Deskripsi Pekerjaan
Join Clinical Research Malaysia as a Study Coordinator and become a vital contributor to pioneering clinical trials and sponsored research initiatives. In this dynamic role, you'll orchestrate the execution of complex clinical studies, ensuring adherence to regulatory standards and ethical protocols while driving medical innovation forward. Your expertise will directly impact patient outcomes and the advancement of healthcare solutions through meticulous trial coordination, data integrity, and cross-functional collaboration. This opportunity offers a unique platform to work at the intersection of scientific research and patient care in Malaysia's premier clinical research environment.
Tanggung Jawab
- Coordinate end-to-end clinical trial execution including patient recruitment, screening, and informed consent processes
- Maintain accurate regulatory documentation ensuring compliance with GCP, ICH guidelines, and local ethics committee requirements
- Monitor trial progress, track adverse events, and prepare comprehensive study reports for sponsors and stakeholders
- Liaise with investigators, research teams, and sponsors to ensure protocol adherence and timely milestone achievement
- Manage study budgets, equipment logistics, and site visit coordination for multi-center trials
- Implement data management systems to ensure accurate collection, verification, and reporting of clinical data
- Conduct investigator meetings and training sessions to standardize trial procedures across sites
Kualifikasi
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related health sciences field
- Minimum 2 years of clinical research coordination experience in GCP-compliant environments
- Certification in Good Clinical Practice (GCP) and familiarity with local regulatory frameworks
- Proficiency in electronic data capture systems (EDC) and clinical trial management software
- Strong organizational skills with ability to manage multiple concurrent trials and deadlines
- Excellent written and verbal communication skills for stakeholder engagement and documentation
- Detail-oriented approach to protocol adherence, data integrity, and documentation standards
- Knowledge of Malaysian healthcare system and clinical trial landscape preferred