EPM Scientific are currently partnered with a Mid-Sized CRO running a global project in Oncology.
They are urgently seeking a Freelance Clinical Research Associate (CRA) to support their expanding clinical operations team.
See a short summary below: Contract Conditions: Start date: ASAP Location: Portugal, Remote Contract Type: Freelance / Consultant - 0.4-0.5 FTE, 12 Months Contract (36 Month Project) Language: English, Portuguese Project: Oncology Key Responsibilities: Conduct site monitoring visits (pre-study, initiation, routine, and close-out) to ensure compliance with protocol, GCP, and regulatory requirements.
Serve as the 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 (3-5 years of experience preferred) as a CRA.
Strong understanding of ICH GCP, and clinical trial processes.
Experience in Oncology clinical trials is 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.
If this role is of interest to you, please apply directly to learn more.
If not, feel free to share with your network.
