Key Responsibilities:
Act as primary point of contact to lead, manage and coordinate the conduct of clinical trials from study start-up to close out at a country level in accordance with ICH-GCP and applicable local regulations.
Provide direction and guidance to the project team, coordinating site management and
monitoring activities, and communicating status of these activities to the Project Manager (PM). You will be required to maintain the quality and scientific integrity of clinical trials at a country level.
Actively collaborate with cross functional stakeholders to ensure timely and on budget execution of clinical trial deliverables within the county.
Qualifications:
Bachelor or Master’s degree in Science, Pharmacy, Nurse
More than 7 years of CRA experience with at least 2 years of experience in leading internal CRA at an advanced level and demonstrated effective leadership and organization and communicated skills.
English proficiency level
Able to travel upcountry