YOUR TASKS AND RESPONSIBILITIES:

Lead a team of clinical research professionals and collaborate with cross-functional stakeholders. Develop and implement project plans, including timelines, milestones, and resource allocation. Define project objectives, deliverables, and success criteria in collaboration with stakeholders. Identify risks and develop mitigation strategies to ensure project success. Allocate resources, assign tasks, and monitor team performance to ensure project goals are met. Develop project budgets, track expenses, and ensure cost-effective utilization of resources. Collaborate with finance and procurement teams to manage contracts, vendor selection, and outsourcing activities. Monitor project progress and resource allocation to ensure efficient utilization and adherence to budgetary guidelines. Ensure adherence to applicable regulatory guidelines, Good Clinical Practice (GCP), and other relevant standards. Oversee the preparation and submission of regulatory documents to ethics committees and regulatory authorities. Implement quality control measures to ensure data integrity, accuracy, and compliance throughout the project

 

WHO YOU ARE:

Minimum requirement is a Bachelor's or Master's degree in a field related to Science, Healthcare, Clinical Research or Life Sciences like Biology, Pharmacology, Nursing, or a related discipline, and/or Post-graduate Diploma in Clinical Research. Relevant experience of 5-10 years minimum in the field of Clinical Research.