Senior Clinical Trail Associate, Associé principal aux essais cliniques, Accra, IQVIA

Senior Clinical Trail Associate, Associé principal aux essais cliniques, Accra, IQVIA

Role Responsibilities/ Responsabilités du rôle

16260-Sr Clin Trials Asst


Primary Location: Accra, Ghana

Full time



IQVIA is looking for a Senior Clinical Trail Associate based in Ghana that needs to be conversant in French.

Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.

Essential Functions

  • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
  • Collaborate with clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
  • Assist with periodic review of study files and completeness.
  • Collaborate with CRAs and RSU on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
  • Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
  • Act as a mentor for less experienced Clinical Trial Assistants (CTAs).
  • Assist with training and onboarding of new CTAs.
  • May serve as subject matter expert for business processes.
  • May lead CTA study teams.
  • May assist with interviewing and screening of potential new team members
  • May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
  • May participate in departmental quality or process improvement initiatives.


  • High School Diploma or equivalent Req
  • 5 administrative support experience.
  • Equivalent combination of education, training and experience.
  • Minimum two years clinical research experience strongly preferred.
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
  • Effective written and verbal communication skills including good command of English language.
  • Effective time management and organizational skills.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  • Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
  • Knowledge of applicable protocol requirements as provided in company training.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at

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