Show Filters
Regulatory Affairs Consultant - CTA /EU-CTR
King of Prussia, Pennsylvania
Parexel International Corporation
Parexel Croatia is currently looking for an experienced Regulatory Affairs Consultant to provide operational and business clinical trials regulatory consultancy to clients, including new EU CTR regulations and to coordinate large and comple...
8h
| Job Type | Full Time |
Regulatory Affairs Professional - CTA
King of Prussia, Pennsylvania
Parexel International Corporation
We are recruiting for experienced Regulatory Affairs Professionals on various levels. In this role, you will focus on clinical trial submissions. We are looking for someone who is experienced in CTA, EU-CTR knowledge and experience would be...
8h
| Job Type | Full Time |
Senior Regulatory Affairs Consultant / Regulatory Project Lead
Billerica, Massachusetts
Parexel International Corporation
If you are passionate about innovative therapies, love leading complex regulatory filings, and live for quality, on time, and within budget project deliverables, Parexel is E-X-P-A-N-D-I-N-G and we currently have openings for Senior Regulat...
8h
| Job Type | Full Time |
(Senior) Regulatory Affairs Consultant /
King of Prussia, Pennsylvania
Parexel International Corporation
PMDAMHLW NDA 1. * NDA * USEU * * PMDAPMDAPMDA * NDACTDNDA * ODD 2. * * * * * * CRO10 * PMDAJNDACTD * PMDA * * * * Microsoft ExcelWordPower Point
8h
| Job Type | Full Time |
Vice President, Technical / Clinical Regulatory Affairs SME - Oncology
Billerica, Massachusetts
Parexel International Corporation
As one of our ex-FDA colleagues describes it: "you get to see a lot of cool stuff very quickly". If you're looking for the opportunity to influence the development strategies of pace-setting biopharma companies, there's no better place to b...
8h
| Job Type | Full Time |
King of Prussia, Pennsylvania
Parexel International Corporation
The Manager within R&A provides leadership and direction to Associates, Consultants and Senior Consultants, actively managing employee performance and development. Additionally acts as a role model and provides or organizes coaching/mentori...
8h
| Job Type | Full Time |
Director of Regulatory Affairs (Remote)
Lexington, Massachusetts
DIRECTOR OF REGULATORY AFFAIRS Partner Therapeutics is a commercial biopharmaceutical company committed to improving the lives of patients with cancer and other serious diseases. Our dedicated team brings a rigorous approach to science, est...
13h
| Job Type | Full Time |
Senior Manager, Process Sciences
Cambridge, Massachusetts
This role is considered On-Site. Overview This position will be a part of the CMC Drug Substance Process Sciences group, leading a small team. This role will include process development, in-house non-GMP manufacturing of siRNA and process t...
14h
| Job Type | Full Time |
Labeling Process Manager- Intagras
Syneos Health/ inVentiv Health Commercial LLC
Description Manager, Regulatory Consulting Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into...
15h
| Job Type | Full Time |
Director, Drug Product SME, CMC
Gaithersburg, Maryland
We go where others won't, taking on some of the biggest public health challenges to protect and enhance millions of lives, and create a better, more secure world.Here, you will join passionate professionals who advance their scientific, tec...
15h
| Job Type | Full Time |