Job DescriptionABOUT US:
At Vitrafy Life Sciences, we’re not just part of the biotech industry, we’re redefining it by improving the quality of healthcare treatments by providing effective cryopr...
Job DescriptionAbout Slate
Slate Medicines is a clinical-stage biotechnology company committed to advancing innovative new therapies that may broaden the treatment paradigm and potentially improve out...
Job DescriptionPosition Overview
The Quality & Regulatory Affairs Manager is responsible for ensuring organizational compliance with applicable regulatory requirements while leading and improving ...
Job DescriptionPosition Summary
Our Startup Client is seeking an experienced Vice President of Quality & Regulatory Affairs to lead the Quality and Regulatory functions for a clinical-stage biotec...
Job DescriptionCompany Description
Mazza Healthcare is a healthcare solutions company with strong expertise in global sourcing and private label portfolio development. We advance the cost-effectivenes...
Job DescriptionMCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Toge...
Job DescriptionVice President, Regulatory Affairs
Position Overview
The Vice President, Regulatory Affairs will provide strategic and operational leadership for the Regulatory Affairs function suppo...
Job Description
About the Company
Breckenridge Pharmaceutical develops and markets high-quality, added-value and cost-effective generic drugs in the United States. Our products are developed in the gr...
Job DescriptionRegulatory Affairs Specialist
Job Type: Full time - Permanent
Location: Madison, New Jersey (On-site)
A commercial-stage transplant technology company, part of a global medtech group, ...
Job DescriptionWe’re Hiring: Regulatory Affairs & Compliance Manager
? Indianapolis, IN | ? $90,000–$95,000
Kelly Science & Clinical is seeking a Regulatory Affairs & Compliance Manag...
Job DescriptionThe group exists to provide professional consulting, implementation and project management services to clients to enable the conduct of clinical trials and associated regulatory activit...
Job DescriptionQMS Consulting seeks a Regulatory Specialist with direct experience drafting federal rules for the
a federal agriculture agency. The specialist will serve as a rulemaking subject matter...
Job DescriptionSenior Director, Regulatory Affairs - Hybrid NYC Area
Key Responsibilities
Develop and execute regulatory strategies supporting clinical development and future product approvals.
Le...
Job DescriptionRetained Search | Hybrid Position
I am conducting a retained search for a Vice President, Global Regulatory & Clinical Strategy on behalf of a commercial-stage biotech with a growi...
Job DescriptionSenior Director, Regulatory Affairs (fully on-site in San Diego)
Summary
Our client is a well-funded, growth-stage medical technology company developing a Class III active implantable ...
Job DescriptionResponsibilities
Maintain regulatory binders and essential documents for active oncology trials after study activation
Prepare and submit IRB continuing reviews, amendments, safety r...