Clinical Research Coordinator // Lublin, PL

R&D Partners; Lublin; On-site; PLN 60,000 - 90,000; Full time

Job summary

R&D Partners is seeking a Clinical Research Coordinator to support clinical development activities within the healthcare sector. This on-site role is based in Lublin, Poland, and offers an opportunity to contribute to impactful studies while working closely with a dedicated clinical team.

You will manage data entry, query resolution, AE/SAE monitoring, and collaboration to ensure protocol compliance. The position requires attention to detail, teamwork, and the right to work in Poland.

Qualifications

• Experience in clinical research coordination or related roles.
• Strong attention to detail and organizational skills.
• Familiarity with data monitoring and verification processes.
• Ability to work independently and as part of a team.

Responsibilities

• Perform data entry and ensure accuracy in clinical trial documentation.
• Resolve queries and verify data, including source document uploads.
• Monitor and handle adverse events (AE) and serious adverse events (SAE).
• Collaborate with the clinical team to ensure compliance with study protocols.

Skills

Clinical research coordination

Attention to detail

Data monitoring

Teamwork/independence

Job description

Join a dynamic clinical research team where your attention to detail will directly contribute to the success of groundbreaking studies.

R&D Partners is seeking a Clinical Research Coordinator to support clinical development activities within the healthcare sector. This role is fully on-site in Lublin, PL, and offers an exciting opportunity to contribute to impactful research projects.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Perform data entry and ensure accuracy in clinical trial documentation.
• Resolve queries and verify data, including source document uploads.
• Monitor and handle adverse events (AE) and serious adverse events (SAE).
• Collaborate with the clinical team to ensure compliance with study protocols.

Key Skills and Requirements:

• Previous experience in clinical research coordination or related roles.
• Strong attention to detail and organizational skills.
• Familiarity with data monitoring and verification processes.
• Ability to work independently and as part of a team.

For more information, please contact Terrah-Leigh Pietersen.