Regulatory Support Associate

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...

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...

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...

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...

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...

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...

The Specialist, Regulatory Operations - Submissions supports the development of submission plans created for regulatory submissions. This individual will be responsible for supporting the preparation, delivery, archiving and tracking of Promotional r Operations, Regulatory, Specialist, Operation, Management, Support, Manufacturing

Job Title: Senior Regulatory Operations Specialist About this role: The Senior Regulatory Operations Specialist position is an integral part of MRM for Health and the Regulatory Operations capability. Regulatory Operations is accountable and responsible for the preparation, review, and submission of regulatory packages to Client Medical, Legal and...

Job Title: Senior Regulatory Operations SpecialistAbout this role:The Senior Regulatory Operations Specialist position is an integral part of MRM for Health and the Regulatory Operations capability. Regulatory Operations is accountable and responsible for the preparation, review, and submission of regulatory packages to Client Medical, Legal and Regulatory...

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...

Provide support for faculty and staff located at the West Kentucky Research and Education Center located in Princeton KY. Skills / Knowledge / Abilities Internet Explorer; MS Office (Outlook, Word, Excel, Access, PowerPoint, Publisher, Front. Page); Support, Staff, Associate

**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...

summary Position Description: The QS Associate will supervise the activities with development, application, training, and maintenance of quality standards for industrial processes at Vytalogy Wellness. The QS Associate will also be assisting with ensuring that all products meet the established quality standard according to "The Code of Federal regulations...

Associate Director, EDT Documentation Lead, Early Development page is loaded Associate Director, EDT Documentation Lead, Early Development Apply locations Princeton - NJ - US time type Full time posted on Posted 30+ Days Ago job requisition id R1547188 At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through...

IND123 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 internally and with other members of SUN and its affiliates, including stakeholders as required. The Director will be responsible for ensuring ADE...

TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence.Our client, a leading pharmaceutical company is hiring a Clinical IRT Business Associate on a contract basis. Candidate MUST be located on the east coast. MUST have work experience in a health science or related IRT industry (pharmaceutical, hospital-based, laboratory,...

TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence.Our client, a leading pharmaceutical company is hiring a Clinical IRT Business Associate on a contract basis. Candidate MUST be located on the east coast. MUST have work experience in a health science or related IRT industry (pharmaceutical, hospital-based, laboratory,...

IND123 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 internally and with other members of SUN and its affiliates, including stakeholders as required. The Director will be responsible for ensuring ADE training...

Job DescriptionJob Description• Book in and Triaging of ICSRs• Perform data Entry of ICSRs in Pharmacovigilance database.• Entering source data in the database, Coding, Narrative(s) writing, and Generate Follow-up letters.• Generation of regulatory/partner submission reports and submission of cases.• Send follow-up/administrative queries.• Review...