CRA II

Warman O'Brien; Polska; Hybrid; PLN 67,000 - 100,000; Full time

Benefits offered by this job

Company car or car allowance

Structured onboarding programme

Ongoing support and development

Job summary

Warman O'Brien is seeking a Clinical Research Associate II to join a growing clinical research team within a global biopharmaceutical company (FSP model). This remote regional role in Poland offers 70% of sites within 250 km of your home and ~8-10 monitoring days per month, with potential to manage up to five protocols.

As CRA, you will monitor trials, ensure protocol compliance, patient safety and data integrity per ICH-GCP standards, performing site qualification, initiation, routine

Qualifications

• BA/BS/BSc in Life Sciences, Healthcare or a related field.
• At least 1 year of independent monitoring experience preferred for CRA I/II.
• Fluent Polish and advanced English.
• Valid driving licence and willingness to travel.

Responsibilities

• Monitor clinical trials and ensure protocol compliance.
• Perform site qualification, initiation, routine monitoring and close-out visits.
• Review source data and resolve queries to ensure data integrity.
• Collaborate with investigators and site teams to support study delivery.

Skills

Organisation

Communication

Problem solving

Remote collaboration

Education

Bachelor's degree in Life Sciences/Healthcare

Job description

We are seeking Clinical Research Associates at CRA II level 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.
• 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.