Clinical Trial Contract Specialist
hace 3 días
**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 area**s 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 mínimal 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
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