Selected: ⨠Drug Safety Associate.
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Selected: đ Date Added.
đĽ 10 hours ago
Pharmacovigilance specialist monitoring adverse events and regulatory compliance for WEP Clinicalâs clinical research programs. Managing safety reports, audits, metrics, and Argus database activities.
đ Romania, Croatia â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ§Ş Clinical Research
đť Ghost score 10%
đĽ 10 hours ago
Pharmacovigilance specialist managing adverse-event reporting and compliance for WEP Clinicalâs clinical research programs. Supporting regulatory submissions, audits, safety metrics, and global site coordination.
đ¨đŚ Canada â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ§Ş Clinical Research
đť Ghost score 10%
đ 4 days ago
Senior Pharmacovigilance Associate managing adverse event reporting, safety signals, and regulatory submissions. Supporting ICONâs sponsor-dedicated clinical research and pharmaceutical safety programs.
đ 5 days ago
Regional pharmacovigilance officer overseeing literature surveillance, safety reporting and regulatory compliance across Latin American markets for Siteroâs life sciences services.
đ˛đ˝ Mexico â Remote
âł Contract/Temporary
đĄ Mid-level
đ Senior
đ§Ş Clinical Research
đť Ghost score 10%
đŁď¸đŞđ¸ Spanish Required
đŁď¸đ§đˇđľđš Portuguese Required
đ October 31
Drug safety case processing consultant supporting pharmaceutical, medical device, and consumer care innovators. Managing safety cases, regulatory compliance, and pharmacovigilance data quality.
đ§đˇ Brazil â Remote
âł Contract/Temporary
đĄ Mid-level
đ§Ş Clinical Research
đť Ghost score 10%
đŁď¸đŻđľ Japanese Required
đ October 30
Senior Pharmacovigilance Manager leading complex drug-safety projects for iVigee, a physician-led pharmacovigilance company. Overseeing regulatory compliance, audits, client delivery, and PV team development.
đ October 29
Pharmacovigilance Specialist processing adverse-event cases for ProPharmaâs biotech, medical-device, and pharmaceutical clients. Coding MedDRA cases, preparing narratives, and supporting global safety compliance.
đ United Kingdom, Serbia, +2 more countries â Remote
đ° $8.6M Venture Round on 2020-10
â° Full Time
đ˘ Junior
đĄ Mid-level
đ§Ş Clinical Research
đŹđ§ UK Skilled Worker Visa Sponsor
đť Ghost score 10%
đ October 29
Drug Safety Associate supporting Cencoraâs Canadian patient support and pharma commercialization services. Processing adverse events, quality complaints, clinical data, and pharmacovigilance reports.
đ¨đŚ Canada â Remote
â° Full Time
đ˘ Junior
đĄ Mid-level
đ§Ş Clinical Research
đť Ghost score 10%
đŁď¸đŤđˇ French Required
đ October 28
Graduate Pharmacovigilance Associate supporting adverse-event review and safety reporting. Contributing to pharmaceutical safety documentation and regulatory compliance at ICON.
đ October 26
Pharmacovigilance Associate supporting adverse-event reporting and regulatory safety compliance for Harrowâs ophthalmic pharmaceutical portfolio. Processing ICSRs, FDA submissions, and aggregate safety reports.
đď¸ New Jersey â Remote
đ° $100M Post-IPO Debt on 2023-03
â° Full Time
đ˘ Junior
đĄ Mid-level
⨠Associate
đť Ghost score 12%
đ October 21
Patient Safety Associate processing drug safety reports, regulatory submissions, and literature reviews. Supporting Parexelâs global clinical development and pharmacovigilance services.
đşđ¸ United States â Remote
đ° Venture Round on 1990-01
â° Full Time
đ˘ Junior
đĄ Mid-level
⨠Drug Safety Associate
đŚ H1B Visa Sponsor
đť Ghost score 10%
đ October 17
Pharmacovigilance Specialist processing clinical-trial safety cases and regulatory reports for Biomapas. Ensuring pharmacovigilance compliance across any EU country.
đ Bulgaria, Croatia, +3 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
⨠Clinical Specialist
đť Ghost score 10%
đ October 12
Senior Pharmacovigilance Associate processing ICSRs, safety reports, and regulatory data for PrimeVigilanceâs global pharmaceutical clients. Supporting pharmacovigilance operations and patient safety across clinical and post-marketing activities.
đ October 12
Senior Pharmacovigilance Associate processing individual case safety reports for PrimeVigilance, a global pharmacovigilance specialist. Supporting regulatory compliance, safety data analysis, reporting, and patient protection.
đ October 10
Graduate Pharmacovigilance Associate supporting adverse-event processing and safety reporting at ICON, a global clinical research services organization. Maintaining pharmacovigilance documentation and regulatory compliance.
đ October 9
Drug Safety Associate managing SAE processing, Argus documentation, and pharmacovigilance compliance for biotechnology company Exelixis. Overseeing study safety operations, vendors, reporting, and cross-functional collaboration.
đşđ¸ United States â Remote
đľ $130.5k - $185k / year
đ° $65M Post-IPO Equity on 2012-02
â° Full Time
đ Senior
đ´ Lead
⨠Drug Safety Associate
đŚ H1B Visa Sponsor
đť Ghost score 0%
đ October 9
Senior Associate Pharmacovigilance supporting SAE oversight and regulatory reporting at Worldwide Clinical Trials, a global CRO. Leading safety activities for clinical studies in Brazil-based remote work.
đ October 8
Pharmacovigilance Specialist managing safety cases, literature screening, and PV reporting for Delta PV. Translating Turkish adverse events and supporting client reconciliations remotely in Turkey.
đŁď¸đšđˇ Turkish Required
đ September 29
Pharmacovigilance Analyst managing local drug-safety operations for Cencora in Brazil. Maintaining safety systems, reports, procedures, training, audits, and regulatory risk measures.
đ September 22
Pharmacovigilance Associate managing adverse-event reporting and compliance for BioScript Solutionsâ Canadian specialty-care programs. Supporting patient-focused pharmaceutical services remotely across Canada.
đŁď¸đŤđˇ French Required
+23 More Drug Safety Associate Jobs Available!


We analyzed 14 job listings in the last year and found it takes about 27 days for employers to close a job opening.
We reviewed 19 job postings and found the top 10 skills employers are asking for most often are:
You need strong analytical and critical thinking skills, attention to detail, knowledge of pharmacovigilance processes, and proficiency in data analysis tools. Additionally, good communication and teamwork skills are important for remote collaboration.
Typically, a degree in life sciences, pharmacy, or a related field is required. Relevant experience in drug safety or clinical trials is highly valued. Certifications in pharmacovigilance or related areas can enhance your qualifications.
Responsibilities include monitoring and evaluating adverse events, maintaining safety databases, preparing safety reports, and collaborating with regulatory agencies. You will also need to ensure compliance with industry regulations and internal policies.
Benefits include flexible work schedules, the ability to work from any location, reduced commuting time, and improved work-life balance. Remote positions also offer opportunities to work with global teams and gain diverse experience in the pharmaceutical industry.
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