Description
We are seeking a Senior CRA to collaborate with leading pharma companies and help patients worldwide.
As a Senior CRA at IQVIA, you will enjoy the stability and resources of a leading global contract research organization while gaining direct experience with one of our clients.
Responsibilities:
- Performing site selection, initiation, monitoring and close-out visits
- Supporting the development of a subject recruitment plan
- Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- Collaborating with experts at study sites and with client representatives
- Depending on client model, there might be remote-monitoring, involvement in study start-up processes, specialization on therapeutic area (pharmaceutical product or medical devices)
Qualifications:
- University Degree in life science or other scientific discipline or apprenticeship in health care
- Minimum of 3 years of on-site monitoring experience, alternatively an equivalent combination of education, training and experience
- Strong experience in monitoring of clinical trials
- Knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Strong written and verbal communication skills, attention to detail and ability to work in a fast-paced environment
- Good command of Polish and English language
- Flexibility to travel
What you can expect:
- Resources that promote your career growth
- Leaders that support flexible work schedules
- Programs to help you build your therapeutic knowledge
- Dynamic work environments that expose you to new experiences
- Home-office, company car, and more