×
Register Here to Apply for Jobs or Post Jobs. X

Associate Director, Clinical Trials

Job in Cambridge, Middlesex County, Massachusetts, 02140, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-02-01
Job specializations:
  • Healthcare
    Healthcare Management, Healthcare Administration
Salary/Wage Range or Industry Benchmark: 120000 - 150000 USD Yearly USD 120000.00 150000.00 YEAR
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
Qualifications
  • 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
#J-18808-Ljbffr
Position Requirements
10+ Years work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary