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...
10d
| 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...
10d
| Job Type | Full Time |
Senior Director, Pharmacovigilance
Cambridge, Massachusetts
The Senior Director, Pharmacovigilance will report to the Vice President, Head of Global Safety & Pharmacovigilance and will be responsible for supporting the Development organization as a PV expert and providing strategic and operational P...
10d
| Job Type | Full Time |
Director of Regulatory Affairs CMC
Cambridge, Massachusetts
Who is BlueRock? BlueRock Therapeutics, a wholly-owned and independently operated subsidiary of Bayer AG, is a leading engineered cell therapy company using its unique cell+gene platform to direct cellular differentiation and genetically en...
10d
| Job Type | Full Time |
Senior Director of Regulatory Affairs
New York, New York
Senior Director of Regulatory Affairs Job Ref: 112166 Category: Professional Department: OFFICE CORPORATE COMPLIANCE Location: 50 Water Street, 7th Floor, New York, NY 10004 Job Type: Regular Employment Type: Full-Time Hire In Rate: $190,00...
10d
| Job Type | Full Time |
CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP (Remote US or Canada)
New York, New York
Parexel International Corporation
The CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP provides strategic regulatory guidance to cross-functional project teams responsible for product development and post marketing commitments. The CMC Drug & Device expe...
10d
| Job Type | Full Time |
CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP (Remote US or Canada)
Phoenix, Arizona
Parexel International Corporation
The CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP provides strategic regulatory guidance to cross-functional project teams responsible for product development and post marketing commitments. The CMC Drug & Device expe...
10d
| Job Type | Full Time |
CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP (Remote US or Canada)
Houston, Texas
Parexel International Corporation
The CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP provides strategic regulatory guidance to cross-functional project teams responsible for product development and post marketing commitments. The CMC Drug & Device expe...
10d
| Job Type | Full Time |
CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP (Remote US or Canada)
Horsham, Pennsylvania
Parexel International Corporation
The CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP provides strategic regulatory guidance to cross-functional project teams responsible for product development and post marketing commitments. The CMC Drug & Device expe...
10d
| Job Type | Full Time |
CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP (Remote US or Canada)
Providence, Rhode Island
Parexel International Corporation
The CMC Drug & Device expert - Senior Regulatory Affairs Consultant, FSP provides strategic regulatory guidance to cross-functional project teams responsible for product development and post marketing commitments. The CMC Drug & Device expe...
10d
| Job Type | Full Time |