Average salary: $63,764 /yearly
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...Responsibilities:
ROLE AND RESPONSIBILITIES:
Manage Lupins existing REMS programs and help in the development of new... ...operations
Responsible for maintaining and updating various regulatory databases to ensure accuracy of information
Any additional responsibilities...
Suggested
...disability insurance, vacation, and tuition reimbursement.
Job Summary:
Manages company programs and policies to ensure that the organization complies with government, customer, and company regulatory requirements. Prepares and distributes compliance status reports to...
Suggested
Temporary work
Manage Lupin's existing REMS programs and help in the development of new REMS programs (as needed) with the support of the supervisor... ...REMS and other patient safety programs. Works closely with Phar Regulatory Affairs, Manager, Regulatory, Operations, Product Development,...
Suggested
SUMMARY OF POSITION Manages team and leads Regulatory Associates and/or Senior Regulatory Associates in regulatory activities associated with planning, authoring, compiling and submitting highest-quality regulatory submissions to the FDA within company timelines and in...
Suggested
...therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
Summary
The Regulatory Data Manager will be a key member of the Global Regulatory Affairs (GRA) Process Excellence function, responsible for driving data...
Suggested
...therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
Summary
The Manager, Regulatory Affairs - Regulatory Project Management (RPM) provides planning and coordination supports for global and US regulatory activities...
Suggested
Work experience placement
...proactive global monitoring and surveillance of changes in the regulatory landscape focused on drug development lifecycle starting from... ...framework.
In this role, a typical day might include:
Project Management and leadership in the delivery of regulatory intelligence...
Suggested
Local area
Relocation package
Manager Global Regulatory Affairs
Princeton, New Jersey
EU GMP requirements
Must have Global Regulatory Affairs experience in the pharmaceutical or biotechnology industry.
Are you looking to make a career change to a stable company? This exciting opportunity offers a competitive...
Suggested
Work experience placement
...communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns, including... ...regulatory strategies for in-line products through life cycle management programs.
Contribute A&P expertise to the development of...
Suggested
Work experience placement
...The Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development...
Suggested
Local area
...Job Title: Regulatory Affairs Manager
Location: Princeton, NJ 08540
Duration: 6+ Months
Duties:
**Can be hybrid, but this role will be mostly onsite in Princeton, NJ. Local candidates.**
Supports regulatory affairs projects to organize, analyze,...
Suggested
Local area
Summary
This position reports to the VP, Global Regulatory Affairs. The incumbent responsible for supporting the development and implementation... ...to prepare, review and submit regulatory filing documents, manage documentation systems and maintain interactions with regulatory...
Suggested
Contract work
...many people as possible, to secure their right to good health. The way we work every day is important to us.
The Senior Manager, Regulatory Affairs will handle publishing and coordinating tasks for Global RA submission activities. Support the Global RA submission...
Suggested
Temporary work
Local area
Immediate start
Flexible hours
Management Expert
Contribute to the development of PSRs, when applicable, with the support of GSO or LSO
Track the actual implementation... ...policy
Maintain and update the local quality documents
PV Regulatory Intelligence
Ensure appropriate implementation and monitoring...
Suggested
Local area
Remote job
...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 America...
Suggested
Part time
Remote job
Worldwide
Flexible hours
...North America, we are headquartered in Princeton, NJ, with offices in California, Massachusetts, and Ontario.
Summary:
The Sr. Manager, Regulatory Affairs Compliance and Planning professional will lead or support regional and global projects by effectively delivering...
SUMMARY OF POSITION The Sr. Manager, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug development to all aspects of Our Client’s ’s drug development programs, policies and procedures; ensuring...
SUMMARY OF POSITION The Director, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations... ..., Regulatory Affairs and is based in Pine Brook, New Jersey. Manages team of 2-5 direct and indirect reports.
RESPONSIBILITIES...
...help along the way.
ROLE AND RESPONSIBILITIES:
~ Manage Lupin’s existing REMS programs and help in the development of new... ...~ Responsible for maintaining and updating various regulatory databases to ensure accuracy of information
~ Any additional...
Full time
...space (e.g.,
Houston, TX )
J&J Family of Companies
Director, Regulatory Affairs
in
Raritan ,
New Jersey
Director, Regulatory Affairs... ...strategies, PMR fulfillments, and other US-related issues. Manage routine maintenance submissions. Manage and track NA post-approval...
Holiday work
Full time
Temporary work
Remote job
