Selected: ✨ Drug Safety Associate.
Selected: 🆕 Date Added.
🕒 Yesterday
Pharmacovigilance Associate managing adverse-event reporting and compliance for BioScript Solutions’ Canadian specialty-care programs. Supporting patient-focused pharmaceutical services remotely across Canada.
🗣️🇫🇷 French Required
🕒 3 days ago
Pharmacovigilance Associate monitoring adverse events and regulatory safety reports for ICON, a global healthcare intelligence and clinical research organization. Supporting signal detection and drug safety compliance.
🕒 6 days ago
Pharmacovigilance associate managing serious adverse events and patient safety for Veristat’s clinical research programs. Supporting safety reporting, training, databases, sponsors, and investigator sites.
🌐 United States, Canada – Remote
🍂 Massachusetts – Remote
💵 $74k - $85k / year
💰 Private equity on 2021-05
⏰ Full Time
🟢 Junior
🟡 Mid-level
✨ Associate
🦅 H1B Visa Sponsor
👻 Ghost score 0%
🕒 September 16
Associate Director overseeing pharmacovigilance and regulatory safety for Iambic Therapeutics’ AI-discovered oncology medicines. Managing vendors, safety data, inspections, and clinical development deliverables.
🇺🇸 United States – Remote
💵 $164k - $205k / year
💰 Series B on 2024-04
⏰ Full Time
🟠 Senior
👔 Director
👻 Ghost score 2%
🕒 September 15
Senior Pharmacovigilance Associate processing individual case safety reports for PrimeVigilance, a global pharmacovigilance specialist. Supporting safety reconciliations, regulatory compliance, coding, reporting, and client processes.
🕒 September 15
Senior Pharmacovigilance Associate processing safety reports and managing ICSR activities for PrimeVigilance, a global pharmacovigilance specialist. Supporting regulatory compliance and patient safety for pharmaceutical clients.
🕒 September 15
Senior Pharmacovigilance Associate processing safety reports and managing ICSR activities for PrimeVigilance, a global pharmacovigilance specialist. Supporting regulatory compliance and patient safety across pharmaceutical development and post-marketing surveillance.
🕒 September 15
Senior Pharmacovigilance Associate processing ICSRs, safety reports, and compliance data for PrimeVigilance’s global pharmacovigilance services. Supporting client reporting, reconciliation, coding, and local PV responsibilities.
🕒 September 15
Senior Drug Safety Specialist managing pharmacovigilance, safety reporting, and device vigilance for Emerald Clinical Trials’ global clinical research programs. Ensuring regulatory compliance, quality, and client delivery.
🕒 September 12
Graduate Pharmacovigilance Associate supporting adverse-event processing and safety reporting at ICON, a global healthcare intelligence and clinical research organisation. Home-based in Mexico City.
🕒 September 12
Graduate Pharmacovigilance Associate supporting adverse-event processing and safety reporting at ICON, a global healthcare intelligence and clinical research organisation. Maintaining pharmacovigilance documentation and regulatory compliance.
🕒 September 11
Senior Pharmacovigilance Associate managing drug-safety reporting, signal detection, and regulatory compliance. Supporting ICON’s global healthcare intelligence and clinical research mission to accelerate new medicines.
🕒 September 7
Drug Safety Officer managing local pharmacovigilance activities for TFS HealthScience, a global CRO. Supporting adverse-event reporting, regulatory compliance, audits, and clinical safety operations.
🗣️🇵🇱 Polish Required
🕒 August 29
Senior Pharmacovigilance Specialist managing global and local pharmacovigilance systems. Ensuring regulatory compliance, PV project delivery, safety reporting, and audit readiness for life sciences partners.
🕒 August 26
Pharmacovigilance Specialist serving as Local Safety Officer for DACH countries. Ensuring regulatory compliance, safety information processing, audits, literature monitoring, SOPs, and PV training.
🗣️🇩🇪 German Required
🕒 August 25
Pharmacovigilance Associate reviewing adverse events and regulatory reports for Orca Bio’s next-generation cell therapies. Supporting Argus case processing, vendor oversight, safety reporting, and clinical collaboration.
🇺🇸 United States – Remote
💵 $90k - $115k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
⚙️ Operations
🦅 H1B Visa Sponsor
👻 Ghost score 7%
🕒 August 21
Safety and pharmacovigilance specialist supporting medical-device safety reporting at Syneos Health, a life sciences services organization. Processing ICSRs, coding safety data, and supporting regulatory submissions.
🕒 August 20
Bilingual French Drug Safety Associate handling medical information and pharmacovigilance for Cencora’s Canadian pharma services. Supporting patient and provider programs through Innomar Strategies.
🇨🇦 Canada – Remote
💵 $43.5k - $77k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
💬 Bilingual
🚫👨🎓 No degree required
👻 Ghost score 18%
🗣️🇫🇷 French Required
🕒 August 13
Drug Safety Specialist conducting pharmacovigilance case processing for Thermo Fisher Scientific, a global life-sciences services and technology company. Reviewing safety cases, preparing regulatory reports, and coordinating clinical-trial safety activities.
🕒 August 12
Associate Safety Administrator supporting adverse-event documentation and clinical-trial coordination for Thermo Fisher Scientific. Managing safety records, training, reports, meetings, and project timelines.
🇵🇭 Philippines – Remote
⏰ Full Time
🟢 Junior
🟡 Mid-level
✨ Drug Safety Associate
🚫👨🎓 No degree required
👻 Ghost score 19%
+22 More Drug Safety Associate Jobs Available!


The average salary for remote drug safety associates is $60,255 per year. This is based on data from 11 job openings. Our advanced AI searches the internet for remote job openings and posts them on our website. We use the salary data from these job postings to calculate salary expectations.
Below is a breakdown of salary data by years of experience:
| Experience | Number of roles analyzed | Average Salary |
|---|---|---|
🟢 Junior Drug Safety Associate (1-2 yrs) | 11 | $60,255 |
We analyzed 8 job listings in the last year and found it takes about 28 days for employers to close a job opening.
We reviewed 11 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.
We scan the internet everyday and find jobs not posted on LinkedIn or other job boards.
We find jobs minutes after they're posted, so you can apply before everyone else.
Most members hear back within the first week
We find jobs other job boards miss.