Senior Pharmacovigilance Specialist - Boston

This Pharmacovigilance Specialist will be responsible for case processing and/or QC of clinical trial ICSRs and postmarket case processing from sanctioned countries. · ...

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 casesIncludes narrative writing, MedDRA coding, drafti ...

We are seeking a talented Pharmacovigilance Specialist to join our team at Rhythm. · As a PV Specialist with us you will have critical role shaping pharmacovigilance function/department evaluating safety patients receiving medications. · You will accountable day-to-day operationa ...

Kelly Science is seeking a Senior Pharmacovigilance Specialist for a growing company located in Boston MA. · ...

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

The Pharmacovigilance Scientist will support safety surveillance and signal management activities across clinical and post-marketing products. · This role partners closely with PV Physicians and cross-functional teams to manage risk, contribute to regulatory deliverables, and ens ...

This position is located in · Cambridge, MA and is hybrid with 2 days onsite required. · The Pharmacovigilance Case Processing Specialist will perform triage, intake, case entry, · and quality control (QC) of ICSRs from Biogen-sponsored clinical trials and assigned post-marketin ...

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 patients receiving Verastem manufactured products. · ...

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 core mission of the Verastem Safety & Pharmacovigilance group is to ensure patient safety for all patients receiving Verastem manufactured products. · Key Responsibilities: · Responsible for operational activities of ICSRs processed by PV case processing vendor. · Oversee day ...

Takeda Development Center Americas Inc is seeking a Medical Director Pharmacovigilance Rare Disease PDT with the following duties: serve as Global Safety Lead GSL and the Company-wide patient safety expert for assigned pharmaceutical biological drug device combined products accou ...

Takeda Development Center Americas, Inc. is seeking a Medical Director Pharmacovigilance, Rare Disease & PDT with the following duties: serve as Global Safety Lead (GSL) and the Company-wide patient safety expert for assigned pharmaceutical / biological / drug device combined pro ...

The Global Head of Pharmacovigilance and Safety Science is a strategic leadership role responsible for medical, strategic, and operational oversight of drug safety. · Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global r ...

+The Global Head of Pharmacovigilance and Safety Science is a strategic leadership role responsible for medical, strategic, and operational oversight of drug safety. · ...

The Product Specialist will drive adoption · & engagement for MadeAi across pharmaceutical, · medical device & healthcare clients.MadeAi Overview · MadeAi is a next-generation AI platform... · ...

We are seeking an experienced Senior Quality Systems & Compliance Specialist to support Quality Systems and Compliance activities within a regulated pharmaceutical environment. · ...

We are seeking a highly accomplished, board-certified physician-leader to serve as Chief Medical Officer (CMO). This pivotal role requires a specialist in medical oncology with deep experience in early- and mid-stage clinical development (Phase 1-3) of antibody therapeutics, targ ...

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

We are seeking an experienced Senior Quality Systems & Compliance Specialist to support Quality Systems and Compliance activities within a regulated pharmaceutical environment. · ...