169 Drug Jobs - Page 5

You'll be crucial in ensuring clients receive quality data by meticulously reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations . Essential Duties and Responsibilities Apply GMP/GLP in all areas of responsibility, as appropriate. Demonstrate and promote the company vision. Ensure regular attendance and punctuality. Read and understand analytical procedures. Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs. Gain a technical understanding of the techniques for which review is being performed. Use MS Windows applications such as Excel, Word, Access, and Outlook email. Conduct all activities in a safe and efficient manner. Perform other duties as assigned. Qualifications Education/Experience: Master's degree in a science-related field (Biochemistry / Biotechnology / Microbiology) with 3-7 years of experience in Bio/Pharmaceutical drug product/substance testing with knowledge of regulatory requirements. Experience with analytical techniques such as qPCR, microbiological techniques, knowledge of USP/EP/JP compendia , and laboratory software applications such as PCR analysis software, bioinformatics tools, and LIMS is preferred. Key Candidate Attributes Self-motivation ; excellent quality of work and attention to detail. Ability to communicate effectively with coworkers and internal/external clients. Ability to learn new tasks quickly and to move easily from task to task. Ability to handle prioritization and multiple tasks simultaneously . Ability to use a personal computer and learn necessary programs. Good communication skills (oral and written). Organizational ability and good judgment. Science background/education and/or laboratory experience. Strong Math Skills. Logical Thinking, Good Reasoning Ability. Motivation to excel. Coaching/mentoring of peers.

Eurofins Scientific is an international life sciences company that provides a wide range of analytical testing services to clients across multiple industries. From food and pharmaceuticals to environmental and cosmetic products, Eurofins ensures safety, authenticity, and accuracy. With a global presence and over 900 laboratories, Eurofins is a leader in food, environmental, pharmaceutical and cosmetic product testing, as well as in genomics, clinical studies support, and other specialized diagnostic testing. Position Summary: Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations Essential Duties and Responsibilities: Exercise discretion and independent judgment with respect to matters of significance directly related to the management or general business operations through the data review process Perform review of scientific data, including, but not limited to standard preparation, calibrations, methodology, QC, sample data, compound evaluation and other subjective review based on testing performed; perform complex calculations to verify results Verify the data is of sound quality and determine if data is compliant and defendable based on industry regulations and methodology May serve as technical advisor for analysts with regard to QA/QC of data Diagnose problems; solve simple problems, and suggest solution to complete problems in professional area Keep oneself and peers abreast of current developments and trends in professional area by reading and understanding internal procedures, attending/providing training sessions, by writing/revising SOPs (as required), and by assisting Group Leader / Principal Specialists in training new and existing employees Use MS Windows applications such as Excel, Word, Access, Outlook email; create complex Excel worksheets and formulas Communicate with internal clients to discuss any findings and notify them of any necessary rework or compliance/regulatory concerns Conducts all activities in a safe and efficient manner Attention to details Works in collaboration Performs other duties as assigned Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrate and promote the company vision Regular attendance and punctuality Read and understand analytical procedures Qualifications Education/Experience (BMQ: Masters degree in a science-related field with 6-10 years of experience in Bio/Pharmaceutical Chemistry drug product/substance testing with knowledge of regulatory requirements. Theoretical / Practical experience with analytical techniques such as Ligand binding assays, ELISA, Gel electrophoresis, Proteomics, Flow Cytometry, TEM, PCR, cell culture and cell-based assays (such as reporter gene, cell signaling, and cell proliferation). etc. Knowledge of USP/EP compendia, and laboratory software applications such as LIMS, Electronic Notebook is preferred. Additional Information Key Candidate Attributes: Self-motivation; excellent quality of work and attention to detail Ability to communicate effectively with coworkers and internal/external clients Ability to learn new tasks quickly and to move easily from task to task Ability to handle prioritization and multiple tasks simultaneously Ability to use a personal computer and learn necessary programs Good communication skills (oral and written) Organizational ability and good judgement Science background/education and/or laboratory experience Strong Math Skills Logical Thinking, Good Reasoning Ability Motivation to excel Coaching/mentoring of peers

Responsibilities: Dispense medications accurately and safely to patients, ensuring proper labeling and instructions. Counsel patients on medication use, potential side effects, and interactions. Monitor patient profiles for potential medication errors or allergic reactions. Collaborate with healthcare professionals to optimize patient care. Maintain inventory, manage stock levels, and ensure proper storage of medications. Adhere to pharmacy laws, regulations, and hospital policies. Participate in quality improvement initiatives. Respond to patient queries and concerns. Maintain patient confidentiality and uphold professional standards. Desired profile of the candidate: Diploma in Pharmacy (D.Pharm) Bachelor's degree in Pharmacy (B.Pharm) Registration with the relevant pharmacy council Strong communication and interpersonal skills Attention to detail and organizational skills Ability to work in a fast-paced environment

We're Hiring! Join Tata 1mg, India's leading digital healthcare platform, and be a part of our growing team in Delhi. We're looking for passionate and skilled individuals for the following roles: Pharmacist & Senior Pharmacist Location: Delhi Employment Type: Full-Time | On-Site Qualification: Diploma in Pharmacy (D.Pharm), Bachelors (B.Pharm), or Masters in Pharmacy (M.Pharm) Key Responsibilities: Dispense prescribed medicines accurately with correct dosage and labelling. Provide drug information and counseling to customers/patients. Maintain records of prescriptions, invoices, and inventory. Ensure compliance with pharmacy regulations and SOPs. Supervise junior staff (for senior roles) and assist in store operations. Monitor expiry dates and manage returns and damages. Eligibility Criteria: D.Pharm / B.Pharm / M.Pharm from a recognized institute. Minimum 1 years of experience preferred (Senior Pharmacist: 3+ years). Registered with State Pharmacy Council. Strong knowledge of medications, brand-generic mapping, and patient care. Good communication and customer-handling skills. Prior experience in a retail pharmacy or healthcare company is a plus. Why Join Tata 1mg? Work with one of the most trusted names in healthcare. Opportunity for career growth and internal promotions. Access to training, wellness, and employee development programs. Competitive salary + performance-based incentives. Role: Healthcare & Life Sciences - OtherIndustry Type: Medical Services / HospitalDepartment: Healthcare & Life SciencesEmployment Type: Full Time, PermanentRole Category: Healthcare & Life Sciences - OtherEducationUG: B.Pharma in Any SpecializationPG: M.Pharma in Any Specialization Role: Pharmaceutical & Biotechnology - OtherIndustry Type: Pharmaceutical & Life SciencesDepartment: Research & DevelopmentEmployment Type: Full Time, PermanentRole Category: Pharmaceutical & BiotechnologyEducationUG: B.Pharma in Any SpecializationPG: M.Pharma in Pharmacy Role: Healthcare & Life Sciences - OtherIndustry Type: Pharmaceutical & Life SciencesDepartment: Healthcare & Life SciencesEmployment Type: Full Time, PermanentRole Category: Healthcare & Life Sciences - OtherEducationUG: B.Pharma in PharmacyPG: M.Pharma in Pharmacy

Responsibilities: Dispense medications accurately and efficiently Collaborate with healthcare team on patient care plans Ensure compliance with regulatory standards Manage inventory and order supplies

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Job Purpose: Provide medical review, analysis and guidance during the case handling and reporting cycle of Adverse Event and Adverse Reaction reports received for investigational and marketed products Provide medical guidance and input to Drug Safety Associates (DSAs) and specialists in medical aspects of drug safety Function as pharmacovigilance representative/safety scientist General Maintaining a good working knowledge of the Adverse event profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and international drug safety regulations Maintaining an awareness of global regulatory requirements and reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting Maintaining excellent knowledge of the safety profile of assigned products Communicating and discussing issues related to review process with Project Manager Interacting with internal and external contacts for resolving issues Maintaining a good working knowledge of relevant regulatory guidelines Attend and present client/cross functional meetings along with other stakeholders Training and mentoring new team member, as required Working as Subject Matter Experts (SMEs) Assisting the Manager for inspection readiness activities and audits Provides inputs for process improvisations Works closely with Manger for process co-ordination and to ensure meeting all KPIs for the process. Case report Medical review (as applicable) Performing medical review of cases according to client Standard Operating Procedures (SOPs) and liaising with the client, as required Writing Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assessing company causality Assessing seriousness and expectedness of reported events Providing medical advice to DSPs and case processing team Skills: Excellent interpersonal, verbal and written communication skills Computer proficiency, an ability to work with web-based applications and familiarity with the Windows operating system Client focused approach to work A flexible attitude with respect to work assignments and new learnings Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail Ability to assess the clinical relevance of medical data and to interpret its clinical meaning is essential Willingness to work in a matrix environment and to value the importance of teamwork Strong knowledge of international drug regulation including GCP, GVP Knowledge and Experience: Relevant experience of minimum 2 Years in Pharmacovigilance/ drug safety is desirable. Education: MBBS/Post Graduation in Medicine.

We are seeking a licensed and detail-oriented Pharmacists to join our team. Candidate will be responsible for dispensing prescriptions, providing medication counseling, ensuring regulatory compliance, and supporting overall patient health outcomes. Required Candidate profile Interested Candidates Drop CVs to HR Priyanshu WhatsApp: +91 99882-18886 Mail: recruitment@amandeephospital.org

Join Our Team at Alliance Pharmacy! Now Hiring: Pharmacist & Pharmacist Assistant Are you passionate about healthcare and community service? Alliance Pharmacy is looking for dedicated and skilled professionals to join our growing team! If you're seeking a dynamic and rewarding work environment where you can make a real difference in people's lives, this is the opportunity for you. Why Join Us? Work in a professional and supportive setting. Contribute meaningfully to community health. Opportunities for career growth and development. Be part of a respected and expanding healthcare brand Positions Available: Pharmacist Pharmacist Assistant Job description Accommodation Provided by the Company Only for Male Candidates. Key Responsibilities: Compounding and dispensing medications, as prescribed by physicians. Suggest over-the-counter medicines for common ailments. Provide alternate options when prescribed brands are unavailable. Ensure accurate medication dispensation and customer satisfaction. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Advise customers on general healthcare. Check the stock against the invoices, for quantity, batch no, expiry etc. Stocktaking of short-expiry medicines in regular intervals. Taking the stock of non-moving medicines once in regular intervals. Doing physical verification of stocks with computer data in regular intervals. Check the Inventory of the desired Pharmacy once in a month. Perform invoicing and billing tasks with basic computer skills. Maintaining registers & records as required under the applicable laws. Skills Required: In-depth knowledge of medicines and pharmaceutical products. Strong commitment to serving the community and ensuring customer well-being. Good interpersonal skills and a customer-first attitude. Basic computer proficiency. For Pharmacists: D. Pharm / B. Pharm / M. Pharm (Freshers / Experienced) For Assistants: Minimum 12th Pass / Any Graduate (Freshers / Experienced) Take the next step in your career with Alliance Pharmacy, where care meets commitment. Apply now and be a part of something meaningful! WhatsApp or Email the given below. Thanks & Regards, HR Department WhatsApp: 74032 56789 Email: hr@alliancepharmacy.in

Roles and Responsibilities : The purpose is to dispense medicines prescribed by doctors and other health professionals and provide information to patients about medications and their use. Qualification: Bachelors in Pharmacy / Diploma in Pharmacy Experience: 1 to 5 Years Registration in Karnataka Pharmacy Council in mandatory* Review prescriptions from doctors to ensure accuracy, to ascertain the needed ingredients, and to evaluate their suitability for the patient Assist in advising patients regarding drug dosage as required Stock managing and check for expiry date every month, maintain adequate stock levels Assist in ordering and receive medicines from pharmacy stores Ensure proper handling and storage of drugs in pharmacy Ensure all the activities in the pharmacy bulk store are carried out as per protocol Skills & Knowledge: Pharmacology and Pharmacy system knowledge Analysing information and administering medication Health regulations and legal compliance Working knowledge of SOP, Quality and NABH Standards Basic Computer Operations Please write "Application for the post of Hospital Pharmacist" in Subject column while sending an E-mail. Pharmacist: 1 year (Required) License/Certification: • Karnataka Pharmacy Council (Required) Desired Candidate Profile Able to work accurately and with minimal supervision. Compound and dispense medications as prescribed by doctors, by calculating, weighing, measuring, and mixing ingredients, or oversee these activities. Ability to comprehend written instructions given by the Doctors and the other related departmental personnel. Ability to plan & organize ones work schedule effectively. Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel. Affinity to work in team Enthusiasm. Open mindedness. Experience - 0-3 Yrs Perks and Benefits As per company standards

Roles and Responsibilities Provide clinical pharmacy services to patients, including dispensing medications and counseling on their use. Authorize prescriptions and monitor patient treatment plans in collaboration with healthcare providers. Participate in quality improvement initiatives to enhance patient care and satisfaction. Desired Candidate Profile 1-5 years of experience as a Clinical Pharmacist or related field (pharmacy, biotechnology). Strong knowledge of pharmacy operations, drug authorization processes, and regulatory requirements. Excellent communication skills for effective interaction with patients, families, and healthcare professionals. Ability to work independently while prioritizing tasks effectively under pressure.

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Job Purpose: Provide medical review, analysis and guidance during the case handling and reporting cycle of Adverse Event and Adverse Reaction reports received for investigational and marketed products Signal detection/analysis/evaluation and ongoing safety surveillance activities Provide medical guidance and input to Drug Safety associates (DSAs) and specialists in medical aspects of drug safety Function as pharmacovigilance representative/safety scientist General Maintaining a good working knowledge of the Adverse event profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and international drug safety regulations Maintaining an awareness of global regulatory requirements and reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting Maintaining excellent knowledge of the safety profile of assigned products Communicating and discussing issues related to review process with Project Manager Interacting with internal and external contacts for resolving issues Maintaining a good working knowledge of relevant regulatory guidelines Attend and present client/cross functional meetings along with other stakeholders Case report Medical review Performing medical review of cases according to client Standard Operating Procedures (SOPs) and liaising with the client, as required Writing Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assessing company causality Assessing seriousness and expectedness of reported events Providing medical advice to case processing team Skills: Excellent interpersonal, verbal and written communication skills Computer proficiency, an ability to work with web-based applications and familiarity with the Windows operating system Client focused approach to work A flexible attitude with respect to work assignments and new learnings Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail Ability to assess the clinical relevance of medical data and to interpret its clinical meaning is essential Willingness to work in a matrix environment and to value the importance of teamwork Strong knowledge of international drug regulation including GCP, GVP Knowledge and Experience : Good knowledge of medical terminology. Fresher/ relevant experience into pharmacovigilance/ Drug Safety field is preferred. Education: MBBS/MD

A Hospital Pharmacist is Responsible for dispensing medications, ensuring their safety and efficacy, and providing drug information to patients and healthcare professionals. Responsibilities: Maintain stock, supplies, and inventories of all medicines. Will be responsible for the preparation of indents for the hospital Pharmacy. You will maintain the Stock Registers. Will be responsible for checking the expiry dates of drugs/medicines and arranging timely consumption or replacement thereof. Maintains a checklist and takes inventory of high alert medications/narcotics/backup pharmacy on a daily basis. The Pharmacist is responsible for monitoring the supply of all medicines used in the hospital Will be responsible for any other duties assigned by the Reporting Manager from time to time. May also be involved in drug safety monitoring and quality improvement initiatives. Skill Sets: Verbal Ability/Communication Skill Problem Solving/Decision Making Leadership Qualities Education: D Pharm OR B Pharm Freshers can also apply for this job. There is an opening for full-time as well as Part-time pharmacist.

Title Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Data Coder to join our Clinical Coding & Support team in Mumbai, India. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous coding, pharmacy, or nursing expertise and can develop and grow your career even further, then this is the opportunity for you! Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Responsibilities Perform accurate coding of medical terms and medications utilizing industry-wide standards as well as company standards; Coordinate the assignment of appropriate dictionaries for meeting study requirements; and Develop and maintain coding guidelines Qualifications Bachelor Degree in Nursing, or more advanced clinical degree; Experience with using MedDRA and WHO Drug dictionaries; and Experience working with clinical trials or within the pharmaceutical environment is preferred. People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Title Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Data Review Associate in Mumbai, India to join our Global Clinical Coding & Support team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous nursing expertise and can develop and grow your career even further, then this is the opportunity for you! Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. Responsibilities Comprehensive manual review of clinical data collected in trials Development of clinical review guidelines for specific therapeutic areas Interface with Data Management team to assure query resolution Seeking specialization in following therapeutic areas: Oncology Hematology Infectious Disease Endocrinology Metabolic disorders Qualifications Bachelor’s Degree in Nursing / Medicine, or more advanced clinical degree Professional / or Post-Qualification Nursing experience, preferably in Oncology and Hematology background General knowledge of clinical trial processes and/or experience working with clinical data Experience with using MedDRA and WHO Drug dictionaries will be a plus. People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. Medpace Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What to Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Job Title: Pharmacist Company Name: Manipal Hospitals Job Description: Manipal Hospitals is seeking a dedicated and knowledgeable Pharmacist to join our healthcare team. The ideal candidate will be responsible for ensuring the safe and effective use of medications for our patients. Roles and Responsibilities Roles and Responsibilities: 1. Dispense medications and ensure the accuracy of prescriptions provided by healthcare professionals. 2. Counsel patients on the proper use of medications, potential side effects, and drug interactions. 3. Collaborate with doctors, nurses, and other healthcare staff to optimize patient care and medication management. 4. Conduct medication reviews and maintain patient medication profiles to ensure safe and effective therapy. 5. Monitor and manage the inventory of pharmaceuticals, ensuring adequate stock levels and proper storage conditions. 6. Provide drug information and education to both patients and healthcare professionals. 7. Participate in quality improvement initiatives and adhere to regulatory standards and hospital policies. 8. Maintain accurate and detailed records of all pharmacy activities, including prescriptions dispensed and medication errors. 9. Supervise pharmacy technicians and support staff in their daily tasks and responsibilities. 10. Stay updated on new medications and treatment protocols, continuing professional development. Qualifications: - Bachelor's degree in Pharmacy or Pharm.D. from an accredited institution. - Valid pharmacist license in the respective state. - Strong knowledge of pharmacology and pharmaceutical care practices

1. Clinical Trial Design and Oversight, 2. Drug Efficacy and Safety Analysis, 3. Drug Interactions and Adverse Reactions, 4. Research and Development, 5. Compliance and Regulatory Affairs, 6. Patient Counseling, 7. Monitoring Drug

Interested candidates can come for the direct walk-in on dated 06-06-2025 (Friday) to 10-06-2025 (Tuesday) Timing: 10:00 AM JOB SPECIFICATION: Educational Qualification: Diploma/B Pharmacy Experience 0 to 6 Years PCI License Mandatory

Life-changing careers - Check out this open position at Novo Nordisk Job description Job description Are you an experienced medical professional and passionate about Clinical MedicalDoes being part of a growing, yet dynamic environment excite youIf yes, then you may be the one we are looking for as Clinical Medical Manager for Novo Nordisk India. Apply now! As a Clinical Medical Manager, you will be responsible for : Facilitate the execution of clinical trials related to New Therapy Areas (including CVD, CKD, NASH) by providing medical/scientific expertise and advice. Identify and map KOLs, investigators, and research center s within the relevant therapy areas. Collect early scientific insights and guidance by discussing relevant early development data with external medical and scientific experts. Contribute to delivering successful clinical trials (phase I-IV) in collaboration with clinical operations. Provide timely medical guidance and internal training to clinical staff. Engage in extensive scientific communication both internally and externally, requiring strong presentation skills. Performing ad hoc visits, Supporting attendance at investigator meetings, ensuring KOL inclusion in clinical trials and engaging key investigators to communicate trial results. Qualifications To be successful in this role, you should have the following qualifications: MD in any discipline with a strong clinical research/medical affairs background. 5 years of clinical or pharmaceutical industry experience with strong experience in human healthcare research either from university, CROs, or pharmaceutical industry. Expertise in therapeutic areas of relevance (CVD, CKD, NASH), preferably with authorship in peer-reviewed journals. Understanding of pharmaceutical drug development. Open to domestic and international travel in connection with site visits, congresses, and company events. Experience as a clinical trial investigator or sub-investigator. Understanding the specificities and nuances of the local healthcare infrastructure. The CMR (Clinical, Medical, Regulatory & Pharmacovigilance) team based in Bangalore. Our team is dedicated to driving clinical trials and providing medical/scientific expertise in New Therapy Areas. We work closely with KOLs, independent professional associations, and patient advocacy associations to ensure the successful execution of clinical trials. The atmosphere is collaborative and dynamic, with a strong focus on scientific excellence and patient outcomes. Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 72,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we re working toward something bigger than ourselves, and it s a collective effort. Join us! Together, we go further. Together, we re life changing. To submit your application, please upload your CV and motivational letter online (click on Apply and follow the instructions). Internal candidates are kindly requested to inform their line Managers before applying. It has been brought to our attention that there have recently been instances of fraudulent job offers, purporting to be from Novo Nordisk and/or its affiliate companies. The individuals or organizations sending these false employment offers may pose as a Novo Nordisk recruiter or representative and request personal information, purchasing of equipment or funds to further the recruitment process or offer paid trainings. Be advised that Novo Nordisk does not extend unsolicited employment offers. Furthermore, Novo Nordisk does not charge prospective employees with fees or make requests for funding as a part of the recruitment process. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we re life changing.

Job description Bangalore, India Job category Clinical Development Department Centralised Monitoring Unit (CMU) Does your motivation come from challenges and working in a dynamic environmentDo you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essentialDo you have a can-do attitude with continuous improvement as one of your career objectivesThen we might have the right position for you. Apply now and join a growing team, working in an international environment. About the department The Centralised Monitoring Unit (CMU)- Bangalore, is a department within the Clinical Drug Development area. It is a perfect blend of skilled medical professionals (Medical reviewers) and technical programmers (Functional programmers, statistical monitors). Medical reviewers are actively involved in Risk-based medical monitoring in collaboration with the medical specialists from Denmark, with a focus on ensuring overall patient safety and wellbeing of all clinical trial participants, by ensuring compliance to protocol and identifying potential clinically significant outliers that require medical attention and medical data cleaning. The Functional Programmers develop operational visualizations in data visualization tools to support the trial teams on proactive centralized monitoring and Statistical Monitors perform the detection of unusual data patterns, systematic errors, and potential lack of compliance or fraud across trials. The Position (NoteThis is not a role within Pharmacovigilance) The Key Responsibilities in this position will be to perform a Medical Review of all trial subjects of all assigned clinical trials within the drug development portfolio across therapy areas & to ensure high-quality quality consistent medical data. Medical Review is performed for all trial subjects to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, local regulations, and Standard Operating Procedures (SOPs). Senior Medical Reviewer ensures high-quality medical data through medical review of clinical trial data. Ensure close collaboration with relevant study group members, especially the Data Manager, Trial Manager(s), and Medical Specialists during trial conduct. Report the status of the medical review to the project as appropriate, following the project communication plan and blinding plan. Consult with Trial Managers and Medical Specialists as appropriate to ensure medical review issues are escalated in a timely manner. Responsible for contribution to or participation in trial planning activities related to medical review. Perform the quality check measure for the medical review. Responsible for clarifying and if possible, resolving issues of medical concern and inconsistencies in clinical trial data with staff at investigational sites. Responsible for presenting findings of Medical Review to relevant Medical Specialists to enable decision-making. Responsible for documenting medical reviews in the sponsor TMF. Ensure close collaboration with relevant study group members, especially the Data Manager, Trial Manager(s), and Medical Specialist during trial conduct. Provide training on the project and process to the new team members. Review and provide inputs to MMP as well as Medical Monitoring, Displays or other data listing required to perform Medical review. The input should ensure unambiguous monitoring requirements as well as medical monitoring displays and data listing to enable efficient medical review. Qualifications Minimum as Graduate in Medicine or other relevant (MBBS & MD in pharmacology preferred, MBBS & MD in other clinical/paraclinical areas with relevant experience in clinical patient management/ clinical research). 2-3 years of experience as a Medical Reviewer is preferred. 1-2 years of experience in project management is required. Good knowledge of ICH (International Council for Harmonisation of Technical for Pharmaceuticals for Human Use), and GCP (Good Clinical Practice). Demonstrated computer skills (MS Office, MS Project, PowerPoint). Excellent understanding of medical terminology and clinical trial activities. Strong Analytical skills and result-oriented. Excellent written and spoken English. Working at Novo Nordisk Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we re working toward something bigger than ourselves, and it s a collective effort. Join us! Together, we go further. Together, we re life-changing. Contact To submit your application, please upload your CV online (click on Apply and follow the instructions). 10th May 2024. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we re life changing. Print job Send to e-mail Related jobs

Job Title: Pharmacist OPD Clinic Location: Bangalore Experience: Fresher to 6 years Qualification: D.Pharmacy / B.Pharmacy / M.Pharmacy Certificate: KSPC Registration is mandatory Job Description: Dispense medicines as per doctor’s prescription Explain dosage and usage to patients Maintain medicine stock and expiry records Coordinate with doctors and staff for smooth pharmacy operations Handle billing and basic pharmacy software Key Skills: Pharmacist, OPD, Dispensing, KSPC, Patient Counselling, Inventory Job Type: Full-time (Rotational shift if required)

Qualifications & Experience: Position Qualification & Experience Pharmacist Grade IV - D.Pharm / B.Pharm with 2 years of post-qualification experience Pharmacist Grade III - D.Pharm / B.Pharm with 4 years of post-qualification experience Pharmacist Grade II - D.Pharm / B.Pharm with 6 years of post-qualification experience Pharmacist Grade I - D.Pharm / B.Pharm with 8 years of post-qualification experience Assistant Pharmacist - D.Pharm /B.Pharm Date of Walk-In Selection - Venue of Walk-In Selection 09.06.2025 : HLL Management Academy, Keston Road, Near Style Plus, Kowdiar, Thiruvananthapuram-695003 09.06.2025 : GINGER, NH - 544, Near CUSAT Metro station, South Kalamassery, Kochi- 682033 10.06.2025 : Zip By Spree Hotels Mangala Towers, Paliyam Rd, Near North Bus stand, Patturaikkal, Thrissur-680001 11.06.2025 : HLL Pharmacy & Surgicals, Govt District Hospital Kannur -670017 12.06.2025 : Oshin Hotels, Opp. Civil Station, Kalpetta, Wayanad, Kerala - 673 122 13.06.2025 : HLL Pharmacy & Surgicals, Ground Floor, Super Speciality Block, Govt. Medical College, Kozhikode - 673008 Reporting Time: 10 am to 1 pm Selection procedure: The selection process for the positions of Pharmacist (Grade IV to I), and Assistant Pharmacist comprises of written test and interview. The written test for all the posts shall comprise of multiple-choice questions which should be answered in 30 minutes time and the maximum mark for the written examination is 50. There are no negative marks for wrong answers. Age: The maximum age limit for applying to the above positions is 37 years as of 01.06.2025 General Conditions: Before applying, candidates should ensure that they fulfil all the eligibility criteria mentioned in the advertisement. Only Indian Nationals are eligible to apply. SC/ST/OBC/PwD candidates will be eligible for relaxation as per Government of India directives. The crucial date for determining the age limit shall be same as the cut of date for calculating Qualification & Post Qualification Experience of the candidates. HLL reserves the right to cancel, restrict, or modify the selection process, or to not fill any or all of the posts notified, at its discretion. The number of vacancies may also be increased or decreased based on organizational requirements. The decision of Management regarding selection will be final. Canvassing in any form will be a disqualification. Candidates are required to bring all their original certificates along with self-attested copies to prove age, qualification, mark sheets, experience certificates, latest salary certificate with break-up, Aadhaar, PAN, and recent passport-size photographs for verification. SC/ST/OBC (Non-Creamy Layer) candidates must produce their community certificate in original issued by the concerned Revenue Authorities. Failure to produce the original certificates will result in disqualification from the selection test The appointment will be on a Fixed Tenure Contract basis. The proposed place of posting shown in detail may vary as per the business requirement, management keeps the right for the final place of posting as deemed fit. Only candidates with relevant QUALIFICATION and EXPERIENCE will be permitted to attend the written test. Candidates applying for the post of Pharmacist (Grade IV to I) / Assistant Pharmacist must submit their State Pharmacy Council Registration Certificate in order to obtain the pharmacy license for the outlet. For further clarification contact: 9188401559 or email to rbdhr@lifecarehll.com Page 1 of 2

Hiring For Retail Pharmacist Designation: Healthcare Executive and Senior Healthcare Executive(LICENSE IS MANDATORY ) Role: Retail - Pharmacist Department: B&M Retail Salary- upto 3 LPA Employment Type: Full Time, Permanent Role Category: Pharmaceutical & Biotechnology Education UG: B.Pharma in Pharmacy What will you do: Dispensing of Medication as per the prescription given by the Doctor. Inventory management as per the requirement of the market. Check for compliance related to patient confidentiality & scheduled drugs and maintain thorough documentation Must be communicating as tactfully as per the need of a business. What we are looking for: Bachelors degree or Diploma in Pharmacy or related field. Free Registration from State Pharmacy Council . Strong customer service and communication skills. Ability to multitask and good analytical skills. Proficiency with computers and software applications. Concern person : rubina.a@1mg.com \ 8860341813

Present suitable promoted products Liaise with and persuade targeted doctors to prescribe our products utilizing effective selling skills and performing cost-benefit analysis Provide product information and deliver product samples Required Candidate profile Familiarity with databases, statistics, product lines and latest medical issues Negotiation and sales skills Highly motivated and target driven with a proven track record in sales Perks and benefits Health insurance Retirement plans Paid time off

Review and execute physician’s prescriptions checking their appropriateness and legality. Maintain full control over delivering, stocking and labeling medicine and other products and monitor their condition to prevent expiring or deterioration. Required Candidate profile Thorough understanding of dosage administration and measurement, chemical compounds, medical brands etc. Excellent communication skills with a customer oriented approach. Integrity and compassion. Perks and benefits Health insurance Retirement plans Paid time off

Join a fast-growing cancer therapy company that's making a real impact in the fight against cancer. We're looking for a dynamic National Sales Manager to lead our pan-India sales strategy and drive growth in our oncology portfolio. Call 8169631633 Required Candidate profile Must have 15-20+ years of experience in oncology in highend drugs or BMT