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Associate Director, Clinical Trials
Job in
Cambridge, Middlesex County, Massachusetts, 02140, USA
Listed on 2026-02-01
Listing for:
Scorpion Therapeutics
Full Time
position Listed on 2026-02-01
Job specializations:
-
Healthcare
Healthcare Management, Healthcare Administration
Job Description & How to Apply Below
Role Summary
As Associate Director Clinical Trials you are responsible for the execution of clinical trials, mainly with regard to operational and administrative aspects. This implies the preparation and processing of national and international projects under consideration of the local laws, international guidelines (ICH GCP) and applicable SOPs. You perform activities related with the heading of a project team, the supervision/ control of third-party providers, the timely performance of all services, as well as the problem management by interacting with all departments involved.
Responsibilities- Leads 1 or more complex/large scale clinical trial/s in either early or late stage clinical development within a program (+8 years of experience)
- Leading communications, issue escalations and helping the teams within the program to further develop
- May have more junior trial managers reporting. Global study management experience needed
- Manages the Clinical Research Organization (CRO) and vendor(s) as it relates to clinical program level deliverables
- Manages clinical study timelines for the program(s)
- Ensures inspection readiness throughout the clinical program lifecycle
- May be responsible for line management of one or more direct report
- A Bachelor’s degree in the life sciences or a university degree in a related field with experience in the health industry. Advanced degree preferred
- Minimum 8 years of experience in pharmaceutical/biotech or related industry with at least 4 years’ experience in Global Clinical Development working on cross-functional teams
- Knowledge and experience working with legislation and international guidelines (ICH-GCP/CFR) for the performance of clinical research projects
- Demonstrated experience with addressing regulatory inspections or internal process audits and drafting/reviewing responses to Health Authority and Ethics committee questions
- PMP or equivalent certification desirable
- Good communication and presentation skills both written and spoken inclusive of confident, articulate, and professional speaking abilities (with some experience)
- Able to communicate strategy and decisions across different functions
Position Requirements
10+ Years
work experience
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