Regulatory affairs associate jobs in Boston, MA
Clinical Project Associate
As Clinical Project Associate, you will be accountable for providing clinical trial coordination support, along with implementing operational plans in accordance with regulatory guidelines and..
Clinical Trial Associate
Description. The Clinical Trial Associate (CTA) supports the Clinical Operations, Supply and Data.. Collect, file, and track clinical trial associated study and regulatory documents for the Trial Master..
Associate Director, Regulatory Affairs
Associate Director, Regulatory Affairs. Boston, MA. Permanent Proclinical is seeking a strategic.. Experience in oncology or rare disease. The Associate Director will. Develop and execute innovative..
Associate Director, Regulatory Affairs
Associate Director, Regulatory Affairs. Boston, MA. Permanent Proclinical is seeking a strategic.. Experience in oncology or rare disease. The Associate Director will. Develop and execute innovative..
Associate Director, Regulatory Affairs CMC
Reporting to the Senior Director of Regulatory Affairs CMC, you will work closely with cross functional.. As the Regulatory CMC lead for these programs, you will have the opportunity to devise and implement..
Manager, Regulatory Affairs
Job Description The Manager, Regulatory Affairs provides regulatory support for oncology products in.. and late stage development. In this role, the Manager of Regulatory Affairs will support the regulatory..
Assurance Associate
Vaco Boston has partnered with our client, a rapidly growing CPA firm in the Boston area, that is seeking to hire an Assurance Associate to join their team. This individual will be responsible..
Regulatory Affairs Director
Job Description About the Job The Regulatory Affairs (RA) Director is responsible for the development.. This role is responsible for international regulatory strategy, including registration of new products..
Mgr Regulatory Affairs
Mgr Regulatory Affairs. req1193. OVERVIEW. Responsible for pre market and post market activities as.. Provide input and assist in determining the appropriate regulatory strategies for product clearance..
Manager, Regulatory Affairs
Reporting to the Sr. Director, Regulatory Affairs, the right experienced candidate will be a.. advanced degree preferred.At least 5 years pharmaceutical industry regulatory experienceExperience in US..