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Clinical Trial Manager
hace 2 meses
The Clinical Trial Manager is a key member of our team, responsible for delivering all clinical aspects of our studies. This role requires a high level of expertise and attention to detail, ensuring that our clinical trials are conducted to the highest standards.
Key Responsibilities- Oversee the clinical portion of the study budget and develop monitoring plans and tools.
- Train and manage Clinical Research Associates (CRAs) to ensure they have the necessary skills and knowledge to conduct clinical trials.
- Drive enrolment and study start-up activities, and review trip reports to ensure compliance with regulatory requirements.
- Implement corrective and preventative action plans to mitigate risks and ensure the success of our clinical trials.
- Liaise with sponsors, vendors, and cross-functional teams to ensure seamless communication and collaboration.
- Provide regular reporting and metrics on all clinical activities to stakeholders.
- 4-year degree or equivalent combination of education and experience.
- Demonstrated ability to drive clinical deliverables of a study.
- Subject matter expertise in the designated therapeutic area.
- Prior monitoring experience is preferred.
- Ability to travel up to 20%.
- Fluent in local language - both written and verbal.
At ICON Plc, we offer a competitive salary package, annual bonuses, and a range of health-related benefits to employees and their families. We also provide competitive retirement plans and related benefits such as life assurance. Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family.
We are an equal opportunity and inclusive employer, committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
