Head of Drug Safety - Somerville

· Director, Drug Safety & PharmacovigilanceAt Merida Biosciences, 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 comple ...

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). · ...

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 · ...

· Company Description · IRI believes in commitment, integrity and strategic workforce solutions. · Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business ...

Responsible for case processing and/or QC of clinical trial ICSRs and postmarket 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). · 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 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 ...

+ · 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 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 ...

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 · ...

Centessa Pharmaceuticals plc (Nasdaq: CNTA) new kind of pharmaceutical company with a deconstructed R&D environment that prioritizes data driven decision making led by subject matter experts. Centessa is advancing a portfolio of high conviction programs with strong biological val ...

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. · ...

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 ...

+Job summary · A clinical-stage biopharmaceutical company dedicated to creating extraordinary medicines. The Director, Drug Safety Operations/Pharmacovigilance (PV) will lead and oversee safety reporting activities across clinical programs.Responsibilities · +• Oversee all safety ...

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 ...

Join our team as a Drug Safety Consultant I where you'll collaborate with global stakeholders to manage and execute safety data exchange agreements (SDEAs) · ...

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

Join our team as Drug Safety Consultant I where you’ll collaborate with global stakeholders to manage safety data exchange agreements. · Collaborate with stakeholders to assess SDEA execution and compliance<li_review corporate agreements author revise execute SDEAs<li Identify re ...