job description
Join Equilab International, a leading global clinical research organization, as a Clinical Research Associate (CRA) in the vibrant and culturally rich island of Bali, Indonesia. This is an exceptional opportunity to advance your career in clinical research while enjoying the unique lifestyle and professional growth opportunities in one of the worldās most sought-after destinations.
As a CRA, you will play a pivotal role in ensuring the successful conduct of clinical trials, adhering to Good Clinical Practice (GCP), regulatory standards, and study protocols. You will collaborate with cross-functional teams, including investigators, site staff, and sponsors, to monitor trial progress, ensure data integrity, and maintain compliance with ethical and regulatory requirements. This role offers a dynamic work environment where your expertise will directly contribute to the development of life-changing medical treatments and therapies.
Baliās growing reputation as a hub for healthcare and research innovation makes it an ideal location for this role. Whether you are based in Canggu, Ubud, Denpasar, Jimbaran, Nusa Dua, Kuta, or Badung, you will have the opportunity to work in a supportive and collaborative environment while enjoying the islandās natural beauty, rich culture, and modern amenities. Equilab International is committed to fostering professional development, offering competitive compensation, and providing a work-life balance that allows you to thrive both personally and professionally.
If you are a detail-oriented, proactive, and passionate clinical research professional, we invite you to apply and become part of our mission to advance healthcare through innovative research.
Responsibility
- Monitor clinical trial sites to ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
- Conduct site initiation, interim monitoring, and close-out visits to verify data accuracy and protocol adherence.
- Collaborate with investigators, site staff, and sponsors to address any issues or deviations during the trial.
- Review and verify source documents, case report forms (CRFs), and electronic data capture (EDC) systems for completeness and accuracy.
- Prepare and submit monitoring visit reports, ensuring timely and accurate documentation of findings and action items.
- Facilitate communication between study sites and sponsors, providing updates on trial progress and resolving any operational challenges.
- Ensure proper storage, handling, and accountability of investigational products and study materials.
- Participate in study team meetings, contributing insights and recommendations to optimize trial execution.
Qualifications
- Bachelorās degree in Life Sciences, Pharmacy, Nursing, or a related field (Masterās degree preferred).
- Minimum of 2 years of experience as a Clinical Research Associate (CRA) or in a similar role within clinical research.
- Strong knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
- Experience with site monitoring, data verification, and regulatory compliance in clinical trials.
- Excellent communication, organizational, and problem-solving skills, with the ability to work independently and as part of a team.
- Proficiency in English (written and verbal) is required; additional languages are a plus.
- Willingness to travel frequently to clinical trial sites across Bali and other regions in Indonesia.
- Detail-oriented, proactive, and able to manage multiple priorities in a fast-paced environment.