Freelance Clinical Research Associate Opportunity
Our client, a prominent CRO, is seeking a Freelance Clinical Research Associate to support their team on a global Oncology project. This role involves conducting site monitoring visits to ensure protocol, GCP, and regulatory compliance.
* The ideal candidate will serve as the primary point of contact for investigator sites to collect high-quality data and ensure patient safety.
* They will also support site selection, feasibility assessments, and start-up activities, collaborating with cross-functional teams to identify and resolve site-level issues.
Requirements:
A Bachelor's or Master's degree in Life Sciences or a related field is required, along with 3-5 years of experience as a CRA, preferably in Oncology clinical trials.
Key Skills:
* Strong organizational, communication, and interpersonal skills are essential for this role.
* The ideal candidate must be able to work independently and manage multiple sites in Portugal.
Travel Requirements:
Up to 60% regional travel is required for this position.