Req ID:

R010768

Locations:

Mississauga, ON, CA; Cambridge, Cambridgeshire, UK; London, UK; Carlsbad, CA; Palo Alto, CA; Philadelphia, PA -- [Remote/Home-Based]

Category:

Research & Development

Brief Description: The Associate Director, Medical Writing, is responsible for the efficient preparation of high-quality, strategically aligned medical writing deliverables within one or more program. S/he will work directly with cross functional teams to author regulatory documents (eg, protocols, clinical study reports, briefing books, submission documents, investigator brochures). For programs …

Req ID:

R010549

Locations:

Cambridge, Cambridgeshire, UK; London, UK; Philadelphia, PA -- [Remote/Home-Based]

Category:

Research & Development

Brief Description The Business & Technology Capabilities (B&TC) Sr. Analyst works closely with B&TC and GCDO colleagues, in collaboration with Information Services (IS) to support cross functional clinical study teams regarding the implementation and management of digital systems/technology used by GCDO including but not limited to Veeva Clinical Vault. The …

Req ID:

R010805

Locations:

London, UK; Philadelphia, PA -- [Remote/Home-Based]

Category:

Research & Development

The Director, Clinical Trial Feasibility & Site Intelligence is responsible for developing and overseeing strategic feasibility and site intelligence processes to inform clinical trial planning and provide clinical trial sites across the Jazz clinical trial portfolio. The role is responsible for process and resources that leverage cross functional expertise, analytics …

Req ID:

R010806

Locations:

London, UK; Philadelphia, PA -- [Remote/Home-Based]

Category:

Research & Development

Brief Description: The Director, Clinical Trial Start-Up is responsible for the strategic leadership and operational oversight of the Study Start-Up (SSU) process and staff. This role directs SSU planning, the development and optimization of end-to-end SSU processes and oversees the performance and development of SSU staff across multiple clinical programs. …

Req ID:

R010790

Locations:

London, UK; Philadelphia, PA -- [Remote/Home-Based]

Category:

Research & Development

Brief Description: The Senior Manager, Clinical Trial Study Start-Up is a subject matter expert in clinical study start-up and is responsible for leading process that enables planning, coordination, and execution of study, country and site-level start-up activities from site identification through to site activation. This role combines operational leadership with …

Req ID:

R010824

Locations:

Boston, MA; Trenton, NJ; Albany, NY; Philadelphia, PA -- [Remote/Home-Based]

Category:

Research & Development

Summary The Manager, Regulatory Affairs Global CMC will be responsible for CMC regulatory support of commercial/development projects worldwide. Essential Functions Ensure continued regulatory compliance of products though adherence to the change control procedures and completion of regulatory impact assessments. Coordinate with other team members to manage regulatory assessments for changes …