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Clinical Study Coordinator

On-site Full-time

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Qualifications

To be successful in this role, candidates should possess the following qualifications:Strong background in life sciences, healthcare, or related fields. Excellent organizational and multitasking skills. Effective communication and interpersonal skills. Familiarity with Good Clinical Practice (GCP) and other regulatory guidelines. Ability to work collaboratively in a team environment.

About the job

We are seeking a dedicated and detail-oriented Clinical Study Coordinator to join our dynamic team. In this role, you will be responsible for overseeing the planning, execution, and management of clinical trials, ensuring compliance with regulatory requirements and adherence to study protocols. Your organizational skills will be pivotal in coordinating with various stakeholders, including investigators, participants, and regulatory bodies to facilitate the smooth conduct of clinical studies.

About Siloam Hospitals Group

Siloam Hospitals Group is a leading healthcare provider in Indonesia, dedicated to delivering high-quality medical services across our network of hospitals. Committed to excellence, we strive to improve the health and well-being of our communities through compassionate care, innovation, and advanced medical practices.

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