Site Management Associate II

This is a fully remote position, open to applicants in Malaysia.

📋 Description

• Assist in the oversight and evaluation of clinical trial locations.

• Ensure adherence to study protocols, regulatory standards, and Good Clinical Practice (GCP) guidelines.

• Coordinate monitoring efforts at clinical trial sites and address site-related challenges.

• Aid in the preparation and assessment of regulatory documents.

• Work collaboratively with cross-functional teams throughout the duration of the study.

• Monitor site performance metrics, analyze data, and generate reports.

• Engage in training programs and provide mentorship to junior team members.

⛳️ Requirements

• A bachelor's degree in a pertinent field such as life sciences, healthcare administration, or clinical research.

• Background in clinical research, site management, or monitoring, with a comprehensive understanding of clinical trial processes and GCP guidelines.

• Strong organizational and project management capabilities, with the capacity to manage multiple priorities and deadlines.

• Outstanding analytical skills and meticulous attention to detail, emphasizing the maintenance of high-quality standards.

• Excellent communication and interpersonal skills, with the ability to cultivate and sustain effective relationships with site personnel and cross-functional teams.

• Openness to travel as necessary (approximately 25%).

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.