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.

Responsibilities:

  • 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.

Requirements:

  • 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:  joe.bell@lifesci-cm.com

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Consultant.

Joe Bell
Joe Bell
Delivery Consultant View Profile

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