For one of our clients, a global health care company, we are looking for a Clinical Trial Agreements Consultant.
Job Description
In this role you will be responsible and accountable for the preparation, negotiation and finalisation/signature of clinical trial agreements and budgets.
Responsibilities
- You initiate and follow through on the process of getting Clinical Trial Agreements in place at the study sites.
- You act as the central point of contact for sites and study teams, ensuring alignment on the CTA contents and wording.
- You work with relevant stakeholders such as Legal, Quality, etc to ensure compliance with laws and client's policy.
- You negotiate with study sites, ensuring that the site budgets are in accordance with the protocol requirements and client's policies. In case of discrepancies, you escalate and seek approval as appropriate.
- You ensure clear communication to sites and study teams on status updates, timelines, issues, etc. You maintain a result-oriented approach in working on issue resolution while mindful of projected timelines.
Requirements
- Bachelor's or master's degree in Life Sciences or any other orientation with a first experience in clinical trials.
- Fluency in English.
- Proactive and result oriented mindset.
- Ability to multitask.
- Good communication skills.
Contract information
- Permanent contract with Oxford Global Resources.
- Location : Brussels
- Full-time.
