Reference: 316 22/06/2022 17:16:42

Clinical Trial Contract Specialist.

Buenos Aires - Argentina Competitive

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Clinical Trial Contract Specialist to join our Clinical Operations team. This position plays a key role in the study start-up and clinical trial management processes. The Contract Specialist will play a key role in advancing the start-up of our projects. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.


  • Is responsible for preparing, negotiating, tracking and finalizing the Confidentiality Agreements (CDA), Clinical Trial Agreements (CTA), Budgets and Letters of Indemnification (LOI) as well as Amendments to these documents, as needed.
  • Negotiates final CDA and CTA templates with clients, and the internal project team.
  • Manages all required contractual agreements with investigator sites. This includes distribution, negotiation of budget and language, tracking and finalization.
  • Proactively identifies site contract related risks and potential roadblocks.
  • Prepares contract approval timelines with investigators and leads efforts to obtain contract approval to meet study deliverables.
  • Maintains communication with client, project team and sites regarding status of all contractual requirements.
  • Collaborates with the project team to ensure the client deliverables and expectations are achieved.
  • Liaises with internal customers to review contract or budget areas that impact final execution of site contracts.
  • Maintains tracking regarding site contracts and provides regular updates as agreed by the study team to the project team and client regarding status and efforts to ensure timelines are maintained.
  • Provides training on clinical site contractual requirements and negotiation.
  • Participates in corporate initiatives and actions that ensure the continued success of the company.


  • Bachelors degree in business administration, legal studies, or life sciences.
  • 1 year of CRO experience or investigator site experience negotiating site agreements.
  • Ability to work with internal and external customers/vendors to meet project-specific goals.
  • Ability to manage high volume work and meet rigorous deadlines.
  • Flexibility to strategically manage negotiations with minimal oversight.
  • Ability to interact with site, clients, and other functional areas as secondary project contact for contracting issues and questions.
  • Ability to manage time and project requirements based on study deliverables.
  • Fluency in English

We kindly ask to send applications in English.

If this position is of interest to you, Apply below or get in touch at:

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Joe Bell
Joe Bell
Delivery Consultant View Profile

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