We require doctors for Medical Colleges & Hospitals PAN India Qualification: MD/MS, DNB, (All Department) Position: Consultant, SR, AP, Associate Professor, Professor Department: Clinical & Non Clinical Mamta Call/WhatsApp: 8708568683 weps.placement@gmail.com

Mahatma Gandhi Mission Hospital is looking for Pharmacologist to join our dynamic team and embark on a rewarding career journey. Conduct research on the effects of drugs and other chemical substances on biological systems, including mechanisms of action, therapeutic uses, and side effects.Design, plan, and oversee laboratory experiments using various in vitro and in vivo models to evaluate efficacy, pharmacokinetics, and toxicology of new compounds.Analyze and interpret experimental data to draw conclusions on drug behavior and suitability for further development.Collaborate with interdisciplinary teams including chemists, biologists, and clinicians to develop new medications and treatment protocols.Prepare technical reports, scientific publications, and regulatory documentation to support drug approval processes.Ensure adherence to ethical guidelines, safety standards, and compliance regulations in all research and testing.Stay updated on advancements in pharmacological science and integrate emerging technologies into ongoing research projects.Mentor junior researchers and provide expertise in drug development and clinical pharmacology.

Role & responsibilities Clinical Pharmacologist Preferred candidate profile Pharm. D

Need Assistant Prof Pharmacology For Best Medical College in UP. Education :- MD / DNB Experience :- 1 - 3 Years Salary :- 1.7 - 1.8 LPM Email :- hrtps006@gmail.com Contact :- 7300634604

We are looking for a highly motivated and target-driven Territory Manager to promote and sell our pharmaceutical products to doctors, clinics, and hospitals. The role involves building strong customer relationships, increasing product awareness, and achieving sales goals in the assigned territory. Key Responsibilities: • Promote and sell the company’s pharmaceutical products to doctors, healthcare professionals, and chemists. • Schedule and conduct meetings with medical professionals to present product information and therapeutic benefits. • Build and maintain strong relationships with existing clients while identifying and developing new business opportunities. • Achieve monthly, quarterly, and annual sales targets set by the management. • Ensure proper product availability in pharmacies and hospitals. • Provide feedback on competitor activities, market trends, and customer insights. • Maintain accurate records of daily calls, visits, and sales reports Requirements: • Bachelor’s degree in Pharmacy, Life Sciences, or any related field (preferred). • Proven experience in medical or pharmaceutical sales (1–3 years preferred, but freshers may also apply). • Strong interpersonal, communication, and negotiation skills. • Good knowledge of human anatomy, pharmacology, and therapeutic classes. • Ability to work independently and manage time effectively. • Willingness to travel within the assigned territory. Why Join Us? Competitive Salary & Incentive with tremendous growth opportunitiesTraining and development opportunitiesSupportive and dynamic work environment

Hi We are hiring for ITES Company Role -Medical Reviewer Qualification : MBBS/MD only (MCI Certification is not mandate**) Experience Range : 1 to 7 Years Preferred Experience: Minimum of 1 years of experience in PV/ Clinical Research (drug safety) Job Description: Author a company clinical comment (CCC) for case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Edit the Periodic Report Comment, if applicable, directly within the Periodic Report Comment field in the Patient Safety database. Perform the following actions within the Comments field of the GSP Review Workflow step in the Patient Safety database: -Review and respond to any queries/comments from the Case Owner, which are recorded in the Comment field of the GSP Review Workflow step in the Patient Safety database. -Detail any requests for changes to the case, including the narrative. -Detail any follow-up information that is required and not already noted within the Query Manager in the Patient Safety database. Provide product advice as required, especially with regards to case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Review the company causality assessment provided by Medical Advisor. • Review the medical sense including seriousness and coding of the case in the global context of the drug or clinical project, including the narrative, AE/SAE terms, suspect drugs, concomitant medications, laboratory data, and medical history. To provide documentation of the review and case comments in Sapphire in Medical Review workflow. Maintain knowledge of the marketed drug currently under litigation. Maintain knowledge of the company disease and therapeutic areas for marketed drugs and drugs in development through periodic medical review training held by client medical staff. Skills required: Computer Literate (good knowledge of MS Office) Sound understanding of the Drug Safety and Regulatory process Good problem solving and decision-making skills Capability to lead by motivation and example Ability to prioritize schedule and organize Excellent interpersonal and communication skills To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Medical Reviewer Mumbai (Job Code # 47) b) For Position in Pune Search : Medical Reviewer Pune (Job Code # 48) c) For Position in Bangalore Search : Medical Reviewer Bangalore (Job Code # 51)

Hi We are hiring for the leading ITES Company for the Medical Reviewer Role. Qualification - MBBS/MD is Must (Full TIme) Job Overview: The Medical Reviewer is responsible for the evaluation and analysis of clinical data to ensure accuracy, compliance with regulations, and the highest quality standards. This role involves reviewing clinical trial data, medical documentation, and regulatory submissions to support the approval of new medical products and therapies. Key Responsibilities: Clinical Data Review : Evaluate clinical trial data for completeness, accuracy, and adherence to protocols. Ensure data integrity and consistency across various documents and databases Medical Documentation: Review and verify the accuracy of medical documentation, including patient records, case reports, and clinical study reports. Ensure documentation complies with regulatory requirements and company standards. Regulatory Compliance: Stay updated with the latest regulatory guidelines and ensure all reviews align with current regulations. Prepare and review regulatory submissions to ensure timely and successful product approvals. Training and Development: Stay informed about advancements in medical research and regulatory changes. Participate in continuous training and development programs to enhance knowledge and skills. Skills required: Computer Literate (good knowledge of MS Office) Sound understanding of the Drug Safety and Regulatory process Good problem solving and decision-making skills Capability to lead by motivation and example Ability to prioritize schedule and organize Excellent interpersonal and communication skills To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Chennai Search : Medical Reviewer Chennai (Job Code # 52) b) For Position in Indore Search : Medical Reviewer Indore (Job Code # 53)

MD Emergency Medicine Required at Azamgarh UP Salary 3 to 3.5 Lakhs + Accommodation Couple can be placed in their respective branch OR We can also help you to find out suitable job as per your preferred location

Anaesthesiologist Required Azamgarh UP Mainly for ICU 3 Candidates Required Salary 3 to 3.5 Lakhs Sonipat Haryana For ICU IDCCM Preferred Salary Rs. 3 to 4 Lakhs Gurgaon Haryana Salary 2 Lakhs + Share Required Candidate profile Goalpara, Assam Salary: 3 - 3.5 Lakhs + Accommodation Neemrana, Rajasthan Salary: 3 - 4 Lakhs + Accommodation Bhiwani Haryana Salary 2.5 to 3 Lakhs + Accommodation

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a part of the Jubilant Pharmova family of companies with R&D centres in India and business offices in Asia and North America. With our global reach, Jubilant Biosys provides comprehensive drug discovery services and contract research services–from target discovery to candidate selection and with flexible business models (FFS, FTE and risk shared)–in partnership with leading worldwide healthcare companies. With a clear scientific focus in oncology, metabolic disorders, central nervous system (CNS) diseases, pain and inflammation, Jubilant Biosys has rapidly emerged as a leading collaborator for pharmaceutical and biotechnology companies worldwide. In each of these therapeutic areas, Jubilant Biosys has developed a deep level of expertise in discovery informatics, computational chemistry , medicinal chemistry, structural biology , biology,in-vivo,in-vitromodels and translational sciences. Combined with strong clinical development and manufacturing capabilities from other Jubilant subsidiaries, Jubilant Biosys has risen as a fully integrated contract research organization in India and headquartered at Bengaluru with end-to-end solutions. Our ability to be the preferred collaborator in the drug discovery domain is sustained by our commitment to comply with and continually improve our quality systems and to provide the following services: Contract Research Preclinical CRO Drug Discovery Virtual Screening Protein Crystallization Toxicology &In-vitroADME Medicinal Chemistry Synthetic & Developmental Chemistry Pharmacology Jubilant Biosys collaborates with the world’s leading pharmaceutical, biotech companies, academic institutions and research foundations. Find out more about us at www.jubilantbiosys.com The Position Organization : - Jubilant Biosys Designation & Level : - RA Location: - Greater Noida Department: - Analytical Key Responsibilities Having exposure of 1-4 years in analytical chemistry, method development and analysis of regular samples on chromatographic instruments (LC-MS). Candidate should be well acquainted with the respective instrument and software. Maintenance, cleaning, documentation and calibration of analytical instruments. Demonstrate perseverance, team co-ordination and analytical approach at the work place. Should be flexible with working hours. Provide training to new joiners. Practice safe work habits including complying with all safety health and environmental rules and regulations Person Profile Qualification: - M. Sc. (Analytical Chemistry)/ M. Pharm or related field from reputed university/institute. Experience: - 1-4 years of relevant experience for Masters. Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances.

We need MBBS, MD( Pharmacology). Degree completed in INDIA only can apply free hostel only pay for food Immediate joiner Timinig 8.30 to 3.00 travels availabe anywhere 2nd 4th saturday weekoff Job Types: Full-time, Permanent, Fresher Pay: ₹100,000.00 - ₹140,000.00 per month Benefits: Flexible schedule Food provided Health insurance Leave encashment Paid sick time Provident Fund Schedule: Day shift Monday to Friday Morning shift Night shift Rotational shift Supplemental Pay: Performance bonus Quarterly bonus Yearly bonus Work Location: In person

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. The Medical Information Specialist (MIS) position is part of the ProPharma Medical Information Contact Center and follows all corresponding regulations, industry standards, and client/internal policies regarding medical information and the collection and documentation of adverse events, special situation events, and product complaints. Essential Functions Include:Medical Information service delivery Responds to unsolicited consumer, health care professional and other external customer requests for medical and safety information received via telephone, website/e-mail, letter, fax, and scientific meetings on behalf of ProPharma’ s pharmaceutical clients. Provides labeled and unlabeled medical/safety information responses in accordance with regulatory requirements, industry standards and client and ProPharma internal policies and practices. Accurately identifies, documents and reports adverse events, pregnancy reports, special situation events and product complaints in a clear and concise manner per government regulations, ProPharma Standard Operating Procedures (SOPs) and client Working Practices (WPs). Ensures tasks are completed within the deadlines documented in the agreed ProPharma SOPs and WPs. Formulates and provides accurate responses utilizing approved labeling and company standard responses, published literature and other data. Assists with writing custom medical information responses utilizing this data. Logging all enquiries handled in an accurate, comprehensive, and timely fashion into Inquiry Handling Systems. Quality Assurance Maintains quality in all areas of the job, including performing quality checks on Adverse Events, Product Quality Complaints, correspondence, and enquiries logged into the Inquiry Handling Systems General Provides after-hours coverage on a rotated basis subject to business requirements. Adheres to company and country-specific privacy policies, ensuring any confidential information or personal data related to ProPharma and its clients is managed in accordance with Data Privacy regulations described in ProPharma SOPs and the Confidentiality Statement within the Contract of Employment. Complies with the Company’s health and safety policies. Other activities as assigned as delegated by the Manager. Qualified Candidates Must Have Life science degree OR Nursing degree (RN/BS/BA/MS) OR Pharmacy degree Excellent verbal and written communication skills, including proofreading, professional telephone etiquette and empathetic customer service skills. Ability to write in a fluent and grammatically correct manner in the target language for the role English language proficiency. Japan-based roles only: TOEIC 800= Working knowledge of medical terminology, pathophysiology, pharmacology, regulations and industry standards. Strong cognitive abilities, including verbal reasoning, critical thinking and analytical ability. Ability to multitask with attention to detail within restrictive timeframes, including sound planning, prioritizing and organizational skills. Proactive with demonstrative ability to independently identify problems and suggest effective solutions. Ability to learn, take instruction and apply to daily operations/tasks. Receptive to constructive feedback and able to take responsibility for work allocated. Self-motivating. Ability to demonstrate initiative and internal drive. Willingness to seek out additional workload projects. Effectively work independently and as part of a team. Highly proficient in computer applications, including Microsoft Office software platforms and Adobe Acrobat, and experience using a document management system. Aptitude to learn other computer systems including inquiry handling database. We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed. ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

Retail Pharmacist: Saince HealthTech (SHT) is the India subsidiary of Saince Inc., USA. SHT is located in Hyderabad, TS, India. Saince Inc. is an award-winning provider of healthcare solutions with 95% customer satisfaction rating among hospitals and physicians. Saince has been identified as one of the fastest growing private companies in the nation. We currently serve hundreds of hospitals coast to coast in USA. Pharmacist: Dispensing prescription medications accurately and efficiently. Overseeing inventory management and ordering pharmaceutical supplies. Ensuring compliance with all pharmacy laws, regulations, and standards. Maintaining accurate and up-to-date patient records and medication profiles. Maintaining statistical and financial records. Requirements: Bachelor's or Masters of Pharmacy or (Pharm.D.) degree from an accredited pharmacy program Active pharmacy license in Telangana Ability to work effectively in a fast-paced environment and handle multiple tasks. Strong knowledge of pharmaceuticals, pharmacology, and pharmacy operations Excellent communication and interpersonal skills. Attention to detail and accuracy. Commitment to providing outstanding customer service. Flexibility to work in shifts. Perks and Benefits Some of the benefits we provide to our team include: Medical insurance for family including parents (optional) Flexible work hours 20 days paid vacation with leave encashment 4 days per year Volunteering paid days off Annual health and wellness screening Outpatient medical expenses discounts Tuition and certification reimbursement Employee wellness programs Job Types: Full-time, Permanent Pay: ₹9,690.00 - ₹26,334.79 per month Benefits: Health insurance Provident Fund Schedule: Morning shift Education: Bachelor's (Preferred) Experience: Basic computer: 3 years (Preferred) Work Location: In person

Job Title : Associate Professor / Professor Department : College of Pharmaceutical Sciences Institution : Rama University , Kanpur Location : Mandhana , Kanpur Position Type : Full-Time role Position Summary The College of Pharmaceutical Sciences at Rama University seeks a dynamic and dedicated individual for the position of Associate Professor/Professor in the Department of Pharmaceutical Sciences. The successful candidate will have a strong academic background, a passion for teaching, and an active research agenda that will contribute to the growth of the department. This is an exciting opportunity to work in a highly collaborative environment with world-class faculty and contribute to advancing pharmaceutical science education, research, and practice. Key Responsibilities Teaching and Curriculum Development : Teach undergraduate, graduate, and professional courses in Pharmaceutical Sciences, including but not limited to pharmacology, pharmaceutics, medicinal chemistry, and pharmaceutical biotechnology. Develop, implement, and evaluate course content, lecture materials, and assessments. Mentor and advise students, including supervising graduate students in their research projects and theses. Participate in curriculum development and improvement within the department to ensure the program meets the latest advancements in pharmaceutical sciences. Research and Scholarship : Establish and maintain an active research program in an area of pharmaceutical sciences. Publish research findings in peer-reviewed journals and present at national and international conferences. Seek external funding through grants and partnerships to support research initiatives. Collaborate with colleagues within the department and across disciplines to foster research innovation and advancement. Service and Leadership : Contribute to the development of the departments goals, strategic plans, and initiatives. Serve on departmental, college, and university committees as assigned. Participate in professional organizations and activities related to pharmaceutical sciences. Provide leadership in service learning and outreach activities within the community and the profession. Administrative and Professional Development : Participate in academic advising and student recruitment. Attend departmental meetings and contribute to the administrative responsibilities of the department. Engage in ongoing professional development to stay current in the field and contribute to the advancement of pharmaceutical sciences. Required Qualifications Ph.D. in Pharmaceutical Sciences, Pharmacology, Medicinal Chemistry, Pharmaceutics, or a closely related field from an accredited institution. For Associate Professor: A minimum of [X] years of post-doctoral academic and/or professional experience, with a strong track record in teaching, research, and service. For Professor: A minimum of [X] years of post-doctoral academic and/or professional experience, with demonstrated leadership in research, teaching, and professional service. Demonstrated expertise in one or more areas of pharmaceutical sciences (e.g., drug development, pharmacology, medicinal chemistry, clinical pharmacology, pharmaceutics, etc.). A strong record of peer-reviewed publications and external research funding. Experience in teaching at the undergraduate or graduate level, including course development and delivery. Strong communication skills and the ability to mentor students and collaborate with colleagues. Preferred Qualifications Post-doctoral experience in a relevant area of pharmaceutical sciences. Experience in obtaining federal, industry, or foundation research funding. Evidence of leadership in professional organizations, research teams, or educational initiatives. Experience in interdisciplinary collaboration and industry partnerships.

Job description: Cactus Life Sciences is a remote-first organization, and we embrace an "accelerate from anywhere culture". You may be required to travel to our Mumbai office based on business requirements or for company/team events. If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you. Job responsibilities: Use scientific expertise to develop (write, proofread, and data-check) high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client needs with excellent attention to detail under the guidance of the scientific leads. Liaise and build trusting and professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders, including authors, reviewers, and key opinion leaders across therapeutic areas - learning to anticipate their needs. Effectively and proactively communicate with team members, authors/faculty, clients, and vendors. Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives. Attend client and other external meetings and support senior team members as needed. Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans. Ensure all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date. Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines. Share best practices and client preferences, thereby contributing to skill development within the medical communications team. #LI-Remote Qualifications and prerequisites: 1-3 years of experience in relevant fields of scientific writing. PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD with a good understanding of clinical research and medical communication. Should have experience working on publications. Experience working on gastric cancer publications would be preferable. Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills. Excellent communication skills, especially with the clients. Ability to adapt writing style to different materials and target audiences. Basic knowledge of biostatistics. Literature reviewing and evaluation capabilities. Very good working knowledge of MS Office. Application process: Before applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds. For this role, the process will include two Technical Interviews with the Hiring Managers, and a Technical Assessment, where candidates will have agreed upon timeline to complete the task. The final round will be the HR Interview. All interactions will be conducted virtually via MS Teams. Equal Opportunity Our hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic. Accelerating from Anywhere As a remote-first organization, these are essential attributes we look for in all our candidates. Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently. Documenting work that brings everyone on the same page. Maturity to choose between synchronous and asynchronous collaboration. Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status. About Us: At Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do. Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.

Summary The Associate Medical Expert in TCO (Translational Clinical Oncology), is the medical leader for assigned global, roll-over and long-term follow-up studies, and studies in the close-out phase. They may also provide medical support for assigned aspects of a global, active, TCO study, under the leadership of a Clinical Program Leader (CPL) and / or Medical Expert TCO (Translational Clinical Oncology) is a department under Biomedical Research division, and is responsible for designing and executing out early phase (first in human) clinical studies in patients with cancer. It acts as a bridge between drug discovery and late phase clinical development and strives to deliver transformative new medicines for oncology conditions. About the Role Major accountabilities: Provides medical support to Clinical Program Leader (CPL) and / or Medical Expert. Medical support may include, but is not limited to, contributing to clinical sections of protocols and/or amendments, Informed Consents, publications, regulatory documents such as Investigator Brochures, responses to Health Authority questions and conducting ongoing review of clinical trial data, with oversight of TCO deliverables. May act as the medical monitor to support overall program safety reporting (e.g., Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with Patient Safety Team. Contributes to clinical/scientific elements of TCO – related submission documents, including preparation and review of project documentation for Health Authority submission, including briefing books, IBs, Annual Safety Reports, responses to Health Authority questions etc. Contributes to the ongoing clinical trial data medical/scientific review across assigned TCO studies and coordinates data analysis and interpretation Supports conduct of dose escalation meetings, investigator teleconferences and site initiation visits etc. Accountable for assigned close-out, roll-over and long-term follow-up studies, ensuring Clinical Study Report review, consistency and quality of clinical study reports (CSR) in collaboration with CSR medical writing team, and publication of studies across assigned TCO projects - either directly as lead author or by providing leadership to the medical writing team Maintains expert knowledge of ICH-GCP, external regulations and procedures, and supplements by training and practice of Novartis SOPs and internal policies. Advocate continuous improvement of quality Key performance indicators: Evidence of high-quality medical input to assigned studies to ensure execution according to timelines and ensuring adherence to international and local regulations. Evidence of quality medical and scientific review of clinical trial data Demonstrates excellent scientific writing skills to enable the development of high-quality documents including but not limited to clinical trial protocols, trial reporting (e.g. CSR), and regulatory documents (e.g. IB, DSUR). Contribution towards objectives set for the department. Feedback from external and internal stakeholders. Clearly demonstrates Novartis Values and Behaviors. Minimum Requirements: MD or equivalent medical degree required. Advanced knowledge and clinical training in a medical/scientific area (e.g., internal medicine / pharmacology etc.) with medical council certification required. Experience in hematology / oncology preferred. Work Experience: At least 2 years of pharmaceutical/biotech industry experience or at least 4 years of clinical practice experience in the hospital setting Knowledge of Good Clinical Practice (GCP). Strong operational project experience including excellent planning, prioritization, problem solving and organizational skills. Used to managing multiple priorities. Demonstrated operational excellence and scientific contribution to clinical or preclinical projects. Clear written and verbal expression of ideas, an active/proactive communicator. Well-developed interpersonal skills, with a proven record of accomplishment of successfully interacting with, influencing and building strong positive relationships. Used to working independently and in a team, being flexible and adapting in a changing environment. Skills: Clinical Monitoring. Clinical Research. Clinical Trial Protocol. Clinical Trials. Decision Making Skills. Drug Development. Health Sciences. Lifesciences. Regulatory Compliance. Languages : English. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards Division Biomedical Research Business Unit Pharma Research Location India Site Hyderabad (Office) Company / Legal Entity IN10 (FCRS = IN010) Novartis Healthcare Private Limited Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

MIT-World Peace University, Pune Job Title: Assistant Professor Department: Pharmaceutical Sciences School: Health Sciences and Technology Location: Pune Reports to: Program Director Position Summary MIT-WPU invites dynamic and committed academic professionals to apply for the position of Assistant Professor in the Department of Pharmaceutical Sciences , with specialization in: Pharmaceutical Chemistry Pharmacognosy Pharmaceutics Pharmacy Practice Pharmacology The ideal candidate will contribute to teaching, research, curriculum development, and student mentorship in alignment with MIT-WPU’s commitment to innovation, academic excellence, and societal impact. Eligibility Criteria Educational Qualifications: Graduation: B.Pharm Post-Graduation: M.Pharm Doctorate: Ph.D. in the relevant specialization Preferably from Top 50 NIRF-ranked institutions , IITs , or internationally recognized overseas universities Additional Desirables: UGC NET/SET/SLET qualified (preferred) Strong publication record in indexed journals Experience in curriculum development and innovative teaching methods Key Responsibilities Academic: Conduct lectures, tutorials, and practicals as per assigned workload Contribute to curriculum design and academic planning Participate in examinations, assessment, and academic audits Organize and participate in seminars, workshops, and faculty development programs Support soft skill development and industrial readiness of students Mentor and guide student projects and research Research & Development: Conduct high-quality research in specialization areas Publish in reputed national and international journals Assist in research grant writing and proposal development Promote student involvement in research and paper writing Strategic & Operational: Support the school’s academic and strategic initiatives Participate in student admission and outreach activities Supervise student development activities including study tours, internships, and immersion programs Provide academic and career mentoring to students Collaborations: Engage with industry partners for placements and projects Collaborate with academic bodies and participate in national academic events Contribute to the development of an active alumni and corporate network Personal Attributes Strong interpersonal and communication skills Passion for teaching and student development Commitment to MIT-WPU’s mission and values Open to interdisciplinary collaboration and innovation in pedagogy How to Apply 📩 Send your updated CV to: jidnyasa.jain.ve@mitwpu.edu.in About MIT-WPU MIT World Peace University is one of India’s leading private universities, committed to nurturing socially responsible leaders through a unique blend of academic excellence, research innovation, and value-based education. Show more Show less

OverviewCactus Life Sciences is a remote-first organization, and we embrace an accelerate from anywhere culture. You may be required to travel to our Mumbai office based on business requirements or for company/team events.If you are looking for challenging and rewarding work which combines your understanding of medical science and aptitude for writing into one unique job, the Senior Medical Writer role is for you. This is an opportunity to grow your career and make a greater impact on the lives around you. ResponsibilitiesTaking ownership and responsibility for development (write, review, proofread, and data-check) of high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client and audience needs with excellent attention to detail.Actively involve in reviewing materials developed by scientific writers to ensure strategic alignment and scientific accuracy as needed and providing clear constructive feedback, support, and supervision to writers. Mentor and train scientific writers by sharing best practices and client preferences, thereby contributing to skill development within the team.Having excellent knowledge of product/account to enable meaningful interactions with clients and authors, including consultancy where necessary.Building and maintaining strong, long-term relationships with international pharmaceutical clients, healthcare professionals, and key stakeholders, including authors, reviewers, and KOLs across therapeutic areas. This involves anticipating client needs, advising on strategic and tactical plans, and recommending improvements to scientific content and new ways to disseminate data effectively.Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives. Attending client and other external meetings and supporting senior team members as needed.Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans. Also, supporting with the development of visual content and materials using effective data visualization techniques and approaches. Contributing to innovative “out of the box” solutions for medical writing projects.You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and CACTUS’ internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date.Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines.Supporting with pitches, both during the preparation phase and the actual pitch. Qualifications And Prerequisites3-5 year of experience in relevant fields of scientific writing.PhD/MD (Pharmacology) OR PhD (Life Sciences) OR PharmD OR M.Pharm/M.Sc with a good understanding of clinical research and medical communication.Preferrable to have some experience working on Global Medical Value (GMV) Dossiers.Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills.Ability to adapt writing style to different materials and target audiences.Basic knowledge of biostatistics.Literature reviewing and evaluation capabilities.Very good working knowledge of MS Office. Application ProcessBefore applying, please ensure you meet the role requirements listed above and have legal authorization to work in the country where this role is advertised. Our selection process typically involves an initial screening by a recruiter, a technical assessment, and two to three interview rounds. For this role, the process starts with a Technical Interview with the Hiring Managers, followed by a Technical Assessment, where candidates will have agreed upon timeline to complete the task. The final round will be the HR Interview. All interactions will be conducted virtually via MS Teams. Equal OpportunityOur hiring practices reflect our commitment to providing equal opportunities and creating an environment where everyone can thrive, develop, and succeed. We celebrate the uniqueness of our team members and prohibit discrimination of any kind, based on race, color, religion, gender identity, sexual orientation, age, marital status, disability, or any other protected characteristic. Accelerating from AnywhereAs a remote-first organization, these are essential attributes we look for in all our candidates.Taking ownership of your work with minimal supervision, showing strong ability to organize, prioritize and deliver results independently.Documenting work that brings everyone on the same page.Maturity to choose between synchronous and asynchronous collaboration.Effectively collaborating with colleagues across different time zones by setting dedicated hours for collaboration and keeping team members updated through your MS Teams status. About CACTUSAt Cactus Life Sciences (cactuslifesciences.com), we believe the future of medical communications lies at the intersection of science, technology, and human connection. Headquartered in Princeton, New Jersey, with teams in Switzerland, the United Kingdom, India, and Japan, we help biopharmaceutical organizations redefine scientific exchange—leveraging AI, automation, and innovation while keeping patients at the heart of everything we do.Our expertise spans medical strategy, scientific content development, and medical education across therapeutic areas and the product lifecycle. By blending scientific rigor, agile operational models, and future-ready technologies, we partner with medical affairs teams to catalyze their transformation, adapt to a changing landscape, and drive meaningful outcomes for healthcare communities worldwide.

Job portal All vacancies 163925 Professor of Veterinary Biomedicine Professor of Veterinary Biomedicine Department of Veterinary and Animal Sciences Faculty of Health and Medical Sciences University of Copenhagen The University seeks to appoint a professor to the Department of Veterinary and Animal Sciences to commence 1 December 2025 or as soon as possible thereafter. Information on the department can be found at: https://www.sund.ku.dk/. Job Description When considering applications for the professorship, the main emphasis will be on the applicant's ability to document a high level of original scientific work at an international level within the area of Veterinary Biomedicine. The professorship is part of Section of Biomedicine that encompasses the topics of experimental and clinical pharmacology and toxicology, laboratory animal science and welfare, veterinary and nutritional immunology, comparative pediatrics and bioinformatics and are the main responsible for the biomedicine track on the veterinary education. Studying interactions between exposure and response in complex biological systems is a central part of the biomedicine track and thus research, supervision and teaching in this area will constitute the main focus of the professorship. This includes developing, validating and monitoring in vivo disease- and PK/PD models - for example for testing a novel drug in an experimental animal exhibiting a specific disease phenotype – and evaluating the pharmacokinetic (PK), pharmacodynamic (PD) and toxicological properties of a given compound. A successful candidate to the professorship must have substantial experience with these areas and across animal species. A broad and expanding field, Veterinary Biomedicine engages several disciplines. Besides pharmacology and toxicology, these include veterinary pathology, physiology and laboratory animal sciences. In addition, methods to analyze effects and endpoints are continuously emerging, encompassing areas within digital image analysis, histopathology, molecular biology and bioinformatics. A successful candidate must be able to document experience in at least some of these areas and show the ability to collaborate with colleagues from related disciplines. The professorship is required to develop and consolidate the field of Veterinary Biomedicine. This is expected to involve network activities through collaborations (e.g. with the biomedical industry), and through research-based education at pre- and postgraduate levels. Specifically, the professor will be responsible for the Biomedicine track for veterinary master students. Teaching activities include planning the course and curriculum, developing teaching materials, conducting practical and theoretical exercises and assessing students at the exam. Supervisor experience of bachelor, master and PhD projects, and supervision or mentorship of junior academic employees, is a requirement. Documented experience in research group management and leadership must also be included. The Professor’s Responsibilities Will Primarily Consist Of Research, including publication/academic dissemination and acquisition of external fundingResearch-based teaching, including associated examination, at all academic levelsResearch leadership, including guidance and supervision of researchersObligation to share knowledge with the rest of society, including participation in public debateAcademic assessments and active engagement in other administrative duties and committees within the Department and UCPH Required Qualifications To be qualified for a professor position, you will be assessed according to these six overall criteria for recognising merit at the University of Copenhagen: Research, teaching, societal impact, organisational contribution, external funding, and leadership. Find information about each criterion. Furthermore, Each Applicant Must Be Able To Document Document a high degree of original academic production at an international level, including considerable contributions to the development of the academic disciplineExtensive experience and formal training in leading a research groupExtensive experience to obtain and manage external funding for researchManage research and other management functions, e.g. engage in the university’s external academic activities, as well as knowledge and technology transferProvide research-based teaching including documentation of formal pedagogical qualifications and a record of pre and post graduate research-based teaching, preferable within the field of Veterinary Biomedicine The professor is also required to possess good interpersonal and communicative skills. Terms of employment The position is a permanent position. The average weekly working hours are 37 hours per week. Salary and other terms and conditions of appointment are set in accordance with the Agreement between the Ministry of Taxation and AC (Danish Confederation of Professional Associations) or other relevant professional organisations. The position is covered by the Job Structure for Academic Staff at Universities 2020. Questions For further information, please contact Head of Section, Professor Jens Lykkesfeldt (jopl@sund.ku.dk). Foreign applicants may find the university’s International Staff Mobility useful. Application The application must be submitted in English and must include the following documents: Application (Including motivation for applying for this position (Maximum 2 pages))Curriculum vitae (Including information about external funding)Diplomas (Master’s, PhD and other relevant certificates)A complete list of publicationsResearch plan (3‐5 pages)Uploads of maximum 10 publications to be considered in the assessmentTeaching planTeaching portfolio (Guidelines) Application procedure After the expiry of the deadline for applications, the authorized recruitment manager selects applicants for assessment on the advice of the Appointments Committee. All applicants are then immediately notified whether their application has been passed for assessment. The Dean then appoints an expert assessment committee in order to make an assessment of the selected applicants for the specific post. Selected applicants are notified of the composition of the committee and each applicant has the opportunity to comment on the part of the assessment that relates to the applicant him/herself. You can read about the recruitment process at the university's Job Portal. Please note that the applicant will be contacted if the assessment committee requires further documentation. The applicant will be assessed according to the Ministerial Order no. 242 of 13 March 2012 on the Appointment of Academic Staff at Universities. The University of Copenhagen encourages all interested applicants to apply for this position. Please submit the application with the required attachments. Only online applications will be accepted. The closing date for applications is 23.59 p.m. CET, 18 May 2025. Interviews for this position are likely to be held on 20 October 2025. APPLY NOW Part of the International Alliance of Research Universities (IARU), and among Europe’s top-ranking universities, the University of Copenhagen promotes research and teaching of the highest international standard. Rich in tradition and modern in outlook, the University gives students and staff the opportunity to cultivate their talent in an ambitious and informal environment. An effective organisation – with good working conditions and a collaborative work culture – creates the ideal framework for a successful academic career. Contact Jens Lykkesfeldt E-mail: jopl@sund.ku.dk Info Application deadline: 18-05-2025 Employment start: 01-12-2025 Working hours: Full time Department/Location: Department of Veterinary and Animal Sciences " id="cookiefilter-placeholder-1"> Content not available due to cookie preferences You cannot see the content of this field because of your cookie preferences. Click here to change your cookie settings. Category: Marketing Search all vacancies

*URGENT HIRING* *POST :- MBBS DOCTOR* *SALARY:- 1LAC TO 1.20 (PER MONTH)* *ACCOMMODATION AVAILABLE* *LOCATION:- CHAMPA CHHATTISGARH*

LOCATION Hyderabad, India DEPARTMENT Biology Please enter job description

Assistant Professor Specialties: Anatomy, Physiology, Pharmacology, Microbiology, Forensic Medicine, Anesthesia, and Cardiology Location: Jaipur About the Role: We are seeking passionate and knowledgeable Assistant Professors across multiple medical specialties to join our esteemed institution. The ideal candidates will bring academic excellence, a commitment to teaching and research, and the ability to mentor students effectively. Key Responsibilities: Deliver high-quality lectures and practical sessions. Guide and mentor students in their academic and professional development. Conduct and supervise research projects within the department. Engage in curriculum development to enhance learning outcomes. Collaborate with colleagues on interdisciplinary academic initiatives. Participate in institutional activities, committees, and faculty development programs. Qualifications & Skills: Minimum required qualifications: MD/MS/PhD or equivalent in the relevant specialty. Strong passion for teaching, research, and mentoring students . Prior experience in academic or clinical settings is preferred.

Fresher Hiring 2023 - 2025 Passouts only - All India Qualification - B.Pharm, M.Pharm, B.SC, M.SC, Life Sciences Graduates & Post Graduates Medical - BDS, BHMS, BAMS, MBBS Role & responsibilities Perform data reconciliation between different data sources and study documents to ensure data integrity and consistency across datasets. Generate data queries to address discrepancies, inconsistencies, and missing data identified during data review, ensuring timely resolution and documentation of data queries Communicate data queries to investigative sites, data managers, and study personnel, following up on query responses and resolving discrepancies in collaboration with relevant stakeholders Identify deviations from protocol-specified procedures, eligibility criteria, and data collection guidelines, escalating issues to appropriate personnel for resolution Perform quality checks and data validation procedures to ensure accuracy, consistency, and reliability of clinical trial data, adhering to data management standards and industry best practices Assist in the development and implementation of data validation plans, data review guidelines, and quality control procedures to maintain high standards of data quality and integrity. Assist in a variety of specialties including but not limited to primary care, orthopedics, rheumatology, etc. Updates patient history, physical exam, and other pertinent health information in the document as required. Complies with Compliance standards of the Organization as laid by HIPAA. Performs other duties and tasks to improve provider productivity and workflow as assigned by supervisors. Assist documenting the patients, electronic health record (EHR). Fresher Hiring - Pharma / Life Sciences / Medical Qualification - B.Pharm, M.Pharm, B.SC, M.SC, Life Sciences Graduates & Post Graduates Medical - BDS, BHMS, BAMS, MBBS Location - All India - Delhi, Mumbai, Pune, Bangalore, Kochi, Chennai, Hyderabad, Ahmedabad, Bhopal, Indore, Kolkata, Chandigarh

In this Role you will be Responsible for The coder reads the documentation to understand the patient's diagnoses assigned. Transforming of healthcare diagnosis, procedures, medical services, and equipment into universal medical alphanumeric codes Creating uniform vocabulary for describing the causes of injury, illness & death is the role of medical coders. Medical coding allows for Uniform documentation between medical facilities. The main task of a medical coders is to review clinical statements and assign standard Codes Requirements of the role include 1 Year of experience in any Healthcare BPO - University degree or equivalent that required 3+ years of formal studies in Life science/BPT/Pharm/Nursing Good knowledge in human Anatomy/Physiology Experience using a computer with Windows PC applications that required you to use a keyboard, navigate screens, and learn new software tools. Ability to work scheduled shifts from Monday-Friday 7:30 AM to 5:30 PM IST and the shift timings can be changed as per client requirements. Flexibility to accommodate overtime and work on weekend basis business requirements. Need to return to office when NTT Data provides communication related to that.During training you will be asked to work from office * Career Arch Job code Overview and General duties and tasks For Internal Reference Only

In this Role you will be Responsible For The coder reads the documentation to understand the patient's diagnoses assigned Transforming of healthcare diagnosis, procedures, medical services, and equipment into universal medical alphanumeric codes Creating uniform vocabulary for describing the causes of injury, illness & death is the role of medical coders Medical coding allows for Uniform documentation between medical facilities The main task of a medical coders is to review clinical statements and assign standard Codes Requirements of the role include 0 -1 Year of experience in any Healthcare BPO University degree or equivalent that required 3+ years of formal studies in Life science/BPT/Pharm/Nursing Good knowledge in human Anatomy/Physiology 1+ year(s) of experience using a computer with Windows PC applications that required you to use a keyboard, navigate screens, and learn new software tools Ability to work scheduled shifts from Monday-Friday 7:30 AM to 5:30 PM IST and the shift timings can be changed as per client requirements. Flexibility to accommodate overtime and work on weekend’s basis business requirement. Ability to communicate (oral/written) effectively in English to exchange information with our client