Freelance Clinical Research Associate
EPM Scientific are currently partnered with a small Contract Research Organisation supporting international clinical research programs across Oncology and Cardiology. They are seeking a Freelance Clinical Research Associate to support ongoing clinical studies in Latvia. This position will play a key role in ensuring clinical trial activities are conducted in accordance with study protocols, ICH-GCP guidelines, and applicable regulatory requirements. See a summary of the role below:
Role Overview:
- Start date: November 2026
- Location: Latvia
- Contract Type: Freelance / Consultant - 0.3 FTE Contract
- Language: Latvian and English
- Project: Oncology and Cardiology Clinical Studies
Key Responsibilities:
- Conduct site monitoring activities including site initiation, routine monitoring, and close-out visits.
- Ensure investigator sites remain compliant with study protocols, ICH-GCP guidelines, and local regulations.
- Perform source data verification (SDV) and review clinical trial documentation for accuracy and completeness.
- Develop and maintain strong working relationships with investigators and site staff.
- Track and resolve site issues, protocol deviations, and data queries in a timely manner.
- Collaborate with Clinical Operations, Project Management, and sponsor teams to support study delivery and timelines.
Requirements:
- Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related scientific discipline.
- Previous experience as a Clinical Research Associate monitoring clinical trials.
- Experience within Oncology and/or Cardiology studies is strongly preferred.
- Solid understanding of clinical trial processes, ICH-GCP, and regulatory requirements.
- Fluency in Latvian and English.
- Strong organisational skills with the ability to work independently in a freelance capacity.
- Excellent communication and stakeholder management skills.
If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.
FAQs
Congratulations, we understand that taking the time to apply is a big step. When you apply, your details go directly to the consultant who is sourcing talent. Due to demand, we may not get back to all applicants that have applied. However, we always keep your resume and details on file so when we see similar roles or see skillsets that drive growth in organizations, we will always reach out to discuss opportunities.
Yes. Even if this role isn’t a perfect match, applying allows us to understand your expertise and ambitions, ensuring you're on our radar for the right opportunity when it arises.
We also work in several ways, firstly we advertise our roles available on our site, however, often due to confidentiality we may not post all. We also work with clients who are more focused on skills and understanding what is required to future-proof their business.
That's why we recommend registering your resume so you can be considered for roles that have yet to be created.
Yes, we help with CV and interview preparation. From customized support on how to optimize your CV to interview preparation and compensation negotiations, we advocate for you throughout your next career move.