Sr. Scientist, Drug Safety - Boston, MA

We are seeking a Scientist to support pharmacovigilance activities across Centessa's clinical-stage development programs. · RN or bachelor's degree in health sciences or related field required. · ...

We are seeking a Scientist, Drug Safety (Pharmacovigilance) to support pharmacovigilance activities across Centessa's clinical-stage development programs. · RN or bachelor's degree in health sciences or related field required. · 5+ years of experience in drug safety in the biotec ...

We are seeking a Scientist Drug Safety Pharmacovigilance to support pharmacovigilance activities across Centessa s clinical stage development programs. · Conduct scientific review and evaluation of ICSRs · ...

The core mission of the Verastem Safety & Pharmacovigilance group is to ensure patient safety for all patients receiving Verastem manufactured products. · This is done by ensuring that the safety profile of Verastem products remains accurate and up to date throughout the product ...

The core mission of the Verastem Safety & Pharmacovigilance group is to ensure patient safety for all patient's receiving Verastem manufactured products. · This is done by ensuring that the safety profile of Verastem products remains accurate and up to date throughout the product ...

The job requires a drug safety consultant to process and QC clinical trial ICSRs and post-market case processing from sanctioned countries. · 4+ years experience in pharmacovigilance · ...

Responsible for case processing and/or QC of clinical trial ICSRs and post-market case processing from sanctioned countries. · ...

This position will work with cross-functional internal and external global stakeholders of all levels to execute safety data exchange agreements (SDEAs). · ...

Job summary · We are pioneering true precision medicines for antibody-driven diseases. We specifically target pathogenic antibodies and their cellular sources with bespoke Fc biotherapeutics engineered to selectively and completely eliminate the root causes of autoimmune and alle ...

+ · Responsible for case processing and/or QC of clinical trial ICSRs and postmarket case processing from sanctioned countries. · +Triage, Intake, case entry and QC of ICSRs originating from *** sponsored studies or other assigned cases · Narrative writing, MedDRA coding, drafti ...

This position involves case processing and/or QC of clinical trial ICSRs and postmarket case processing from sanctioned countries. · Triage, Intake, case entry and QC of ICSRs originating from Biogen sponsored studies or other assigned casesIncludes narrative writing, MedDRA codi ...

The Safety and Benefit Risk, Global Case Management department performs pharmacovigilance activities, ensuring timely adverse event reporting in compliance with applicable laws and regulations/company policies throughout the lifecycle of products. · ...

Responsible for case processing and/or QC of clinical trial ICSRs and post market case processing from sanctioned countries. · Knowledge of Global and local safety regulations · Excellent written and verbal communication skills · Experience in ICSR processing in safety database s ...

This position will work with cross-functional internal and external global stakeholders of all levels to execute safety data exchange agreements (SDEAs). · Outreach and collaboration with different stakeholders to assess the need and support the execution and compliance of SDEAs. ...

Responsible for case processing and/or QC of clinical trial ICSRs and postmarket case processing from sanctioned countries. · ...

We are seeking a Senior Scientist to support pharmacovigilance activities across Centessa's clinical-stage development programs. · ...

The Senior Director of Drug Safety & Pharmacovigilance Operations will lead Kymera's global pharmacovigilance (PV) and safety , ensuring robust safety surveillance, · compliance, and operational excellence across all programs.This leader will oversee the collection, · evaluation, ...

+We are seeking a Senior Scientist, Drug Safety (Pharmacovigilance) to support pharmacovigilance activities across Centessa's clinical-stage development programs. · +Provide advanced scientific oversight of ICSR and clinical trial SAE evaluation... · +PharmD or PhD in scientific ...

The Director, Drug Safety Operations/Pharmacovigilance (PV) will lead and oversee safety reporting activities across clinical programs, ensuring compliance with global regulatory requirements. · Oversee all safety reporting activities managed by CROs and consultants. · Serve as t ...

We are focused on results driven by rigor logic outcomes innovation passion compassion for wellbeing people. · ...