CRA II/Senior CRA

Warman O'Brien; Poland; Remote; PLN 60,000 - 90,000; Full time

Benefits offered by this job

competitive salary

company car or car allowance

one-month onboarding programme

Job summary

Warman O'Brien is seeking Clinical Research Associates at CRA II and Senior CRA levels to join a growing global biopharmaceutical team. This is a remote regional role in Poland with a focus on monitoring across sites.

Candidates based in Poznań, Bydgoszcz, Łódź, Wrocław and Szczecin are preferred; travel is required with 8–10 monitoring days per month and about 70% of sites within 250 km of home. Up to five protocols may be managed.

Qualifications

• Bachelor’s degree in life sciences or related field.
• 1 year of independent monitoring experience preferred for CRA I/II.
• 3+ years CRA experience preferred for Senior CRA.
• Fluent Polish and advanced English.
• Valid driving licence and willingness to travel.

Responsibilities

• Site qualification, initiation, routine monitoring and close-out visits.
• Source data review and query resolution.
• Documentation and collaboration with investigators and site teams.
• Ensure protocol compliance, patient safety and data integrity per ICH-GCP.

Skills

Independent working

Remote collaboration

Organisational skills

Communication skills

Problem solving

Travel willingness

Education

Bachelor's degree in Life Sciences

Job description

Clinical Research Associates (CRAII/Senior CRA) – Remote, Poland

We are seeking Clinical Research Associates at CRA II and Senior CRA levels to join a growing clinical research team within a global biopharmaceutical company (FSP model).

Candidates from across Poland are welcome to apply, with preference for those based in Poznań, Bydgoszcz, Łódź, Wrocław and Szczecin.

The Role

As a CRA, you will be responsible for clinical trial monitoring, ensuring protocol compliance, patient safety, data integrity and ICH-GCP standards. Responsibilities include site qualification, initiation, routine monitoring and close-out visits, source data review, query resolution, documentation and collaboration with investigators and site teams.

This is a remote regional role, with approximately 70% of sites within 250 km of your home and around 8–10 monitoring days per month, combining on‑site and remote visits. You may manage up to five protocols.

Requirements

• BA/BS/BSc in Life Sciences, Healthcare or a related field.
• At least 1 year of independent monitoring experience preferred for CRA I/II.
• 3+ years of CRA experience preferred for Senior CRA.
• Strong knowledge of clinical trials, ICH-GCP and applicable regulations.
• Fluent Polish and advanced English.
• Valid driving licence and willingness to travel.
• Strong organisational, communication and problem‑solving skills.
• Ability to work independently and collaboratively in a remote environment.

Experience in Cardiology, Haematology/Oncology, Inflammation, Metabolic Disorders, Neurology or Rare Diseases is advantageous but not essential.

What We Offer

• Remote-based working with a regional monitoring model.
• Structured one‑month onboarding programme covering systems, processes, study requirements and monitoring procedures.
• Ongoing support and development.
• Competitive salary and the choice of company car or car allowance.
• Opportunity to work across a range of clinical studies and therapeutic areas.

Preferred availability:

Candidates with a one-month notice period are particularly encouraged to apply.