🎯 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