🕒 July 9
Drug Safety Coordinator managing clinical information compliance and reporting at Cencora. Collaborating with clients for data accuracy and quality checks in the pharmaceutical industry.
🗣️🇫🇷 French Required
🕒 5 days ago
Pharmacovigilance Associate monitoring adverse events and safety risks for ICON, a global healthcare intelligence and clinical research organisation. Supporting regulatory reporting and safety investigations to help deliver medicines and medical devices to patients faster.
🕒 July 31
Graduate Pharmacovigilance Associate at ICON supporting safety monitoring and reporting of pharmaceutical products. Collaborating with teams on pharmacovigilance documentation and training activities in Poland.
🕒 July 29
Pharmacovigilance Associate at BioScript Solutions managing collection, processing, and reporting of adverse events. Ensuring compliance with safety regulations and providing support in pharmacovigilance activities.
🗣️🇫🇷 French Required
🕒 July 27
Senior Pharmacovigilance Specialist responsible for global operational delivery for an international pharma company. Managing audits, CAPAs, and coordinating Pharmacovigilance activities.
🕒 July 15
Independent Pharmacovigilance Officer at PrimeVigilance managing various case processing services with a strong focus on patient safety and collaboration.
🕒 July 15
Senior Pharmacovigilance Officer responsible for case processing and compliance in a collaborative environment at PrimeVigilance. Requires a life sciences background and strong communication skills.
🕒 July 15
Senior Pharmacovigilance Associate managing Individual Case Safety Reports at PrimeVigilance. Collaborating with global teams to ensure patient safety compliance across various locations.
🕒 July 15
Senior Pharmacovigilance Associate ensuring compliance with patient safety regulations. Processing ICSR reports and interacting with Quality Assurance at a global pharmacovigilance specialist.
🕒 July 15
Pharmacovigilance Officer managing case processing in pharmacovigilance at PrimeVigilance. Responsibilities include processing safety reports and mentoring junior employees with a life sciences background.
🕒 July 15
Senior Pharmacovigilance Associate managing ICSR processing and client support at PrimeVigilance. Collaborating with global teams to ensure patient safety and compliance with regulations.
🕒 July 15
Pharmacovigilance Specialist managing SAE data collection and reporting at Worldwide Clinical Trials. Ensuring regulatory compliance in a dynamic, global environment with a focus on patient safety.
🌐 United States, Brazil, +3 more countries – Remote
🌲 North Carolina – Remote
💵 $50k - $99k / year
⏰ Full Time
🟢 Junior
🦅 H1B Visa Sponsor
🕒 July 10
Drug Safety Associate II responsible for complex case management and regulatory collaboration at Corbus Pharmaceuticals. Leading pharmacovigilance efforts for innovative therapies in oncology and obesity.
🇬🇧 United Kingdom – Remote
💰 $46M Post-IPO Equity on 2020-02
⏰ Full Time
🟢 Junior
🟡 Mid-level
✨ Drug Safety Associate
🕒 July 10
Drug Safety Associate I at Corbus Pharmaceuticals processing ICSRs and managing regulatory submissions. Building in-house pharmacovigilance expertise in a high-growth biotech environment.
🍂 Massachusetts – Remote
💰 $46M Post-IPO Equity on 2020-02
⏰ Full Time
🟢 Junior
🟡 Mid-level
✨ Drug Safety Associate
🦅 H1B Visa Sponsor
🕒 July 10
Senior Safety Specialist performing Pharmacovigilance activities for a leading life sciences company. Joining a global team ensuring operational excellence in patient safety and compliance.
🕒 July 9
Pharmacovigilance Specialist managing compliance with safety information for Health Authorities. Requires fluency in English and Lithuanian and a life science degree.
🗣️🇱🇹 Lithuanian Required
🕒 July 6
Drug Safety Specialist II handling safety management plans and SAE case management at Precision for Medicine. Interfacing with sponsors and internal teams to ensure safety compliance and reporting.
🇺🇸 United States – Remote
💵 $75.6k - $113.4k / year
💰 $75M Private Equity Round on 2015-12
⏰ Full Time
🟢 Junior
🟡 Mid-level
✨ Safety Specialist
🕒 July 6
Drug Safety Specialist II handling safety management plans and SAE case management at Precision for Medicine. Interfacing with sponsors and internal teams to ensure safety compliance and reporting.
🇺🇸 United States – Remote
💵 $75.6k - $113.4k / year
💰 $75M Private Equity Round on 2015-12
⏰ Full Time
🟢 Junior
🟡 Mid-level
✨ Safety Specialist
+17 More Drug Safety Associate Jobs Available!
The average salary for remote drug safety associates is $0 per year. This is based on data from 6 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) | 6 | $0 |
We analyzed 3 job listings in the last year and found it takes about 17 days for employers to close a job opening.
We reviewed 6 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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