LAVORO REGULATORY AFFAIRS CLINICAL TRIALS

Prepares and/or reviews regulatory documents to support clinical trial submissions... independently provides regulatory support for complex projects and programs...

Member of relevant clinical sub teams (cst), clinical trial teams (ctt) and an ad hoc attendee at product development team (pdt) meetings active collaboration with...

Primary responsibility of a regulatory affairs specialist is to prepare and submit regulatory documents for product approval... additionally, regulatory affairs...

Primary responsibility of a regulatory affairs manager is to prepare and submit regulatory documents for product approval... additionally, regulatory affairs manager...

They are looking for a clinical affairs program manager europe... additional responsibilities include management of clinical trials approvals with local irbs and/or...

Provides regulatory affairs support during internal and external audits... assists in the development of standard methodologies for regulatory affairs processes...

Collaborate with global regulatory teams and the global regulatory affairs (gra) function/teams to facilitate regulatory activities... the associate director, regulatory...

As a subject matter authority for regulatory affairs the individual will provide guidance to local and global business partners... the regulatory affairs associate...

Experience required minimum of 7 years experience in regulatory affairs... ensure effective communication within global regulatory affairs (gra), cross-functional...

Meditrial is a full-service clinical research organization (cro) dedicated to clinical trial conduct, medical education, regulatory affairs, and market access...

Direct interfaces with regulatory authorities as needed on issues... demonstrated ability to develop and implement regulatory strategies, facilitate approvals, resolve...

regulatory affairs manager - uxbridge - 12-month contract    our client, a globally recognised pioneer in biotechnology, are recruiting for the position of regulatory...

Experience required at least 5-7 years’ experience in regulatory affairs... lead regulatory subteam to ensure nda/bla/maa/extensions/variations filings meet project...

Giorni fa talent solutions, part of manpower group, for an important pharmaceutical client based in florence, is currently recruiting a global regulatory affairs...

Main activities the clinical operations trainee will support the operational activities and execution of global medical affairs air generated data, as part of the...

Experience required at least 5-7 years’ experience in regulatory affairs... technical skills emerging understanding of clinical development of drugs and/or novel...

Essential functions • acts as a regulatory team leader on more complex projects, which may include technical writing; • prepares and\/or reviews regulatory documentation...

Ensures that regulatory submission timelines are aligned with program level and company objectives...   experience required at least 5-7 years’ experience in regulatory...

Talent solutions, part of manpower group, for an important pharmaceutical client based in florence, is currently recruiting a motivated regulatory affairs associate...