Key skills
Mentoring
About this role
Role Overview
- Manage clinical trial operations activities
- Coordinate clinical trial management delivery
- Resolve issues and develop team capability
- Oversee the clinical portion of the budget to ensure efficient resource allocation
- Develop monitoring plans and tools, ensuring effective study oversight
- Train and mentor Clinical Research Associates (CRAs) to optimize their performance
- Drive enrollment and lead study start-up activities, adhering to timelines
- Review trip reports and implement corrective and preventative action plans when necessary
- Foster productive relationships with Sponsors, vendors, and cross-functional teams
Requirements
- A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization
- Bachelor's degree in health, life sciences, or other relevant fields of study
- At least 10+ years of relevant experience in clinical trial management
- Preferred: 2+ years of monitoring experience
- Experience in managing complex or global trials is advantageous
- Preferred: Experience in managing all trial components from start-up to database lock
- Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives
- Willingness to travel as required (approximately 25%)
Benefits
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways