Mission: Lead and ensure the successful delivery of clinical research projects — from planning through execution — aligned with client expectations, timelines, and quality standards.
Responsibilities:
Manage the full project lifecycle, including resources, timelines, quality, risks, issues, and changes, ensuring delivery within budget and expected outcomes;
Plan, implement, and monitor project progress, coordinating cross-functional teams throughout each phase;
Ensure compliance with international and national regulations, as well as Good Clinical Practice (GCP);
Develop, maintain, and communicate project plans and status updates with departments such as Regulatory, Logistics, Laboratory, Clinical Operations, Finance, and Legal;
Lead, motivate, and develop the project team;
Plan team allocation according to sponsor objectives;
Engage Key Opinion Leaders (KOLs) through meetings, site visits, and ongoing communication;
Identify regulatory opportunities;
Support site selection and build strong, 360º stakeholder relationships;
Manage regulatory submissions and documentation timelines;
Assess study feasibility and ensure execution aligned with KPIs.
Education:
Bachelor’s degree in Health Sciences, Business Administration, Engineering, or related fields;
A postgraduate degree is considered a plus.
Language: Advanced English
⏳ Experience: Minimum of 3 years of experience in Clinical Research Project Management