Job Description

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

• 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.