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- SoteriusRemote
- Serve as a safety scientist on the medical safety team and participate in signal detection, risk management, mitigation plans, and safety analyses for aggregate…
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- ThermaissanceDelhi, Delhi
- Health insurance
- Paid time off
- Paid sick time
- Provident Fund
- Work from home
- Competitive compensation with strong growth opportunities in a high-impact medical device innovation company..
- Design and execute clinical studies.
- BaxterBengaluru, Karnataka
- Paid time off
- Develop knowledge and understanding of ISO 10993 series of standards for executing biological assays and toxicological risk assessments per ISO 10993-17 for…
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- BaxterBengaluru, Karnataka
- Paid time off
- Develop knowledge and understanding of ISO 10993 series of standards for executing biological assays and toxicological risk assessments per ISO 10993-17 for…
- View all Baxter jobs - Bengaluru, Karnataka jobs - Associate Scientist jobs in Bengaluru, Karnataka
- Salary Search: Assoc Scientist I salaries in Bengaluru, Karnataka
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- Solar One EnergyNoida, Uttar Pradesh
- Support development of biotech / medical device / therapeutic products.
- We are looking for a Biotechnologist / Pharma Technologist who can drive research and…
- Will be responsible for executing medical affairs strategy in the assigned zone.
- Provide medical and product expertise towards registration of new products/…
- View all BI India jobs - Delhi jobs - Liaison jobs in Delhi
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- SoteriusRemote
- Provide medical and PV oversight and input to Protocols, Investigator brochures,.
- Medical Review of aggregate reports (PBRER/DSUR/PADER) and related signal.
- View all Soterius jobs - Remote jobs - Physician jobs in Remote
- Salary Search: Global Medical Safety Physician salaries in Remote
- AEVEVO TECHNOLOGY PRIVATE LIMITEDChennai, Tamil Nadu
- Represent Mednevo at medical conferences and among the doctor community.
- Regulatory & Quality: Ensure compliance with healthcare regulations, data privacy (…
- NovartisDelhi
- Implement clinical and educational strategies and respond to unsolicited medical enquiries.
- Works within Ethics and Compliance policies -Achievement of annual…
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- NovartisDelhi
- Implement clinical and educational strategies and respond to unsolicited medical enquiries.
- Works within Ethics and Compliance policies -Achievement of annual…
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- Salary Search: Medical Science Liason salaries
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- Continuum IndiaChandigarh
- Good knowledge of medical terminology, fluency in written and spoken English, computer proficiency, an ability to work with web-based applications, and…
- View all Continuum India jobs - Chandigarh jobs - Scientist jobs in Chandigarh
- Salary Search: Pharmacovigilance Scientist salaries in Chandigarh
- Thermo Fisher ScientificBengaluru, Karnataka
- Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.).
- Active participation in team meetings.
- Katalyst Healthcares & Life SciencesGuntur, Andhra Pradesh
- The Research Scientist, AIML & Drug Discovery Research Staff will apply artificial intelligence, machine learning, data science, bioinformatics, and…
- Helax healthcare pvt.ltd.Roorkee, UttarakhandNeed Pharmacovigilance astt M PHARMA FOR pharmaceutical manufacturing company Pay: ₹15,000.00 - ₹32,991.06 per month Work Location: In…
- NiramaiBengaluru, Karnataka
- Relevant experience of 7 – 15 years in a pharma or medical devices company.
- Partner with Heads of Business, Technology, Research and Product to design…
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- Udbhava Avinya Bharat LLPRemote
- Work from home
- Familiarity with regulatory standards for medical or sustainable products.
- This role sits at the intersection of *material science, sustainability, and…
Job Post Details
Global Medical Safety Scientist - job post
Remote
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Job details
Job type
- Full-time
Full job description
Job Description:
Position Summary
Scientific function responsible to support a global pharmacovigilance system (both development and post marketing). Scientific functions include but not limited to signal detection, risk assessment and management, Risk Management Plan (RMP) development, aggregate safety reporting, and clinical safety surveillance.
Key Job Responsibilities-
- Ensure that the benefit-risk assessment is current and that any changes are as per governance principles.
- Ensure patient safety for company’s products and maintenance of compliance with the Pharmacovigilance regulations of Regulatory Agencies around the globe
- Timely completion of PV Assessment activities through product development, product maintenance and lifecycle management.
- Serve as a safety scientist on the medical safety team and participate in signal detection, risk management, mitigation plans, and safety analyses for aggregate reports and Health Authority responses.
- Participate in non-ICSR literature surveillance
- Ensure timely review, approval and communication of findings via SMT and governance forums.
Qualifications
Required:
Excellent communication and interpersonal skills and experience in mentoring others- Demonstrated qualities of competency, accountability, initiative, and leadership
- Experience in process improvement initiatives
- Extensive knowledge of US, ICH and EU PV and GCP regulations
- Experience with Risk Management and Signal Detection preferred
- Excellent strategic decision-making and analytical skills
- Strong leadership skills with excellent track record
- Computer skills including proficiency in use of Microsoft Word, Excel & PowerPoint
- Strong verbal, writing and organizational skills, including a good command of English
- Experience with Regulatory Authority Inspections (PV and GCP); experience managing vendors
- Medical writing experience
Education and Related Experience
- Graduate degree in health sciences, nursing, pharmacy, public health, epidemiology or other relevant health-related field (MD, PhD, PharmD, NP, PA, pharmacy or nursing degree) with at least 4 years of experience in clinical, pharmacological, or related fields of expertise
OR
- Bachelor’s degree in health sciences, nursing, pharmacy, public health, epidemiology or other relevant health-related field plus 10+ years of relevant experience in drug safety/pharmacovigilance, or related fields in the pharmaceutical industry.
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