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Lead Clinical Trials Specialist
2 semanas atrás
Responsible for the day-to-day management of one or more clinical trials in assigned countries, ensuring compliance with regulations and good clinical practice.
- Collaborate on study country prospects
- Conduct feasibility assessments for assigned studies, including country and centre feasibility evaluation
- Manage local/regional assigned studies
- Plan, manage, and oversee clinical trials activities such as administrative, budget, regulatory, logistics, contracts, training, and set-up
The ideal candidate will have excellent communication and organisational skills, with the ability to work effectively in a team environment. They will also be able to interpret and implement clinical trial protocols, and ensure that all relevant documentation is up-to-date and accurate.
Our company is committed to advancing therapeutic progress and improving patient outcomes. We offer a competitive salary and benefits package, as well as opportunities for professional development and growth.
As a Clinical Trial Project Coordinator, you will play a key role in our company's mission to improve patient lives through innovative research and development.
Key responsibilities include:
- Managing clinical trial data and documentation
- Coordinating with investigators and site staff
- Ensuring compliance with regulatory requirements
- Identifying and mitigating risks and issues
