Senior CRA: Lead Site Trials & Data Integrity

PowerToFly; Warszawa; On-site; PLN 120,000 - 180,000; Full time

Job summary

AbbVie is seeking an experienced Clinical Research Monitor to advance AbbVie's trials by partnering with study teams, investigators and site staff. You will drive site engagement, monitor performance, and ensure safety and data integrity across trials.

The role requires strong communication, regulatory knowledge and leadership to mentor junior CRAs and align on protocol execution and patient recruitment strategies.

Qualifications

• Appropriate tertiary qualification in health related disciplines (e.g., Medical, Scientific, Pharmacy, Nursing).
• Minimum of 3 years in clinical research monitoring of trials.
• Knowledge of ICH/GCP Guidelines and local regulatory requirements.

Responsibilities

• Serve as primary Sponsor contact for investigative sites and mentor monitoring staff.
• Aligns and trains site staff and investigators on trial goals and patient treatment principles.
• Conduct site evaluations, training, routine on-site/off-site monitoring and site closure with GMP/GCP compliance.
• Develop and apply site engagement strategies and report progress using engagement tools.
• Connect study protocol, scientific principles and trial requirements to day-to-day execution; support patient recruitment and protocol compliance.
• Mentor junior CRAs and assist in onboarding; participate in global/local task forces as needed.
• Monitor risk proactively with Central Monitoring to ensure patient safety and study performance.

Skills

Advanced communication skills

Excellent English

Cross-functional collaboration

Education

Appropriate tertiary qualification in health related disciplines

Clinical research monitoring experience (3+ years)

Job description

AbbVie is seeking an experienced Clinical Research Monitor to advance AbbVie's trials by partnering with study teams, investigators and site staff. You will drive site engagement, monitor performance, and ensure safety and data integrity across trials.

The role requires strong communication, regulatory knowledge and leadership to mentor junior CRAs and align on protocol execution and patient recruitment strategies.