Job Summary:
EPM Scientific partner a Mid-Sized CRO in Oncology is seeking a Freelance Clinical Research Associate to support clinical operations team.
Main Responsibilities:
* Conduct site monitoring visits ensuring compliance with protocol GCP and regulatory requirements.
* Serve as primary point of contact for investigator sites ensuring high-quality data collection and patient safety.
* Support site selection feasibility assessments and start-up activities.
* Collaborate with cross-functional teams including Site Relationship Managers Project Managers and Medical Monitors.
* Identify and resolve site-level issues escalating risks as needed to ensure timely trial delivery.
* Maintain accurate and timely documentation of monitoring activities and site communications.
* Contribute to continuous process improvement and best practices in clinical operations.
Requirements:
* Bachelor's or Master's degree in Life Sciences or related field preferred.
* Strong experience as a CRA preferably 3-5 years.
* Strong understanding of ICH GCP and clinical trial processes.
* Experience in Oncology clinical trials highly preferred.
* Excellent organizational communication and interpersonal skills.
* Ability to work independently and manage multiple sites in Portugal.
* Willingness to travel up to 60% regionally.