Manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.
Plan and manage all Clinical Operations aspects of clinical trials/studies, ensuring adherence to timelines, budget, and quality standards.
Collaborate with global cross-functional teams to establish and implement clinical trial/study protocols and procedures.
Build and manage strong relationships with investigators and stakeholders.
Ensure all trials/studies are conducted in compliance with local, national, and international regulations and ethical guidelines.
Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.
Lead the clinical team to deliver the study in accordance with sponsors expectations.

University degree in medicine, science, or equivalent combination of education & experience
At least 2 years’ experience in the similar role / in CRO or Pharma company
Demonstrated ability to drive the clinical deliverables of a study
Worked across different clinical studies in various therapeutic areas in Phases III and/or IV
Prior experience with risk-based monitoring (RBM) oversight is desirable
Willingness to travel as required (approximately 15%)
Ability to work on multiple project/clients simultaneously on assigned FTE
Strong time management skills
Experience in non-interventional studies is a plus but not required.

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

Clinical Trial Manager

Key skills