Director Regulatory Affairs Strategy

Job DescriptionJob DescriptionOur Pharmaceutical client seeks a Global Director Regulatory Affairs Strategy to guide global teams through the development and execution of regulatory strategy and the design of CMC components of drug development programs in collaboration with counterparts, investigators, project team members, and consultants. Lead/support...

PMV Pharmaceuticals Inc. Job Description: Executive Director, Head of Regulatory Affairs Reports to: Chief Development Officer Location: Hybrid (2 days a week in Princeton, NJ office)Position Overview The Executive Director, Head of Regulatory Affairs position will provide regulatory expertise and leadership to ensure that the company meets its objectives....

Job DescriptionJob DescriptionPMV Pharmaceuticals Inc.Job Description: Executive Director, Head of Regulatory AffairsReports to: Chief Development OfficerLocation: Hybrid (2 days a week in Princeton, NJ office)Position OverviewThe Executive Director, Head of Regulatory Affairs position will provide regulatory expertise and leadership to ensure that the...

The Head of US Medical - Endocrine Medical Affairs will report to the US General Manager with primary responsibility to lead the US Medical Directors and ensure the compliant execution of all medical programs and functions associated with the late-stage development and medical aspects of commercialization of endocrine assets at Ascendis Pharma. In addition...

Our client is looking to fill the role of Medical Affairs Consultant. This position will be fully remote.Responsibilities:Collaborating with Medical Affairs colleagues and external vendors to execute asset strategy and tactical plans with appropriate use of resources and according to developed timelinesTracking priority Medical Affairs tactics and...

We are looking for Pharma Business Analyst with Regulatory Experience for our client in Princeton, NJ Job Title: Pharma Business Analyst with Regulatory ExperienceJob Location: Princeton, NJJob Type: ContractJob Description:Pay Range: $60hr - $65hrRequirements:7+ years of experience as BA.Working knowledge of Pharmaceutical R&D Life Sciences.Specific...

10+ Years of experience is mandatory. The Business Analyst will engage and partner with cross-functional business teams to gather business requirements perform gap analysis develop functional requirements define solution recommendations draft business cases perform vendor research partner with internal and external development and testing teams to execute...

10+ Years of experience is mandatory. The Business Analyst will engage and partner with cross-functional business teams to gather business requirements perform gap analysis develop functional requirements define solution recommendations draft business cases perform vendor research partner with internal and external development and testing teams to...

Position: Associate Director, Biologics HCP Marketing Overview The role of Associate Director for Biologics Marketing requires a highly motivated and resourceful individual who has solid marketing acumen and leadership behaviors necessary to deliver brand strategic imperatives. Demonstrated success in health care professional (HCP) and patient marketing...

Job DescriptionJob DescriptionMMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable...

We’ve detected your location and are showing jobs in United States. Clear the filters to display jobs in all locations. Posted 1 day ago Clinical Trial Manager - Consultant - JOB ID: ELE24 Hybrid Palo Alto, California, United States ELE24 Posted 6 days ago Head of Regulatory Affairs, Oncology - Job ID: 1404 Hybrid Palo Alto, California, United States...

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Job DescriptionJob DescriptionAscendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology.Here at Ascendis, we pride ourselves on exceptional science, visionary leadership, and skilled and passionate...

Job Summary As a member of the Sourcing Execution team, you will play a pivotal role in overseeing and enhancing the sourcing operations within the organization. This position involves developing and executing sourcing strategies for Otsuka’s flexible workforce program. You will be responsible for managing vendor relationships, and driving continuous...

Regulatory Affairs Manager/ Personal Care Princeton, NJ, US Hybrid Are you passionate about the cosmetic and OTC sunscreen regulations in North America with a customer centric mindset? Join us in our journey! As a Regulatory Affairs Manager North Ame Technical Manager, Manager, Technical, Regulatory Affairs, Manufacturing, Business Services

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Director of CMC - Permanent - Princeton, NJProclinical is seeking a talented and motivated Director of CMC for a leading biotechnology company located in Princeton, NJ.Primary ResponsibilitiesThe successful candidate will play a crucial role in developing our overall API strategy, overseeing development activities, and managing CDMO partners. This role is...

The HEOR Consultant/VRWE Scientist serves as the lead for individual projects in support for HTA launch readiness projects for Nephrology products. Under the strategic lead of a Director, Health Outcomes, and working with cross-functional teams, the VRWE Scientist develops elements of a dossier, HE models, and Systematic lit reviews which will be used in...

The HEOR Consultant/VRWE Scientist serves as the lead for individual projects in support for HTA launch readiness projects for Nephrology products. Under the strategic lead of a Director, Health Outcomes, and working with cross-functional teams, the VRWE Scientist develops elements of a dossier, HE models, and Systematic lit reviews which will be used in...

The HEOR Consultant/VRWE Scientist serves as the lead for individual projects in support for HTA launch readiness projects for Nephrology products. Under the strategic lead of a Director, Health Outcomes, and working with cross-functional teams, the VRWE Scientist develops elements of a dossier, HE models, and Systematic lit reviews which will be used in...