Drug Safety Associate jobs
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- Revolite Infotech Pvt. LtdRemote
- Flexible schedule
- We are looking for experienced Pharmacology and Drug Safety professionals to evaluate AI-generated scientific content related to pharmacokinetics,…
- Cliniweb ServicesPune, Maharashtra
- Paid time off
- Paid sick time
- Cell phone reimbursement
- Provident Fund
- Perform data entry into pharmacovigilance safety databases.
- Conduct medical literature screening for safety-related information.
- SoteriusRemote
- Acquiring comprehensive knowledge of the product portfolio and safety profiles for products across therapeutic areas.
- Line management for assigned personnel.
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- SoteriusNoida, Uttar Pradesh
- Support in the area of drug safety and pharmacovigilance activities as requested by the management.
- Record and review adverse drug reactions in the safety…
- Innovative Pharmaceuticals Pvt LtdSatara District, Maharashtra
- Identify and assess adverse drug reactions and safety information.
- This is an excellent opportunity for freshers who want to start their career in the *…
- JeevanHyderabad, TelanganaJob Designation: Drug Safety Associate Experience: 0 to 2 years Location: Hyderabad Email: Hr@jeevanscientific…
- JeevanHyderabad, TelanganaJob Designation: Drug Safety Associate Experience: 0 to 2 years Location: Hyderabad Email: Hr@jeevanscientific…
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- Statistical InsightsPune, Maharashtra
- Internet reimbursement
- Responsible for review of investigational new drug safety reports (INDSR) and submission to FDA (as applicable).
- ParexelRemote
- Support safety-related regulatory activities such as aggregate reports and urgent safety updates.
- An Associate must be technically competent and continually…
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- Fidelity Health ServicesMumbai, Maharashtra
- Experience in exchanging safety data / conducting reconciliations with business partners.
- Timely exchange of safety data with partners and conduct adverse event…
View similar jobs with this employerAccentureChennai, Tamil Nadu- These services ensure the safety and efficacy of medications by monitoring and analyzing data from clinical trials, healthcare providers, and patients.
- JeevanHyderabad, TelanganaJob Designation: Sr. Drug Safety Associate Experience: 3 to 5 Years Location: Hyderabad Email: Hr@jeevanscientific…
- Continuum IndiaChandigarh
- Periodic Benefit Risk Evaluation Reports (PBRERs)/ Periodic Safety Update Reports (PSURs), Addendum to Clinical Overviews (ACOs), Addendum PSURs, PSUR Line…
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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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- KLINSCIENCE HEALTHCAREPune, Maharashtra
- Paid sick time
- Provident Fund
- Flexible schedule
- Professionals in this field protect public health by monitoring drug safety across clinical trials and post-market use.
- Pay: Up to ₹340,000.00 per year.
- View all KLINSCIENCE HEALTHCARE jobs - Pune, Maharashtra jobs
- Salary Search: Pharmacovigilance salaries
Job Post Details
AI Response Evaluator – Pharmacokinetics & Drug Safety Specialist - job post
₹300 - ₹500 an hour
Job details
Pay
- ₹300 - ₹500 an hour
Job type
- Contractual / Temporary
- Freelance
Benefits
Pulled from the full job description
- Flexible schedule
Full job description
Job Title: AI Response Evaluator – Pharmacokinetics & Drug Safety Specialist
Location: Remote
Job Type: Freelance / Contract
Job Summary:
We are looking for experienced Pharmacology and Drug Safety professionals to evaluate AI-generated scientific content related to pharmacokinetics, pharmacodynamics, clinical trials, adverse events, and pharmacovigilance.
Key Responsibilities:
- Review AI-generated responses for scientific accuracy and clinical relevance
- Evaluate content related to Pharmacokinetics (PK), Pharmacodynamics (PD), Drug Safety, Clinical Trials, and Risk Management
- Identify inaccuracies and provide expert feedback
- Annotate and improve AI responses using structured evaluation frameworks
- Ensure compliance with scientific and regulatory standards
Required Qualifications:
- MSc or higher in Pharmacology, Pharmaceutical Sciences, Clinical Pharmacy, or Toxicology
- Strong experience in Drug Safety and Pharmacovigilance
- Experience in Clinical Trial Safety Monitoring preferred
- Knowledge of ICH, FDA, and EMA regulations
- Experience using RTB and/or PharmaPendium databases
Preferred Qualifications:
- Pharmacovigilance quality review or audit experience
- Experience with AI, NLP, data annotation, or content evaluation projects
- Strong analytical and scientific writing skills
Key Skills:
- Pharmacovigilance
- Drug Safety
- Clinical Trials
- PK/PD
- Risk Management
- Regulatory Compliance
- Scientific Literature Review
- Medical Content Evaluation
Pay: ₹300.00 - ₹500.00 per hour
Benefits:
- Flexible schedule
Work Location: Remote
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