Senior Clinical Research Associate (CRA) - Remote in Bali, Indonesia

Parexel International · 📍 Bali, Indonesia (Remote - Canggu, Ubud, Denpasar, Jimbaran, Nusa Dua, Kuta, Badung) · Diposting 2026-10-09
FULL_TIME⭐ TERVERIFIKASI
IDR 18000000 - 30000000
Parexel International is seeking a highly skilled and experienced Senior Clinical Research Associate (CRA) to join our team in Bali, Indonesia. This is a remote position, allowing you to work from the comfort of your home in one of Bali's beautiful locations. As a Senior CRA, you will play a crucial role in managing and overseeing clinical research studies, ensuring their successful completion and adherence to regulatory guidelines.

📋 Tanggung Jawab Pekerjaan

Manage and oversee the day-to-day activities of clinical research studies, including study start-up, monitoring, and closure.,Ensure compliance with regulatory guidelines and industry standards, such as ICH-GCP, ICG, and local regulations.,Coordinate with study teams, including investigators, site personnel, and regulatory affairs, to ensure smooth study execution.,Monitor study progress, identify potential issues, and implement corrective actions as needed.,Prepare and maintain comprehensive study documentation, including source documents, case report forms (CRFs), and other relevant records.,Conduct audits and inspections to ensure compliance with regulatory requirements and internal policies.,Provide training and support to study team members, as needed.,Stay updated with the latest industry trends, regulations, and best practices in clinical research.

🎓 Kualifikasi & Syarat

Bachelor's degree in a relevant field, such as Pharmacy, Medicine, or a related discipline.,Minimum of 5 years of experience in clinical research, with at least 2 years in a senior or leadership role.,Strong understanding of regulatory guidelines, such as ICH-GCP, ICG, and local regulations.,Excellent communication, organizational, and project management skills.,Proficiency in English, both written and spoken.,Experience with electronic data capture (EDC) systems and data management tools.,Knowledge of Good Clinical Practice (GCP) and Good Documentation Practices (GDP).,Ability to work independently and manage multiple tasks and priorities.

🛠️ Keahlian

Clinical research experienceRegulatory affairs knowledgeProject management skillsData management and EDC systemsTraining and mentoring skillsStrong communication and interpersonal skills
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