Clinical Research Coordinator (Medan)

Join Siloam Hospitals Group as a Clinical Research Coordinator in Medan and play a pivotal role in advancing medical research and healthcare innovation. This position offers a unique opportunity to contribute to impactful clinical studies while working in a dynamic and supportive environment. As a Clinical Research Coordinator, you will be responsible for managing the day-to-day operations of clinical trials, ensuring compliance with regulatory standards, and collaborating with cross-functional teams to achieve study objectives.

Siloam Hospitals Group is a leading healthcare provider in Indonesia, known for its commitment to excellence and innovation. With a strong presence in Medan, we are dedicated to delivering high-quality care and advancing medical research. This role is perfect for professionals who are passionate about clinical research and want to make a difference in the healthcare industry.

In this role, you will handle various aspects of clinical trials, including patient recruitment, data collection, and study monitoring. You will work closely with clinical research associates, data managers, and other stakeholders to ensure the smooth execution of studies. This position offers competitive compensation, professional development opportunities, and a collaborative work environment.

📋 Tanggung Jawab Pekerjaan

• Manage the day-to-day operations of clinical trials, ensuring compliance with regulatory standards such as ICMJE and ICH-GCP.
• Recruit and screen potential study participants, coordinating with healthcare providers and patient advocacy groups.
• Collect and manage clinical data, ensuring accuracy and completeness using tools like REDCap and Clinical Data Management Systems.
• Monitor study progress, identifying and resolving any issues that may arise.
• Collaborate with cross-functional teams, including clinical research associates, data managers, and investigators, to achieve study objectives.
• Prepare and submit regulatory documents, such as Informed Consent Forms and Case Report Forms, ensuring adherence to legal and ethical standards.
• Conduct site visits and audits to ensure compliance with study protocols and regulatory requirements.
• Maintain accurate and up-to-date documentation of all study activities.

🎓 Kualifikasi & Syarat

• Bachelor's degree in Life Sciences, Medicine, Nursing, or a related field.
• Minimum of 3 years of experience in clinical research coordination or a related role.
• Certification in Good Clinical Practice (GCP) or equivalent experience.
• Proficient in using clinical research software and tools, such as REDCap, Clinical Data Management Systems, and electronic data capture systems.
• Strong understanding of regulatory requirements and ethical considerations in clinical research.
• Excellent communication and interpersonal skills, with the ability to work effectively with diverse teams.
• Attention to detail and the ability to manage multiple tasks in a fast-paced environment.
• Fluency in both English and Indonesian languages.

🛠️ Keahlian

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