2866 Pharmacology Jobs - Page 41

Company Description Established in 2013, GD Goenka University is a premier multidisciplinary institution located in Gurugram, Delhi NCR. With a vision to empower the next generation of thought leaders, the university offers undergraduate, postgraduate, and doctoral programs that equip students with skills and knowledge for a global economy. Recognized by prestigious organizations such as UGC, BCI, and ICAR, the university is committed to academic rigor, research and innovation, and holistic development. It operates 8 schools and hosts a diverse body of over 5,000 students and 11,000 alumni from over 45 countries. The 60-acre sustainable campus includes state-of-the-art facilities, including ...

Project Role : Engineering Services Practitioner Project Role Description : Assist with end-to-end engineering services to develop technical engineering solutions to solve problems and achieve business objectives. Solve engineering problems and achieve business objectives using scientific, socio-economic, technical knowledge and practical experience. Work across structural and stress design, qualification, configuration and technical management. Must have skills : 3D Modeling Good to have skills : NA Minimum 2 year(s) of experience is required Educational Qualification : BE or BTech Summary: As an Engineering Services Practitioner, you will be responsible for providing end-to-end engineering...

ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS Feasibility Grid Preparation: Preparing the feasibility for the Clinical trials as per the requirement of the sponsors. Reviewing Feasibility Questionnaires and feasibility reports. Medical Writing: Prepare and review study related docum...

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 p...

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 p...

Work Location - Alwarpet, Chennai Job Responsibilities :- Roles and Responsibilities - Pharmacy operations management Team leadership and management Patient counseling and education Pharmacology and pharmacokinetics Pharmaceutical calculations Diploma in Pharmacy Company will provide accomodation to stay with fixed salary . Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹20,000.00 per month Location: Chennai, Tamil Nadu (Required) Work Location: In person

Job Title: Sr. Regulatory Executive Location: Vadsar, Gandhinagar CTC: ₹4.0 LPA – ₹6 LPA Experience Required: 2–4 years in Regulatory Affairs (Pharma or Cosmetics) Educational Qualification: B.Pharm / M.Pharm – Drug Regulatory Affairs, Quality Assurance, Pharmacology, or Pharmaceutical Analysis Roles & Responsibilities: Prepare and review dossiers in accordance with regulatory guidelines (EU, GCC, USFDA, and other markets). Review, verify, and approve artworks, labels, and packaging components to ensure compliance with regulations. Prepare and maintain regulatory documents , technical files, and submissions for product approvals and renewals. Coordinate with internal departments (R&D, QA, QC...

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us Your Role Lead Medical Affairs activities in the assigned territory, ensuring scientific integrity, collaboration with Key Opinion Leaders (KOLs), and alignment with both global and local medica...

The Position Will be responsible for executing medical affairs strategy in the assigned zone. Tasks & Responsibilities Understand the current practices, medicines being used, and trends in relation to their respective therapeutic area through key customer contacts, attending scientific symposia and reviewing key therapeutic journals in order to provide relevant information to internal and external customers. Effectively gathers and disseminates information in a concise and understandable format to both internal and external customers and position BI Medical as a preferred partner for key customers through credible and clear non-promotional communication Execute key medical projects (e.g. IIS...

The Position Will be responsible for executing medical affairs strategy in the assigned zone. Tasks & Responsibilities Understand the current practices, medicines being used, and trends in relation to their respective therapeutic area through key customer contacts, attending scientific symposia and reviewing key therapeutic journals in order to provide relevant information to internal and external customers. Effectively gathers and disseminates information in a concise and understandable format to both internal and external customers and position BI Medical as a preferred partner for key customers through credible and clear non-promotional communication Execute key medical projects (e.g. IIS...

Need Fresh graduate with Strong understanding of Human anatomy and physiology, Proficiency in medical terminology and ability to learn new terms quickly. Takehome salary - 15.2 K per month (After all deduction) + Yearly Bonus Work Location - Ambattur IE / Ramapuram No direct walk -in only shortlisted will be called for interview, Whatsapp - 7825855974 (No calls only whatsapp message) for details We intend to hire 300 new medical coders each month. We recommend you to either enroll in a medical coding training institute or improve your knowledge in human anatomy and physiology on your own to be prepared for this opportunity. Please contact me once you are ready

Need Fresh graduate (Pharmacist) Strong understanding of Human anatomy and physiology, Proficiency in medical terminology and ability to learn new terms quickly. Takehome salary - 15.2 K per month (After all deduction) + Yearly Bonus Work Location - Ambattur IE / Ramapuram No direct walk -in only shortlisted will be called for interview, Whatsapp - 7825855974 (No calls only whatsapp message) for details We intend to hire 300 new medical coders each month. We recommend you to either enroll in a medical coding training institute or improve your knowledge in human anatomy and physiology on your own to be prepared for this opportunity. Please contact me once you are ready

Need Fresh graduate (Biomedical Engineering) Strong understanding of Human anatomy and physiology, Proficiency in medical terminology and ability to learn new terms quickly. Takehome salary - 15.2 K per month (After all deduction) + Yearly Bonus Work Location - Ambattur IE / Ramapuram No direct walk -in only shortlisted will be called for interview, Whatsapp - 7825855974 (No calls only whatsapp message) for details We intend to hire 300 new medical coders each month. We recommend you to either enroll in a medical coding training institute or improve your knowledge in human anatomy and physiology on your own to be prepared for this opportunity. Please contact me once you are ready

R.K.Hospital (Gajuwaka Hospitals Pvt. Ltd.,) is looking for Pharmacist to join our dynamic team and embark on a rewarding career journey Compounding and dispensing medications, as prescribed by physicians. Monitoring customers drug therapies, advising interventions, and informing customers of any potential side effects. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment. Completing operational requirements of t...

We are currently seeking a Pharmacovigilance Reporting Associate to join our diverse and dynamic team. As a Pharmacovigilance Reporting Associate at ICON, you will be responsible for the accurate and timely preparation of safety reports related to clinical trials and post-marketing activities. You will ensure compliance with regulatory requirements and contribute to the effective management of safety data to support patient safety and regulatory compliance. What You Will Be Doing: Preparing and reviewing safety reports, including periodic safety updates and individual case safety reports, ensuring accuracy and compliance with regulatory standards. Collecting and analyzing adverse event data ...

Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols, procedures, and study designs. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate in protocol development and review meetings with internal and external stakeholders. Job Requirements Strong knowledge of clinical trials, including design, conduct, and reporting. Excellent communication...

Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols, procedures, and study designs. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate in protocol development and review processes. Job Requirements Minimum 4 years of experience in clinical trials or a related field. Strong knowledge of clinical trial principles, practices, and regulation...

Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols, procedures, and study designs. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate in protocol development and review processes. Job Requirements Minimum 2 years of experience in clinical trials or a related field. Strong knowledge of clinical trial principles, practices, and regulation...

Job title : Sr. Associate HEVA (Evidence Synthesis) Hiring Manager: Head/Group Lead/Research Lead/Team Lead HEVA Location: Hyderabad % of travel expected: Travel required as per business need Job type: Permanent and Full time About the job Sanofi Global Hub is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. MedHub strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally. Main responsibilities: The overall purpose and main responsibilities are listed be...

We are looking for a highly skilled and experienced Clinical Trial Medical Advisor to join our team at Gratitude India Manpower Consultants Pvt. Ltd., with 32 years of experience in the IT Service & Consulting industry. Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols and procedures. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate ...

We are looking for a highly skilled Medical Writer with 2 to 5 years of experience to join our team in Mumbai. The ideal candidate will have a strong background in medical writing and excellent communication skills. Roles and Responsibility Develop high-quality written materials for various medical publications, including clinical trials and research studies. Collaborate with cross-functional teams to ensure accurate and timely delivery of written content. Conduct thorough research on medical topics and stay up-to-date with industry developments. Edit and proofread written content for clarity, grammar, and punctuation. Meet deadlines and deliver high-quality work under tight timelines. Parti...

Data Search & Analysis on the drug discovery and development Creating technology reports Kindly provide minimum two references with resume Required Candidate profile Keen interest in drug discovery, API Good Knowledge of organic chemistry Good Communication Skills

We require doctors for Medical Colleges & Hospitals Pan India Qualification : MD / MS / DNB / MCH (All Department ) 0-5 years of experience after MS/MD degree (any specialization) Position : Consultant , Senior Resident , Assistant Professor , Associate Professor , Professor Department : Clinical & Non Clinical Key-skills - Strong knowledge of Different Departments according to Qualification . Excellent communication skills for effective interaction with patients & colleagues. Ability to work efficiently under pressure during emergencies or critical situations Pooja Call/Whatsapp : 8837741438 Email Id - hr.wepsplacement@gmail.com

Roles and Responsibility Develop comprehensive, accurate, and engaging medical documents, including reports, articles, and presentations. Collaborate with cross-functional teams to ensure timely delivery of projects and meet deadlines. Conduct thorough research on various medical topics to stay updated with industry developments. Edit and proofread written content for clarity, grammar, and punctuation accuracy. Participate in brainstorming sessions to generate new ideas and concepts for content creation. Stay current with industry trends and advancements in medicine and healthcare. Job Requirements Minimum 5 years of experience in medical writing or a related field. Strong understanding of m...

Roles and Responsibility Develop high-quality written materials for various medical publications, including clinical trials and research studies. Collaborate with cross-functional teams to ensure accurate and timely delivery of written content. Conduct thorough research on medical topics and stay up-to-date with industry developments. Edit and proofread written content for clarity, grammar, and punctuation. Meet deadlines and deliver high-quality work under tight timelines. Participate in quality control processes to ensure consistency and accuracy in written materials. Job Requirements Strong knowledge of medical terminology and concepts, including anatomy, physiology, and pharmacology. Exc...