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 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.