Associate Director, Clinical Development

A Clinical Development Associate Director job is available through Adecco Medical and Science. This is a remote position requiring you to travel to New Jersey and California as needed. You must have a Bachelor’s degree with relevant work experience in Clinical Research, Allied Health, Project management or related field. You will be responsible for leading internal and outsourced site management and monitoring personnel and activities in support of clinical research studies.

Associate Director job responsibilities include:

Facilitating and maintaining the protocol risk assessment and characterization (PRAC), oversight and approval of protocols.
Contribute to the protocol, case report form and edit specifications, site profile, site feasibility questionnaire and recruitment plan.
Management and oversight of site monitoring deliverables and interfacing with CTTs on all aspects of study execution.
Provides leadership and content expertise for site management and monitoring activities from study start up through the study closeout stages of clinical studies to effectively oversee resources, timelines, quality and data delivery supporting database lock activities such as site selection/ activation, recruitment, protocol compliance and action item resolution.
Participate in the vendor selection process and managing vendors (e.g. CROs, FSPs, Technology Providers, etc.) in collaboration with the CTT.


Bachelor’s Degree with relevant work experience in Clinical Research, Allied Health, Project Management or related life science field.
Significant clinical research experience within a site management operations & monitoring leadership role in the pharmaceutical/device industry or CRO (preferably within a medium/ large CRO).
Advanced knowledge of research and development, clinical trials execution, and understanding of regulatory requirements/guidelines (e.g. ICH, GCP, safety reporting).
Advanced knowledge and understanding of project management guidelines & related concepts including experience managing large global projects.
Knowledge of global standards related to site management and monitoring activities.
Ability to travel overnight up to 30% of time. Must be able to maintain the necessary travel documents (e.g. valid driver’s license, passport, visa)

If you are interested in this Clinical Development Associate Director then please click APPLY NOW. For other opportunities available at Adecco Medical and Science go to If you have questions about the position or would like more information please contact Kayla Hanscom at (858) 812-2600 or by email at
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Reference number US_EN_2_108175_331385