Clinical Research Project Manager

Company Description

ClinActis is a full-service contract research organization (CRO) specializing in clinical trial services across the Asia Pacific region for pharmaceutical, medical device, medical nutrition, and biotech companies. Founded in 2009 and headquartered in Singapore, ClinActis boasts a team with over 50 cumulative years of clinical research experience. With expertise in global clinical trials and in-depth knowledge of local regulations, cultures, and healthcare systems, ClinActis delivers customized solutions tailored to regional and client-specific requirements. The company offers end-to-end trial services, including study design, protocol development, site selection, data management, and regulatory affairs, all aimed at ensuring a seamless clinical trial experience in the APAC region. ClinActis is dedicated to helping clients bring safe and effective medical innovations to market efficiently.

Role Description

This is a role for a Clinical Research Project Manager. The role includes managing clinical trial projects, reviewing study protocols, overseeing project timelines and budgets, coordinating with multidisciplinary teams, and monitoring trial progress to ensure compliance with regulations and standards. The Clinical Research Project Manager will also collaborate with stakeholders, manage trial data, and resolve any project-related issues to ensure successful trial outcomes.

Qualifications

• Experience and skills in Trial Management and overseeing clinical study operations
• Proficiency in developing and reviewing Protocols and related clinical documentation
• Strong Project Management skills, including coordination, budgeting, and timeline oversight
• Knowledge and expertise in Research methodologies and best practices in clinical studies
• Competence in Data Management, including maintaining data integrity and ensuring regulatory compliance
• Strong communication, organizational, and problem-solving skills
• Bachelor's or Master's degree in life sciences or related field
• Experience in clinical research in the Asia-Pacific region is highly desirable
• Knowledge of regulatory requirements and international guidelines (e.g., ICH-GCP) is an advantage