CRA I: In-House Clinical Research (Remote-Ready)

Worldwide Clinical Trials; Warszawa; On-site; PLN 180,000 - 240,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Operations Site Manager to advance data quality and regulatory excellence across study sites. You will collaborate with cross-functional teams and oversee TMF submission activities to ensure compliance and timeliness.

In this role, you will drive site feasibility activities, identify suitable investigative sites, and support sponsors with operational oversight while working with a global team in a dynamic CRO environment.

Qualifications

• Four-year college curriculum with a life science focus, preferred.
• Two-year college curriculum or equivalent with relevant clinical research experience.
• Proficiency in English, Romanian and one other language (Polish highlighted)

Responsibilities

• Ensure quality and timely submission of data from study sites with proper safety reporting.
• Compile regulatory documents and ethical submission materials (IRB, consent, lab certs).
• Provide updates for site documentation in the Trial Master File (TMF).
• Conduct feasibility studies and site identification for potential sites.

Skills

Interpersonal skills

Remote collaboration

Customer focus

MS Office

CTMS

EDC Systems

Education

Four-year life science degree

Two-year college or equivalent with clinical research exposure

Tools

CTMS

EDC Systems

Job description

Worldwide Clinical Trials is seeking a Clinical Operations Site Manager to advance data quality and regulatory excellence across study sites. You will collaborate with cross-functional teams and oversee TMF submission activities to ensure compliance and timeliness.

In this role, you will drive site feasibility activities, identify suitable investigative sites, and support sponsors with operational oversight while working with a global team in a dynamic CRO environment.