Drug Safety Associate Salary in West Virginia

SAFETY & PHARMACOVIGILENCE SPECIALIST Candidate must be currently located in the DMV area 6 month temp to hire Location - Cambridge, MA (hybrid schedule) Medical experience and drug safety experience is Required Pharm D, Nursing MD or DO RESPONSIBILITIES • perform various tasks in support of clinical research including: adverse event analysis and processing, serious adverse event reconciliation • Preparation of IND safety reports for submission to the FDA • Safety document or data analysis • Clinical trial site support REQUIREMENTS • M.D. or D.O from an accredited institution • Infectious disease and/or oncology subspecialty highly preferred • Must have knowledge of GCP and ICH guidelines • Drug development/clinical trial experience essential • Knowledge of CTC and/or MedDRA coding preferred • Experience leading clinical and cross functional teams is a plus • Must have excellent oral, written, presentation and computer skills • 3+ years of pharmaceutical or biotech industry or academic

SAFETY & PHARMACOVIGILENCE SPECIALIST Candidate must be currently located in the DMV area 6 month temp to hire Location - Cambridge, MA (hybrid schedule) Medical experience and drug safety experience is Required Pharm D, Nursing MD or DO RESPONSIBILITIES perform various tasks in support of clinical research including: adverse event analysis and processing, serious adverse event reconciliation Preparation of IND safety reports for submission to the FDA Safety document or data analysis Clinical trial site support REQUIREMENTS M.D. or D.O from an accredited institution Infectious disease and/or oncology subspecialty highly preferred Must have knowledge of GCP and ICH guidelines Drug development/clinical trial experience essential Knowledge of CTC and/or MedDRA coding preferred Experience leading clinical and cross functional teams is a plus Must have excellent oral, written, presentation and computer skills 3+ years of pharmaceutical or biotech industry or academic experience Beacon Hill

A pharmaceutical company in New Jersey is looking to add a new Senior Pharmacovigilance Associate to their growing team. In this role, the Senior Pharmacovigilance Associate will be responsible for monitoring, processing, controlling, and reporting individual case safety reports and aggregate safety reports for company products. Responsibilities: The Senior Pharmacovigilance Associate will: Review individual case safety reports (ICSR) ensuring that adverse event reports are processed in a timely manner, in accordance with the appropriate company SOPs, study protocols, and within regulatory timelines Assist with data-lock reconciliations and ensure all cases are complete and all outstanding queries are resolved and closed Provide pharmacovigilance input on essential study documentation from (study protocols, clinical trial agreement, safety management plan, clinical trial agreement, informed consent form, case report forms, protocol amendments and study reports) Remain up to date on all

3-5 years drug safety or clinical safety experience – Required A clinical degree (e.g., RPh/PharmD, BSN, RN) – Required Two years clinical experience in a medical setting, demonstrate general medical and pharmacology knowledge – Required Prior experience in drug safety within the pharmaceutical or biotechnology industry. In-depth knowledge of global pharmacovigilance regulations, including FDA, EMA, and ICH guidelines. Strong analytical skills with the ability to interpret and evaluate complex scientific data. Excellent communication skills, both written and verbal, with the ability to effectively

Are you an experienced Pharmacovigilance Associate with a desire to excel? If so, then Talent Software Services may have the job for you! Our client is seeking an experienced Pharmacovigilance Associate to work in South San Francisco, CA. Position Summary: PV Clinical Associate performs the tactical and operational job responsibilities, including but not limited to the collection, clinical review, evaluation, and processing of adverse event (AE) information received by US Drug Safety. The PV Clinical Associate leads clinical review of USDS cases (processed in-house or externally by the vendor) and supports the US Drug Safety PV Clinical Manager - Associate in all activities. All responsibilities are performed under the direction of the PV Clinical Manager- Associate. Primary Responsibilities/Accountabilities: Completes drug safety monitoring and tracking in a timely, thorough and accurate manner in accordance with pharmacovigilance (PV) and related standards, regulations and /Roche Sta

Are you an experienced Pharmacovigilance Associate with a desire to excel? If so, then Talent Software Services may have the job for you! Our client is seeking an experienced Pharmacovigilance Associate to work in South San Francisco, CA. Position Summary: PV Clinical Associate performs the tactical and operational job responsibilities, including but not limited to the collection, clinical review, evaluation, and processing of adverse event (AE) information received by US Drug Safety. The PV Clinical Associate leads clinical review of USDS cases (processed in-house or externally by the vendor) and supports the US Drug Safety PV Clinical Manager - Associate in all activities. All responsibilities are performed under the direction of the PV Clinical Manager- Associate. Primary Responsibilities/Accountabilities: Completes drug safety monitoring and tracking in a timely, thorough and accurate manner in accordance with pharmacovigilance (PV) and related standards, regulations and /Roche Sta