflicting high priority deadlines. Technical skills : Advance SAS programming skills, SDTM & ADaM (CDISC) and other statistical computing software skills in a clinical data environment across multiple therapeutic areas. Education : Master of Science degree or equivalent in Statistics/ Ph.D. in biostatistics or statistics or epidemiology Languages : Excellent English language knowledge – written and spoken Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! null

Job Title: Area Medical Advisor, Vaccines Position Summary: This role offers an exciting opportunity to make a meaningful impact on public health. You will provide scientific and medical expertise to support healthcare professionals and ensure accurate medical information is shared. Collaboration is key—you’ll work closely with cross-functional teams and external experts to drive scientific engagement. We value candidates who are proactive, detail-oriented, and passionate about improving health outcomes. Responsibilities: Build and maintain strong relationships with healthcare professionals and external experts. Deliver scientific presentations at medical education events, workshops, and conferences. Support the development and execution of medical strategies aligned with business goals. Stay updated on the latest scientific research and ensure accurate, compliant communication. Provide medical input for research feasibility assessments and field studies. Contribute to pharmacovigilance activities to ensure patient safety. Qualifications/Skills: Basic: MBBS or equivalent medical degree. Strong communication skills in English and local language. Experience presenting scientific topics in professional settings. Understanding of scientific methods and experimental design. 2–5 years of experience in the pharmaceutical, vaccines, or biologicals industry. Preferred: Postgraduate qualification in Public Health, Pharmacology, or related fields. Research experience in immunology, epidemiology, or infectious diseases. Familiarity with ICH-GCP principles and industry codes. Proven ability to build relationships with healthcare professionals and key opinion leaders. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. It has come to our attention that the names of GlaxoSmithKline or GSK or our group companies are being used in connection with bogus job advertisements or through unsolicited emails asking candidates to make some payments for recruitment opportunities and interview. Please be advised that such advertisements and emails are not connected with the GlaxoSmithKline group in any way. GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable. If you come across unsolicited email from email addresses not ending in gsk.com or job advertisements which state that you should contact an email address that does not end in “gsk.com”, you should disregard the same and inform us by emailing askus@gsk.com, so that we can confirm to you if the job is genuine.

Responsibilities May supervise Biostatisticians, Associate Biostatisticians and SAS programmers (all levels) and direct their work on clinical research studies. Provides expert consultation to projects across the company on statistical methodology. Solves problems of complex statistical scope. Provides technical review of proposed statistical design for research studies across company. Serves as the lead Biostatistician on one or more study projects. Participates in statistical process development and improvement across company. May present at statistical conferences. Provides sound strategic, scientific and statistical input to support client’s research projects. Leads the project team’s development of study analysis plans and statistical programs to perform analyses and display study data. Keeps abreast with current statistical and medical literature to ensure that sound methodologies are adopted. Fosters innovation in Biostatistics that will continuously enhance current statistical knowledge and practices. Ensures the scientific integrity of the research project and the accuracy of the reported results. Performs sample size calculation and provides leadership in the statistical design of research projects. Reviews protocols and case report forms to ensure that protocol objectives are met, and standards are maintained. Develops study assignment allocation schemas along with appropriate documentation. Leads the development of the methods and results sections of clinical study reports and scientific publications. Represents Client on behalf of clients at regulatory meetings. Provides expertise in methodological advances both internally and externally to improve statistical methodologies. Participate in the development and updating of Standard Operating Procedures. Other duties as assigned Qualifications MS in biostatistics, statistics, or PhD in biostatistics, statistics, epidemiology or related field At least 4 years of related experience with MS or 1 year of related experience with PhD is expected but not required. Experience with methodological statistical research, including publication and/or presentation of work in statistical methods development. Demonstrated proficiency with statistical methods and applications in clinical research. Strong programming skills in SAS and/or R. Expertise in state-of-the-art data manipulation and statistical methodology. Excellent communication, interpersonal and organization skills. Ability to manage multiple tasks. Ability to work independently, as well as in a team environment. Ability to effectively communicate complex statistical concepts, both written and oral.

Medcare Hospitals Medical Centres is looking for Pharmacist to join our dynamic team and embark on a rewarding career journey Compounding and dispensing medications, as prescribed by physicians. Monitoring customers drug therapies, advising interventions, and informing customers of any potential side effects. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment. Completing operational requirements of the pharmacy, including verifying order entries, maintaining records of controlled substances, charges, and removing expired and/or damaged drugs from the pharmacys inventory. Adhering to applicable legal rules, regulations, and procedures governing pharmaceutical practice. Performing other administrative tasks when needed. Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before

Role & responsibilities An Assistant Professor in Community Medicine is a faculty position focused on public health, epidemiology, and preventive medicine within a medical or public health context . They are responsible for teaching, conducting research, and contributing to community health initiatives, often working with various stakeholders to improve community well-being. Teaching: Delivering lectures, seminars, and practical sessions to undergraduate and postgraduate students in areas like epidemiology, disease prevention, and health promotion. Research: Conducting research projects related to community health, developing research proposals, and publishing findings in peer-reviewed journals. Community Health Initiatives: Participating in community health programs, collaborating with public health experts and government agencies to address health challenges, and developing and implementing public health initiatives. Clinical Involvement: Providing preventive and promotive care in community settings, contributing to the development of health policies, and offering expertise in relevant areas. Mentorship: Mentoring and supervising students in their research projects and academic pursuits. Interdisciplinary Collaboration: Working with other faculty members, health professionals, and community stakeholders to improve community health outcomes. Required Qualifications and Experience: Doctorate (PhD) or equivalent: A PhD in public health, epidemiology, or a related field is generally required. Postgraduate Medical Degree: While not always mandatory, a postgraduate medical degree (e.g., MD in Community Medicine) is often preferred for positions involving clinical practice. Research Experience: Demonstrated research experience, publications, and grant-seeking skills are highly valued. Teaching Experience: Prior teaching experience, preferably in a university or academic setting, is an asset. Strong Communication Skills: Excellent communication, interpersonal, and presentation skills are essential for teaching, research, and community engagement. MD's , MBBS, Ph.D in community Medicine qualification Preferred candidate profile

Job Description Key role requirements for this position: Subject Expertise: Apply in-depth knowledge of public health, epidemiology, and preventive medicine to address community health challenges. Teaching & Curriculum: Design and deliver updated, engaging content for medical and public health students, including practical field training. Research Contributions: Lead research in public health areas, publish in reputed journals, and secure funding for impactful community projects. Mentorship: Guide students and junior faculty in academics, research, and career development in community-based healthcare. Community Collaboration: Partner with public health bodies and NGOs to drive health initiatives and participate in outreach programs. Clinical Involvement: Offer preventive and promotive care in community or primary healthcare settings, linking theory to practice. Administrative Roles: Contribute to academic governance through committee work, policy input, and support for institutional goals. Continuous Learning: Engage in ongoing professional development to stay updated with evolving trends and policies in community health. Academic Qualifications MBBS+MD(Community Medicine) Full time 1700k Year Community Medicine Community Medicine Full time 1700k Year

Life-changing careers - Check out this open position at Novo Nordisk Senior Global HEOR Manager Job description Job description Are you passionate about driving market access preparedness and demonstrating the value of healthcare products Do you have experience in Health Economics and Outcomes Research We are looking for a Sr. Global HEOR Manager to join our team in Novo Nordisk. If you are ready for a challenging and impactful role, read on and apply today for a life-changing career. As a Sr. Global HEOR Manager at Novo Nordisk, you will be responsible for:Supporting the Health Economics and Outcomes Research strategies and plans to contribute to market access preparedness for pipeline and launch products and to demonstrate the Health Economics and Outcomes Research value of the Novo Nordisk Diabetes products. Provide strategic inputs in market access decision making, address the fundamental payer needs and build economic value arguments to secure reimbursement and broader market access of Novo Nordisk products. Support in driving HEOR strategy for NN Diabetes pipeline products in collaboration with DK team.Support the Diabetes access team in driving team s growth.Demonstrates subject matter knowledge and professional application.Demonstrates project management capabilities in driving projects. Qualifications To be our new Sr. Global HEOR Manager, we are looking for a candidate with the following qualifications: University master s degree in appropriate field such as health economics or outcomes research, epidemiology or statistics/biostatistics. Documented training in health economics or outcomes research.More than six years of experience in health economics and health outcomes research, ideally within pharmaceutical industry or consultancy. Scientific publication track record (in peer-reviewed manuscripts) is preferable.Effective communication skills. Stakeholder management (both within BLR & DK)The Commercial, Global Business Services (GBS) unit is responsible for driving deliverables for multiple Corporate Vice President (CVP) areas within Commercial, GBS, including Insulin, GLP-1 and Obesity Marketing, Market Access, Commercial Planning and Commercial Operations. The Commercial, GBS unit also supports BioPharma global marketing for Hemophilia and growth disorders. Working at Novo Nordisk

Life-changing careers - Check out this open position at Novo Nordisk Senior Global HEOR Manager Job description Job description Are you passionate about driving market access preparedness and demonstrating the value of healthcare products Do you have experience in Health Economics and Outcomes Research We are looking for a Sr. Global HEOR Manager to join our team in Novo Nordisk. If you are ready for a challenging and impactful role, read on and apply today for a life-changing career. As a Sr. Global HEOR Manager at Novo Nordisk, you will be responsible for:Supporting the Health Economics and Outcomes Research strategies and plans to contribute to market access preparedness for pipeline and launch products and to demonstrate the Health Economics and Outcomes Research value of the Novo Nordisk Diabetes products. Provide strategic inputs in market access decision making, address the fundamental payer needs and build economic value arguments to secure reimbursement and broader market access of Novo Nordisk products. Support in driving HEOR strategy for NN Diabetes pipeline products in collaboration with DK team.Support the Diabetes access team in driving team s growth.Demonstrates subject matter knowledge and professional application.Demonstrates project management capabilities in driving projects. Qualifications To be our new Sr. Global HEOR Manager, we are looking for a candidate with the following qualifications: University master s degree in appropriate field such as health economics or outcomes research, epidemiology or statistics/biostatistics. Documented training in health economics or outcomes research.More than six years of experience in health economics and health outcomes research, ideally within pharmaceutical industry or consultancy. Scientific publication track record (in peer-reviewed manuscripts) is preferable.Effective communication skills. Stakeholder management (both within BLR & DK)The Commercial, Global Business Services (GBS) unit is responsible for driving deliverables for multiple Corporate Vice President (CVP) areas within Commercial, GBS, including Insulin, GLP-1 and Obesity Marketing, Market Access, Commercial Planning and Commercial Operations. The Commercial, GBS unit also supports BioPharma global marketing for Hemophilia and growth disorders. Working at Novo Nordisk

Life-changing careers - Check out this open position at Novo Nordisk Senior Global HEOR Manager Job description Job description Are you passionate about driving market access preparedness and demonstrating the value of healthcare products Do you have experience in Health Economics and Outcomes Research We are looking for a Sr. Global HEOR Manager to join our team in Novo Nordisk. If you are ready for a challenging and impactful role, read on and apply today for a life-changing career. As a Sr. Global HEOR Manager at Novo Nordisk, you will be responsible for:Supporting the Health Economics and Outcomes Research strategies and plans to contribute to market access preparedness for pipeline and launch products and to demonstrate the Health Economics and Outcomes Research value of the Novo Nordisk Diabetes products. Provide strategic inputs in market access decision making, address the fundamental payer needs and build economic value arguments to secure reimbursement and broader market access of Novo Nordisk products. Support in driving HEOR strategy for NN Diabetes pipeline products in collaboration with DK team.Support the Diabetes access team in driving team s growth.Demonstrates subject matter knowledge and professional application.Demonstrates project management capabilities in driving projects. Qualifications To be our new Sr. Global HEOR Manager, we are looking for a candidate with the following qualifications: University master s degree in appropriate field such as health economics or outcomes research, epidemiology or statistics/biostatistics. Documented training in health economics or outcomes research.More than six years of experience in health economics and health outcomes research, ideally within pharmaceutical industry or consultancy. Scientific publication track record (in peer-reviewed manuscripts) is preferable.Effective communication skills. Stakeholder management (both within BLR & DK)The Commercial, Global Business Services (GBS) unit is responsible for driving deliverables for multiple Corporate Vice President (CVP) areas within Commercial, GBS, including Insulin, GLP-1 and Obesity Marketing, Market Access, Commercial Planning and Commercial Operations. The Commercial, GBS unit also supports BioPharma global marketing for Hemophilia and growth disorders. Working at Novo Nordisk

Life-changing careers - Check out this open position at Novo Nordisk Senior Global HEOR Manager Job description Job description Are you passionate about driving market access preparedness and demonstrating the value of healthcare products Do you have experience in Health Economics and Outcomes Research We are looking for a Sr. Global HEOR Manager to join our team in Novo Nordisk. If you are ready for a challenging and impactful role, read on and apply today for a life-changing career. As a Sr. Global HEOR Manager at Novo Nordisk, you will be responsible for:Supporting the Health Economics and Outcomes Research strategies and plans to contribute to market access preparedness for pipeline and launch products and to demonstrate the Health Economics and Outcomes Research value of the Novo Nordisk Diabetes products. Provide strategic inputs in market access decision making, address the fundamental payer needs and build economic value arguments to secure reimbursement and broader market access of Novo Nordisk products. Support in driving HEOR strategy for NN Diabetes pipeline products in collaboration with DK team.Support the Diabetes access team in driving team s growth.Demonstrates subject matter knowledge and professional application.Demonstrates project management capabilities in driving projects. Qualifications To be our new Sr. Global HEOR Manager, we are looking for a candidate with the following qualifications: University master s degree in appropriate field such as health economics or outcomes research, epidemiology or statistics/biostatistics. Documented training in health economics or outcomes research.More than six years of experience in health economics and health outcomes research, ideally within pharmaceutical industry or consultancy. Scientific publication track record (in peer-reviewed manuscripts) is preferable.Effective communication skills. Stakeholder management (both within BLR & DK)The Commercial, Global Business Services (GBS) unit is responsible for driving deliverables for multiple Corporate Vice President (CVP) areas within Commercial, GBS, including Insulin, GLP-1 and Obesity Marketing, Market Access, Commercial Planning and Commercial Operations. The Commercial, GBS unit also supports BioPharma global marketing for Hemophilia and growth disorders. Working at Novo Nordisk

The University of Hong Kong Apply now Ref.: 533135 Work type: Full-time Department: School of Public Health (22400) Categories: Research Staff Hong Kong Research Assistant I/II (several posts) in the Division of Health Economics, Policy and Management, School of Public Health (Ref.: 533135), to commence as soon as possible for a one-year temporary term contract, with the possibility of renewal subject to satisfactory performance and funding availability. Applicants should possess a Bachelor's degree or above in health sciences. Knowledge of public health and epidemiology would be a plus. Fresh graduates will be considered for appointment. Strong interpersonal skills, Cantonese and English communication skills are essential to work with parents/caregivers and engage with stakeholders. The applicant should be dependable, detail-oriented and capable of handling project administration. The appointees will participate in research project conducted in partnership with an NGO and supported by a major philanthropic trust. An impact evaluation of a mental support programme for parents/carers of children with special educational needs will be conducted. This programme targets parents/caregivers at risk of depression, anxiety, and stress. The appointees will be primarily responsible for fieldwork for a pragmatic trial. They will conduct data collection from caregivers at various primary and secondary schools in the first two years. Working off-campus may be required. A flexible working schedule may be required on occasion. Other duties may include reports preparation, stakeholder engagement and project management. Enquiries about the duties of the posts should be sent to Professor Jianchao Quan at jquan@hku.hk. A highly competitive salary commensurate with qualifications and experience will be offered, in addition to annual leave and medical benefits. The University only accepts online application for the above posts. Applicants should apply online and upload an up-to-date CV. Review of applications will start as soon as possible and continue until October 31, 2025 , or until the posts are filled, whichever is earlier. Advertised: Sep 11, 2025 (HK Time) Applications close: Oct 31, 2025 (HK Time) Back to search results Apply now Whatsapp Facebook LinkedIn Email App

The University of Hong Kong Apply now Ref.: 533160 Work type: Full-time Department: School of Public Health (22400) Categories: Research Staff Hong Kong Senior Research Assistant or Research Assistant I in the Division of Epidemiology and Biostatistics, School of Public Health (Ref.: 533160) ( to commence as soon as possible on a one-year temporary term contract, with the possibility of renewal subject to funding availability and satisfactory performance) Applicants applying for the Senior Research Assistant position should possess a Bachelor’s degree in epidemiology, biostatistics, public health, statistics, or a related discipline, with at least 3 years of experience; or a Master’s degree with at least 1 year of post-qualification experience; or a Ph.D. degree. They should (i) have solid research experience in communicable and/or non-communicable diseases; (ii) be competent in statistical and programming software packages, such as R, Python, or MATLAB, for data analysis and disease modeling; (iii) have an excellent command of both written and spoken English and Chinese (either Cantonese or Putonghua); and (iv) be organized, responsible, detail-oriented, self-motivated, and able to work independently as well as in a multidisciplinary team. Applicants who possess a Bachelor’s degree in a related discipline but have less experience may apply for the Research Assistant I position. The appointee will lead and support projects on the health economic evaluation of cancer prevention strategies. He/She will also be responsible for conducting systematic literature searches and reviewing clinical data for the projects. He/She will write scientific publications and reports. Working off-campus may be required. Information about the School can be obtained at http://sph.hku.hk. A highly competitive salary commensurate with qualifications and experience will be offered, in addition to annual leave and medical benefits. The University only accepts online application for the above post. Applicants should apply online and upload an up-to-date CV, along with a list of research publications, if any. Review of applications will commence on September 18, 2025, and continue until October 31, 2025 , or until the post is filled, whichever is earlier. Advertised: Sep 11, 2025 (HK Time) Applications close: Oct 31, 2025 (HK Time) Back to search results Apply now Whatsapp Facebook LinkedIn Email App

About the job Our Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. SBO strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally. Main responsibilities: SGH Manager HEVA (BP support) will support Global HEVA business partners (BPs) in execution of multiple HEOR activities: SLR, ITC, Modeling, dossiers, etc. Manage assigned projects in the assigned portfolio in support of the product strategy and value proposition Work with Global HEVA BPs to manage and execute of research projects, economic models, trial design recommendations and other activities in support of programs/products as required Support HEVA BPs in the planning, design, implementation, and completion of innovative evidence-based research programs that are consistent with program/product strategies. The research programs developed by Global HEVA BPs will provide appropriate evidence and/or tools to be used for internal decision making and for external audiences at product launch and over product life cycle Collaborate with Global HEVA BPs to seek opportunities to innovate HEVA value identification, evidence generation and dissemination process/plan to increase the relevance and impact of HEVA evidence to ensure reimbursement decisions optimal access Create complex and specialized strategic content independently Develop and maintain TA expertise Develop and review content created by HEVA associates and cross-functional HEVA hub associates Coach HEVA associates People: (1) Develop and maintain effective relationships with key internal stakeholders including Medical Affairs, Clinical Development, Commercial and Market Access (2) Constantly assist and provide effective feedback to HEVA associates (senior or Junior) in developing knowledge and sharing expertise (3) Work effectively with global HEVA teams across various time zones Performance: (1) Manage the HEVA evidence generation plan in collaboration with Global HEVA BPs (2) Develop research plan to support pre-launch, launch and post-launch evidence for investigational and marketed drugs (3) Evidence generation plan includes burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective and prospective observational studies, economic evaluations, development and analysis of patient-reported outcomes (4) Provide strategic support with individuals and institutions, which may serve as resources for evidence generation purpose, etc. (5) Partner with Global HEVA BPs in execution of approved HEVA studies and tracking of ongoing studies according to budget and timeline expectations (6) Work closely with the HEVA product lead to manage and execute research studies to support the clinical, economic and humanistic value of products (7) Studies include but are not limited to burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective and prospective observational studies, economic evaluations, and patient-reported outcomes (8 )Collaborate with HEVA BPs to set evidence generation priorities and direction for assigned responsibilities and is able to incorporate this into appropriate planning documents (9) Supports Global HEVA BPs in contracting and project management activities pertaining to HEVA studies (10) Works with contracts managers to ensure timely execution of contracts (11) Responsible for tracking and maintaining budget sheet, contracts, SOWs etc. (12) Lead development of core value dossier (CVD) and AMCP dossiers under the strategic direction of Global HEVA BPs Process: (1) Develop complex HEVA strategic evidence material (2) Build expertise in the field of HEVA for the assigned Therapeutic area (3) Manage core HEVA strategic evidence generation processes, templates, and products across the portfolio in accordance to the scientific and value messages aligned with CVD, the US AMCP dossier, and HEVA contributions as appropriate to other submissions (4) Accountable for adherence to the evidence generation guidelines and other standards relevant to HEVA evidence generation processes at SGH (5) Work with selected vendors/SGH within the region to deliver the required deliverables as per defined process as per the business need (6) Leverage advanced training delivery tools & techniques thereby enhancing the effectiveness of training delivery (7) design an overall plan of action basis end-customers feedback & improve course content and delivery Stakeholder: Work closely with HEVA, RWE, Clinical, Medical Affairs, Marketing, External Affairs and Market Access global or local teams in regions/areas to identify evidence generation and dissemination needs and assist in developing assigned deliverables. Liaise with these teams to prepare relevant & customized deliverables and ensure milestones and timelines are on track for assigned the projects About you Experience : 8+ years of experience in HEOR for the pharmaceuticals industry or CRO Strong project management and analytical skills to translate clinical and economic information and messages into payer evidence strategies. Relevant training/ experience in health economics, public health, epidemiology, or other relevant health-related scientific discipline. Soft skills : Demonstrate effective communication, organizational and interpersonal skills. Able to work effectively as part of a multidisciplinary global teams. Able to work independently, but in concert with the direction provided by their management, in accordance with defined functional policies and precedents, budgetary guidelines, company values, ethics and applicable law. Ability to handle multiple projects across different therapeutic areas. Strong customer focus. Ability to work well in a cross-functional team. Understanding of the disease environment and the evolution of the market access landscape and implications for the business. Proven track record working successfully in a project/matrix-oriented environment. Excellent communication skills and ability to understand and present complex information in digestible ways for internal (e.g. senior management) and external audiences. Strong team spirit, sense of transversality, multicultural awareness, and ability to drive matrix teams. Technical skills : Robust understanding of reimbursement decisions to determine value drivers and how evidence is used in decision making and how it impacts various payers (e.g., providers, patients, health systems). Strong knowledge of methods and principles of health economics, health technology assessment (HTA) reviews. Strong ability to systematically review available scientific evidence to identify clinical needs of the payer. Understands, creates, and applies relevant methods (e.g., observational data, post hoc analysis of clinical trials, meta-analysis, indirect comparison, etc..) to demonstrate product value potential and drives processes around the same Education : Advanced degree in life sciences/ pharmacy/ similar discipline or medical degree Languages : Excellent knowledge of English language (spoken and written) Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! null

Position Summary: The Professor of Community Medicine is a senior academic role responsible for leadership in teaching, research, public health outreach, and departmental administration. The candidate will ensure high-quality education for undergraduate and postgraduate students while actively engaging in research, policy advocacy, and community health initiatives in alignment with national and institutional goals. Key Responsibilities: Teaching & Academics Deliver lectures, practicals, and fieldwork sessions for MBBS and MD (Community Medicine) students. Design, update, and implement curriculum as per NMC (National Medical Commission) guidelines. Supervise PG dissertations and guide students in academic writing and publication. Lead academic audits, exam preparation, and assessment processes. Mentor junior faculty, interns, and postgraduate residents. Research & Publications Lead and collaborate on departmental and interdisciplinary research projects. Publish a minimum number of original research papers in indexed national/international journals as per NMC criteria. Secure research funding through ICMR, WHO, or government-funded projects. Promote evidence-based practice in public health. Public Health & Community Outreach Supervise and coordinate activities at Urban and Rural Health Training Centres (UHTC/RHTC) . Organize health camps, disease surveillance, immunization drives, and IEC/BCC campaigns. Collaborate with government health departments, NGOs, and local communities for impactful outreach. Train students in the application of epidemiology, biostatistics, and health education. Administration & Leadership Head the Department of Community Medicine and oversee daily operations. Manage departmental resources, teaching schedules, and faculty/staff development. Represent the department in institutional committees and accreditation processes (NMC, NAAC, NABH). Contribute to strategic planning, quality assurance, and interdepartmental collaboration. Qualifications: Educational: MBBS from a recognized medical institution. MD / DNB in Community Medicine (Preventive and Social Medicine). Experience: Minimum 10 years of teaching experience post-MD. At least 4 years as Associate Professor in Community Medicine. Minimum 4 research publications , with at least 2 as first/corresponding author during Associate Professorship (as per NMC norms). Qualification - MBBS, MS/MD, DNB Eligibility - As per NMC Norms Speak with employer : 9342175715 / 9131856296 Mail Id : esidiwagar@gmail.com / elevatedsynergyindia@gmail.com Job Type: Full-time Pay: ₹150,000.00 - ₹250,000.00 per month Work Location: In person

About Healing Fields Foundation Healing Fields Foundation is a non-profit organization with a mission to b uild an eco-system that ensures access to affordable and quality healthcare for all, especially women from rural and resource-poor communities. Through our health management expertise, training and research methodology, we support organizations and people involved in the development and delivery of the entire healthcare ecosystem. We work in close partnership with community, service organizations, private agencies, government and semi-government sectors, and focus on access and affordability to quality health care as our primary objective. For further details on the organization’s work, please visit the website www.healing-fields.org Position: Monitoring and Evaluation Data Storytelling Associate We are looking for a skilled and strategic Monitoring and Evaluation (M&E) Data Storytelling Associate to join our team, bringing a strong focus on data communication, collaboration, and using data for strategic insight. In this role, you will support verbal and written communication of data generated through the monitoring and evaluation processes to amplify program impact and communicate outcomes effectively. You will also anchor external collaborations that utilise technology to improve data collection and analysis. This position requires a mix of analytical skills, storytelling capabilities, creative thinking around the use of technology, and a collaborative spirit, working closely with internal teams and external partners to ensure that data-driven insights guide our initiatives and reach our stakeholders. Key Responsibilities: Data Storytelling & Reporting: Craft compelling narratives from data insights to communicate in verbal and written mediums the organization’s impact to various audiences, including donors, partners, and community stakeholders. Develop visually engaging content such as infographics, case studies, and multimedia stories to highlight key program achievements. External Representation & Partnerships: Represent the organization in external forums, specifically in M&E working groups, donor meetings, and strategy sessions, sharing program impact and key learnings. Engage with internal stakeholders to align on M&E metrics, address data requirements, and ensure mutual goals are met. Build and maintain relationships with stakeholders, acting as a bridge between senior management, program implementation teams and external collaborators. Innovation and Technology Partner with external experts to introduce cutting-edge innovations and best practices in data capture and analysis. Stay updated on industry trends, particularly those intersecting rural health and technology. Bridge grassroots needs with technological advancements to deliver impactful, context-specific solutions. Strategic Planning & Capacity Building: Contribute to organizational goals by synthesizing data insights into actionable recommendations for program improvement and expansion. Provide training and support to all staff on M&E tools and storytelling techniques, fostering a culture of learning and data-driven decision-making. Promote the use of adaptive learning approaches by encouraging dialogue on evaluation findings and innovative solutions. Qualifications: Bachelor’s degree in Social Sciences, International Development, Communications, Epidemiology, Statistics, Public Policy, or related field (Master’s preferred). Minimum 3 years of experience in M&E, program evaluation, or impact assessment in a non-profit or NGO setting. Strong analytical thinking, with a talent for translating complex data into actionable insights. Excellent communication and storytelling skills, including the ability to present data in a compelling and accessible way. Experience with data visualization tools and software (e.g., Tableau, Power BI) is a plus. Proficiency in M&E methodologies and tools, with familiarity in managing databases and data analysis software. Collaborative team player who can effectively engage with diverse stakeholders. High level of initiative, with a proactive approach to problem-solving and innovation. Commitment to the mission and values of the organization, with a passion for health impact and sustainable development. This role offers an exciting opportunity to contribute to our mission by enhancing data-driven decision-making and amplifying our impact through effective communication and collaboration. Please email CV to hrd@healing-fields.org

Department: Global Health Economics & Outcomes Research (HEOR) Job Family: Health Economics Job Type: Full-Time Location: Hyderabad, India Reports To: Global Systematic Literature Review Team Lead Position Summary The Global Systematic Literature Review (SLR) Manager provides expertise in designing, executing, and managing literature review services within Amgen’s Global HEOR function. The SLR Manager will collaborate closely with Global HEOR Product Leads to align with HEOR product strategy. This role supports global access to Amgen's therapies through the generation of high-quality, evidence-based outputs across the product lifecycle. Key Responsibilities Refine literature review questions in alignment with Global HEOR Product Lead and prepare research protocols. Develop inclusion/exclusion criteria within the PICO framework. Design literature searches for electronic databases (e.g., PubMed, EMBASE, Cochrane Library) and grey literature (e.g., conference proceedings, regulatory sites). Screen abstracts and full-texts to determine relevance based on PICO criteria. Create and review PRISMA diagrams to document full-text study selection. Develop and validate data abstraction tools; finalize analyzable datasets. Draft evidence tables, figures, final reports, and presentation decks, interpreting patterns and trends. Manage project timelines and deliverables. Conduct training and onboarding for literature review tools and platforms. Experience of working with literature review platforms and AI tools Knowledge and experience of conducting meta-analyses People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEOR teams across various time zones Qualifications Education Bachelor’s or Master’s degree in pharmacy, health economics, public health, medicine, epidemiology, or a related health sciences field. Experience Years of relevant experience in systematic literature review methods in the pharmaceutical, biotech or consulting setting: +6 years for Master’s degree and +8 years for Bachelor’s degree. Experience in evidence synthesis feasibility assessments and network meta-analysis is preferred. Proficiency in biomedical databases (e.g., MEDLINE, Embase). Strong understanding of research principles and implementation. Skills & Competencies Excellent English oral and written communication, with ability to tailor content to different stakeholders; past medical writing experience is a plus Skilled with EndNote or other reference management tools (preferred). Proficiency with Microsoft Office (Word, PowerPoint, Excel). Experience on systematic review tools and citation databases (e.g., PubMed, EMBASE); High attention to detail and strong editing/fact-checking abilities. Innovative use of artificial intelligence to boost efficiency Organizational Behaviors Team-oriented with demonstrated collaboration. Capable of managing multiple projects simultaneously. Comfortable working in a global team across time zones and cultures.

Department: Global Health Economics & Outcomes Research (HEOR) Job Family: Health Economics Job Type: Full-Time Location: Hyderabad, India Reports To: Global Systematic Literature Review Team Lead Position Summary The Global Systematic Literature Review (SLR) Senior Associate provides expertise in designing, executing, and managing literature review services within Amgen’s Global HEOR function. The SLR Senior Associate will collaborate closely with team lead and Global HEOR Product Leads to align with HEOR product strategy. This role supports global access to Amgen's therapies through the generation of high-quality, evidence-based outputs across the product lifecycle. Key Responsibilities Refine literature review questions in alignment with team lead and prepare research protocols. Design literature searches for electronic databases (e.g., PubMed, EMBASE, Cochrane Library) and grey literature (e.g., conference proceedings, regulatory sites). Screen abstracts and full-texts to determine relevance based on PICO criteria. Create and review PRISMA diagrams to document full-text study selection. Extract data from included articles into a predefined data extraction template Draft evidence tables, figures, final reports, and presentation decks, interpreting patterns and trends. Ensure quality of assigned work People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEOR teams across various time zones Qualifications Education Bachelor’s or Master’s degree in pharmacy, health economics, public health, medicine, epidemiology, or a related health sciences field. Experience Years of relevant experience in systematic literature review methods in the pharmaceutical, biotech or consulting setting: +3 years for Master’s degree and +5 years for Bachelor’s degree. Experience of conducting different types of literature reviews (clinical, economic, QoL, burden of illness etc.) Able to prioritize and manage multiple projects with high efficiency in first pass, second pass and data extraction milestones Proficiency in biomedical databases (e.g., MEDLINE, Embase). Strong understanding of research principles and implementation. Skills & Competencies Excellent English oral and written communication, with ability to tailor content to different stakeholders; past medical writing experience is a plus Skilled with EndNote or other reference management tools (preferred). Proficiency with Microsoft Office (Word, PowerPoint, Excel). Experience on systematic review tools and citation databases (e.g., PubMed, EMBASE); High attention to detail and strong editing/fact-checking abilities. Innovative use of artificial intelligence to boost efficiency Organizational Behaviors Team-oriented with demonstrated collaboration. Capable of managing multiple projects simultaneously. Comfortable working in a global team across time zones and cultures.

Global HEOR Systematic Literature Review Senior Associate Department: Global Health Economics & Outcomes Research (HEOR) Job Family: Health Economics Job Type: Full-Time Location: Hyderabad, India Reports To: Global Systematic Literature Review Team Lead Position Summary The Global Systematic Literature Review (SLR) Senior Associate provides expertise in designing, executing, and managing literature review services within Amgen’s Global HEOR function. The SLR Senior Associate will collaborate closely with team lead and Global HEOR Product Leads to align with HEOR product strategy. This role supports global access to Amgen's therapies through the generation of high-quality, evidence-based outputs across the product lifecycle. Key Responsibilities Refine literature review questions in alignment with team lead and prepare research protocols. Design literature searches for electronic databases (e.g., PubMed, EMBASE, Cochrane Library) and grey literature (e.g., conference proceedings, regulatory sites). Screen abstracts and full-texts to determine relevance based on PICO criteria. Create and review PRISMA diagrams to document full-text study selection. Extract data from included articles into a predefined data extraction template Draft evidence tables, figures, final reports, and presentation decks, interpreting patterns and trends. Ensure quality of assigned work People: (1) Support and maintain effective relationships with key stakeholders (2) Work effectively with global HEOR teams across various time zones Qualifications Education Bachelor’s or Master’s degree in pharmacy, health economics, public health, medicine, epidemiology, or a related health sciences field. Experience Years of relevant experience in systematic literature review methods in the pharmaceutical, biotech or consulting setting: +3 years for Master’s degree and +5 years for Bachelor’s degree. Experience of conducting different types of literature reviews (clinical, economic, QoL, burden of illness etc.) Able to prioritize and manage multiple projects with high efficiency in first pass, second pass and data extraction milestones Proficiency in biomedical databases (e.g., MEDLINE, Embase). Strong understanding of research principles and implementation. Skills & Competencies Excellent English oral and written communication, with ability to tailor content to different stakeholders; past medical writing experience is a plus Skilled with EndNote or other reference management tools (preferred). Proficiency with Microsoft Office (Word, PowerPoint, Excel). Experience on systematic review tools and citation databases (e.g., PubMed, EMBASE); High attention to detail and strong editing/fact-checking abilities. Innovative use of artificial intelligence to boost efficiency Organizational Behaviors Team-oriented with demonstrated collaboration. Capable of managing multiple projects simultaneously. Comfortable working in a global team across time zones and cultures.

Job Description Position: Medical Coder Ct: HR HR Shanmugapriya - 8072891550 Medical Coding is the process of converting patient health information into alpha numeric codes. Coders take medial reports from doctors, which may include a patients condition, the doctors diagnosis, a prescription, and whatever procedures the doctor or healthcare provider performed on the patient, and turn that into a set of codes, which make up a crucial part of the medical claim. Eligibility All (UG/PG) Life Science Paramedical Graduates BDS BPT BHMS BAMS Siddha,Unani,Naturopathy {Dip Bsc Msc} Nursing/GNM {B.E M.E} Biomedical Engineering {B.tech,M.tech}Biotechnology Biochemistry Bioinformatics Microbiology Zoology and Advanced zoology Biology Botany Medical Lab Tech Plant biotechnology Pharmacy(B.Pharm M.pharm) Paramedical Physiotherapy Physician assistant Critical Care Technology Medical Biochemistry Medical Record Science Operation Theatre Anaesthesia Technology {Bsc Msc Dip} Clinical Nutrition Human Genetics Medical Laboratory Technology Medical Sociology Epidemiology Molecular Virology Biostatistics Blood Banking Technology Regenerative Medicine Optom. Genetic Counseling Radiology Imaging Technology Medical Biochemistry Medical Microbiology Clinical Care Technology Clinical Care Technology Medical Physics {Bsc Msc Dip} Accident Emergency Care Technology Audiology speech Language Pathology Cardiac Technology Cardio Pulmonary Perfusion Care Technology Critical Care Technology Dialysis Technology Neuro Electrophysiology Medical Sociology Nuclear Medicine Technology Operation Theatre Anaesthesia Technology Optometry Physician Assistant Radiology Imaging Technology Radiotherapy Technology Medical Record Science Respiratory Therapy Fitness and Lifestyle Modifications Accident Emergency Care Technology Critical Care Technology Nursing Aide Operation Theatre Anesthesia Technology Ophthalmic Nursing Assistant Medical Record Science Optometry Technology Radiology Imaging Technology Medical Lab Technology Cardiac Non Invasive Technology Dialysis Technology Dentist Requirement Knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills Benefits System based job Weekly 5 days duty Day shift with Sat and Sun off Food and Cab provided by company Incentives based on performance Starting salary 12k to 25k with increment in 6 months for experienced. Abroad opportunities available Bonus for referring friends Medical expenses covered by company Provident Fund will be provided Gratuity after 5 yrs of work experience. Job Location: Chennai, Coimbatore, Vellore, Trichy, Cuddalore, Pondi Salem, Erode, Namakkal, Thanjavur, Nagercoil, Theni,Dindokal Thiruvannamalai, Villupuram, Karur, Tirunelveli,Kanniyakumari Tirupati, Kerala, AP,Tamilnadu,Telangana Ct: HR HR Shanmugapriya - 8072891550 This job is provided by Shine.com

This job is based in Australia. The role is a full-time position requiring 35 hours per week on a 2-year fixed-term contract. The remuneration for this position is at Level C, ranging from $155k to $178k base salary, plus 17% Superannuation and Annual Leave Loading. Visa sponsorship is available for this position, and the location is at Randwick Clinical Campus, Sydney NSW. The Population Child Health (PCH) Research Group, based at the University of New South Wales (UNSW) Randwick precinct and Sydney Children's Hospitals Network (SCHN), is an integrated, multidisciplinary clinical research team. Their focus is on conducting translational health services and health systems research to optimize child health outcomes and address inequities, particularly for priority populations, integrating care, and emphasizing the first 2000 days. The Senior Research Fellow, Child Health Services Research, is expected to play a pivotal role in advancing child health research within the PCH Research Group, UNSW. The ideal candidate should possess leadership qualities, drive research strategy, foster collaboration, and achieve impactful outcomes. Responsibilities include contributing to high-quality publications, securing competitive grants, and forming partnerships to enhance health service delivery and outcomes for children and young people. This role involves working closely with diverse stakeholders, including clinicians, health services, policymakers, academic partners, and providing mentorship where necessary. Candidates for this position should hold a PhD in health services research, epidemiology, psychology, or non-lab-based child health research. A proactive approach to staying updated with discipline knowledge, a strong track record in research, and the ability to achieve research excellence and leadership are essential. Experience in translational intervention research is preferred, along with the capability to secure grant income. Collaboration skills, interpersonal abilities, organizational proficiency, and a commitment to UNSW's objectives and values are crucial. Knowledge of health and safety responsibilities is required, along with a willingness to attend relevant health and safety training sessions. Pre-employment checks for this position include verifying qualifications, obtaining a Working with Children Check (WWCC), and a Criminal Records Check. UNSW offers benefits such as 17% Superannuation and leave loading, flexible working arrangements, additional leave over the Christmas period, access to lifelong learning and career development opportunities, and progressive HR practices. To apply for this position, interested candidates should click on "Apply now" to submit their application online. Resumes and a separate document addressing the main skills and experience outlined in the position description are required. The Position Description can be accessed on JOBS@UNSW. For process-specific queries, contact Anabel Wason, the Talent Acquisition Consultant, at a.wason@unsw.edu.au. The application deadline is Tuesday, 30th September 2025, at 11:55pm (Sydney time). Applications should be submitted through the application portal and not sent to the provided contacts. UNSW is dedicated to equity, diversity, and inclusion. Candidates from various backgrounds, including women, individuals from culturally and linguistically diverse communities, those with disabilities, members of the LGBTIQ+ community, and people of Aboriginal and Torres Strait Islander descent, are encouraged to apply. The University offers workplace adjustments for individuals with disabilities and provides flexible work options for eligible staff. Please note that the University reserves the right not to proceed with any appointment.,