Safety director jobs in Princeton, New Jersey (NJ) State

As an Associate Director of Drug Safety and Pharmacovigilance Scientist, you will become part of the Global Drug Safety and Pharmacovigilance department, where you will be responsible for drug related activities in close cooperation with Safety colleagues along with cross-functional team members....

As our Associate Director, you must effectively implement Signal Management Group surveillance strategies for proactive and systematic detection and evaluation of new safety signals and emerging trends from clinical and post-marketing safety data for complex pharmaceutical products (e. ...

As an Associate Director of Drug Safety and Pharmacovigilance Scientist, you will become part of the Global Drug Safety and Pharmacovigilance department, where you will be responsible for drug related activities in close cooperation with Safety colleagues along with cross-functional team members....

***Must reside in or within a commutable distance from assigned territory (New York City, Long Island, and Northern NJ)*** Who We Are: As a global leader in smart, healthy and sustainable buildings, our mission is to reimagine the performance of buildings to serve people, places and the planet. ...

Associate Director/Director, Drug Safety and Pharmacovigilance Physician. Analyse and produce safety evidence and perform safety & efficacy analyses to support the overall plans for the team. Interpret clinical trial safety data for clinical trial reports and submission documents. Ensure patient ...

Track the development, testing, implementation and closure of all PV Systems requests. Assist PV Systems Director with the following activities:. PV business unit, the primary focus is the Argus Safety Systems. At least 4 years of experience in Pharmacovigilance Systems with at least 2 years of e...

The Drug Safety & Pharmacovigilance (GDS&PV) Physician role is a safety expert medical role contributing to the global safety strategy and overall safety profile for the assigned Genmab products (mainly investigational) throughout their lifecycle. You will work together with other Drug Safet...

Leadership and ownership of internal safety governance bodies (Safety Management Team, Joint Safety Management Team) Active contribution to internal andexternal forums (e g. Company Core Data Sheet, ad hoc aggregate safety reports, periodic safety. Contribution and review of safety documents from...

The Drug Safety & Pharmacovigilance (GDS&PV) Physician role is a safety expert medical role contributing to the global safety strategy and overall safety profile for the assigned Genmab products (mainly investigational) throughout their lifecycle. You will work together with other Drug Safety sta...

Senior Director Drug Safety and Pharmacovigilance. Develop strategies, working with the Head of Safety, to achieve PV Medical Safety goals. Assess safety signals and trends and proactively manage any potential safety issues. Accountable for medical evaluation/interpretation of aggregate safety da...

The Pilot Plant Director may delegate to him the overseeing of the Pilot Plant Cost Center's annual ... call reports and other important documents * Member of Engineering Safety sub-committee * Interact ...

Targeting 12 years of relevant drug safety experience in the biotechnology/pharmaceutical industry, including safety leadership experience. ...

Develop Drug Safety Standard Operating Procedures and ensure training for Drug Safety personnel. The Associate Director/ Director, Drug Safety (Title is comensurate with experience) will oversee and implement operations of Pharmacovigilance in North America and communicate relevant information in...

Executive Director, Facilities Information Technology. This Executive Director, Facilities Information Technology is accountable for managing and ensuring the 24 x 7, end to end reliability, security, and operational integrity of critical life, safety systems for the campus and additional special...

The Drug Safety & Pharmacovigilance (GDS&PV) Physician role is a safety expert medical role contributing to the global safety strategy and overall safety profile for the assigned Genmab products (mainly investigational) throughout their lifecycle. You will work together with other Drug Safet...

Targeting 10 years of progressive applied epidemiology experience in a regulated biotechnology or pharmaceutical industry required or PhD with 4 years of progressive applied epidemiology experience. ...

Targeting 10 years of progressively experience in the pharmaceutical or biotech industry with majority in Pharmacovigilance. ...

Job DescriptionJob DescriptionDirector, Safety - Process Optimization & Training: Medical Device Vigilance ExpertGilead Sciences, Inc. The Patient Safety (PS) department is a global function that is part of the Development organization within Gilead. Gilead Sciences is seeking an ambitious indivi...

This role will have the medical safety expertise to perform obligatory safety functions with oversight from global drug safety lead. Lead the development of safety risk management plans, safety components of IND/NDA/MAA filings, annual safety reports. Ensuring safety of products through the produ...

As an Associate Director of Drug Safety and Pharmacovigilance Scientist, you will become part of the Global Drug Safety and Pharmacovigilance department, where you will be responsible for drug related activities in close cooperation with Safety colleagues along with cross-functional team members....

As an Associate Director of Drug Safety and Pharmacovigilance Scientist, you will become part of the Global Drug Safety and Pharmacovigilance department, where you will be responsible for drug related activities in close cooperation with Safety colleagues along with cross-functional team members....

Join a Legacy of Innovation 110 Years and Counting!.Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology...

As an Associate Director of Drug Safety and Pharmacovigilance Scientist, you will become part of the Global Drug Safety and Pharmacovigilance department, where you will be responsible for drug related activities in close cooperation with Safety colleagues along with cross-functional team members....

Reporting to the Vice President of the Diagnostics and Genomics (DGG) Quality organization within Global Quality and Regulatory Affairs (GQRA), the Director of Clinical and Safety Quality Assurance will be responsible for setting strategy for and leading the Clinical and Safety Quality Assurance ...