In-House Clinical Research Associate I (Remote)

Worldwide Clinical Trials; Warszawa; Hybrid; PLN 120,000 - 180,000; Full time

Job summary

Worldwide Clinical Trials seeks an experienced Clinical Operations Site Manager to join our global team in Warsaw. You will drive quality data submission, regulatory filing support, and TMF documentation across multiple studies.

You will collaborate with cross‑functional colleagues in a supportive, remote-inclusive environment, using CTMS, EDC and MS Office to ensure study success and patient safety across therapeutic areas.

Qualifications

• Four-year college curriculum in life sciences preferred.
• One year experience in clinical research or related field.
• Proficiency in English and one additional language is a plus.
• Ability to work effectively in a team and communicate with sponsors.

Responsibilities

• Ensure high-quality data from study sites and timely reporting for safety events.
• Compile regulatory documents and ethical submissions (IRB, informed consent, lab certification).
• Update TMF with site-related documentation for filing.
• Perform feasibility studies/site identification for potential sites.

Skills

Communication skills

Remote collaboration

Customer focus

MS Office / CTMS / EDC

Education

Bachelor's degree in life sciences

1 year clinical research experience

Tools

MS Office

CTMS

EDC Systems

Job description

Worldwide Clinical Trials seeks an experienced Clinical Operations Site Manager to join our global team in Warsaw. You will drive quality data submission, regulatory filing support, and TMF documentation across multiple studies.

You will collaborate with cross‑functional colleagues in a supportive, remote-inclusive environment, using CTMS, EDC and MS Office to ensure study success and patient safety across therapeutic areas.