Trial Capabilities Associate

Location: Petaling Jaya

Job Descriptions:

• To collect and submit regulatory documents to the Ethics Review Board and Competent Authority, communicate and negotiate budgets and contracts with site
• Track and ensure site compliance to required training and effectively drive timelines aligned with a company priority
• To ensure the investigator sites meet requirements to enroll study participants into clinical trials and support ongoing activities during site maintenance and close-out
• Ensure country specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems
• To obtain clinical trial authorizations and ethical approvals, execution of the budget and contract, records management, and site training
• Provide feedback and shared learning for continuous improvement

Job Requirements:

• Bachelor’s degree, preferably in a scientific or health-related field
• 1-2 years of clinical research experience or relevant experience preferred
• Applicant with the understanding of the overall clinical development paradigm and the importance of efficient site activation
• Applicant with knowledge of project management processes and skills
• Applicants with experience in compliance-driven environment is good
• Excellent English language skills (comprehension, speaking, reading, and writing)
• Effective communication and problem-solving skills
• Good organization and time management skills

Others Information:

For those who have what it takes, please send in resume to:
Recruitment Consultant : Janice Lim
Email: janice@brightprospect.com.my