Performs assigned activities within the country that lead to start-up of investigative sites in all phases of clinical trials. Responsible for providing delivery and expertise in one or more of the following functional areas: investigator site contracts, ethics and regulatory submissions, and review and finalization of essential documents required for site initiation.
PPD is seeking a Sr. Manager/Associate Director to join their growing Global Regulatory Affairs (GRA) Department in Cambridge.
In this role, you will provide innovative solutions including global regulatory therapeutic area expertise and client interface to provide strategic regulatory intelligence, guidance and regulatory expertise for product development from preclinical through registration and product optimization.
Urgent: Regulatory Affairs Manager/Regulatory Affairs Lead: This is an exciting opportunity to join a large and growing Medical Device company in the New York/New Jersey area. You will be managing a talented team working on a range of strong products already on the market with a friendly and fast paced office.
Regulatory Affairs Snr Manager / French speaking Switzerland / Global CMC Biotech role.
My Client is a Global organization that develops, manufactures and markets products that save and sustain the lives of people. They have a varied product portfolio which includes pharmaceutical and biotechnology products. Their office in Switzerland is seeking a highly skilled CMC regulatory specialist to operate in a unique role. Contact me, Theo Moore , on +44 (0)207 801 3384.
If you have over 7 years Regulatory CMC experience for development and MAA activities and are looking for a great next challenge, then this could be the role for you… In the short term you will be leading CMC regulatory teams to develop global CMC regulatory strategy...In the long term you will grow to lead and manage your own team whilst gaining biotech experience. Call Theo Moore or Matt Greig on +44 (0)207 801 3380 or email your CV to CV@advregulatory.com
Our client is actively seeking a Regulatory Affairs/ Quality Assurance Specialist to join their global medical devices operation in Germany.
Our client is a global medical devices company with products and services available in over 100 countries around the world.
Exciting opportunity to join one of the largest Global CROs in their Global Start-Up Team. This is a full-time, permanent position.
This is a home-based position.
This role is for someone with healthy experience in Clinical Research who has a strong interest in Local and EU submissions. You will have an experienced background in Regulatory Affairs, Clinical Research or Study Start-Up. Candidates must have experience with Global Strategy.
Opportunity to join one of the largest Global CROs in their Start-Up Team. This is a full-time, contract position for 6 months, with strong possibility of extension. You can be based on-site in the office or be home-based. This role is for someone with healthy experience in Clinical Research who has a strong interest in Global submissions. You will have an experienced background in Regulatory Affairs, Clinical Research or Study Start-Up. Candidates must have experience with Glob
Study Start-up/Regulatory/Clinical Start-up *MANAGER* - Leuven, Belgium – Ambitious midsized CRO - Join our growing organisation and lead our EU regulatory team in the creation and development of regulatory documents and strategies.
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