Upvote
Downvote
Reg Affairs Sr Manager (Client Dedicated)
Share Job
- Suggest Revision
- With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
- Provides matrix/project leadership, training and guidance to junior team members.
- Advanced understanding of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization, licensing, lifecycle management; expert knowledge of ICH and other global regulatory guidelines; in-depth understanding of a regulatory speciality areas, such as preclinical, clinical, CMC, publishing, etc.
- Exceptional attention to detail and quality as well as outstanding editorial/proofreading skills
- At PPD Clinical Research Services we hire the best, develop ourselves and each other, and recognise the power of being one team.
Expired 14 days agoInactive Job
Similar Job
Relevance
Active