Full-Time Pharmacovigilance Scientist
Deciphera Pharmaceuticals is hiring a remote Full-Time Pharmacovigilance Scientist. The career level for this job opening is Experienced and is accepting Waltham, MA based applicants remotely. Read complete job description before applying.
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Deciphera Pharmaceuticals
Job Title
Pharmacovigilance Scientist
Posted
Career Level
Full-Time
Career Level
Experienced
Locations Accepted
Waltham, MA
Salary
YEAR $135000 - $189000
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Job Details
The Pharmacovigilance Scientist serves an integral role in safety data analyses for assigned investigational and/or marketed product(s) in partnership with the Safety Physician. She/he will support activities such as signal management, aggregate reports, RMP development, ad hoc safety query responses, literature surveillance, and other safety analyses; and must ensure deliverables are of high quality and are completed according to required timelines.
What You’ll Do:
- Coordinate and document signal management activities with the product Safety Physician. This includes performing signal evaluations and drafting signal evaluation reports.
- Prepare aggregate safety reports (e.g. DSURs, PADERs, PBRERs), including project management, database requests, data analysis, report authoring, assimilating information from other groups, review coordination, and quality checks.
- Support RMP updates and REMS reports as appropriate.
- Perform literature surveillance for marketed and investigational products .
- Prepare materials for Safety Committee meetings in conjunction with the product Safety Physician and document/archive meeting minutes and materials.
- Coordinate responses for ad hoc safety queries in conjunction with the Safety Physician and other cross-functional experts, including data analysis and authoring, as applicable.
- Support review and analysis of safety content for study protocols, CRFs, IB/RSIs, ICFs, SMPs, CSRs, DMC meetings, and coding reviews, as applicable.
- Demonstrate knowledge and stay up to date to ensure compliance with current and applicable global PV regulations and guidelines (e.g., CIOMS, EMA, FDA, ICH, etc.)
- Contribute to process improvement and consistency of cross-product processes.
- Maintain inspection readiness.
- Perform other tasks as assigned or required.
What You’ll Bring:
1+ years relevant medical, scientific/clinical, or pharmaceutical experience, including experience in drug safety serving in a PV Scientist or similar role.
Advanced degree (PharmD, RN, MD, PhD, MPH, NP, MS).
Demonstrated experience in analysis and interpretation of medical and scientific data.
Excellent oral and written communication skills.
Demonstrated ability to work effectively in a team environment as well as independently.
Ability to apply clinical judgment to interpret case information.
Knowledge of pharmacovigilance and drug development, including knowledge of applicable clinical trial and post-marketing safety regulations.
Familiarity with case processing, expedited reporting rules, and safety database concepts.
Proficiency with Microsoft Office Suite and Argus Safety systems.
Skills
FAQs
What is the last date for applying to the job?
The deadline to apply for Full-Time Pharmacovigilance Scientist at Deciphera Pharmaceuticals is
24th of September 2025
. We consider jobs older than one month to have expired.
Which countries are accepted for this remote job?
This job accepts [
Waltham, MA
] applicants. .
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