Coordinate and ensure flawless execution of clinical trials, adherence to protocols, and regulatory requirements.Collaborate strictly with cross-functional teams to determine study objectives and successfully implement project plans.Monitor trial sites, ensuring compliance with study protocols, and document findings in detailed reports.Maintain accurate and timely data collection, verification, and entry to support outstanding research outcomes.Provide mentorship and guidance to junior CRAs, encouraging a collaborative and inclusive team environment.Required Qualifications
- Proven experience as a Clinical Research Associate (CRA) with a minimum of 2 years in a similar role.
- Bachelor's degree or equivalent experience in Life Sciences, Nursing, or a related field.
- In-depth knowledge of clinical research processes, regulations, and guidelines.
- Outstanding organizational skills and attention to detail.
- Strong communication and interpersonal skills to effectively collaborate with diverse teams and collaborators.
- Fluency in English, both written and spoken; proficiency in Polish is highly advantageous.
- Oncology experience
Why Join Us?
At Thermo Fisher Scientific, we give you the opportunity to contribute to groundbreaking research that improves the health, cleanliness, and safety of the world. Join us and be part of a company that is motivated by integrity, innovation, and intensity. Together, we can achieve outstanding results!