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The project manager/study coordinator is responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol, and the site’s standard operating proceduresOversee all operations in the clinical trial to ensure protocol and GCP complianceManage regulatory updates throughout the study
Proactively resolve protocol queries and missing data with Investigators and Clinical Trials AssistantsPrepare for and manage participant visits and data capturing in line with protocol and site SOPsAssist in patient recruitment, screening, and enrolment of eligible patients according to protocol requirementsCommunicate well with investigators regarding participant welfare while on study
Notify relevant parties of Serious Adverse Events or Events of Medical Importance as per protocol requirements. Quality control of patient files and data entries Manage site monitoring visits/audits or similarAssist team members and support teams with an open helpful attitude, perform on-the-job training where necessary
Assist the team with ad hoc assignments and duties as needed, delegated by the line manager and within the scope of practiceDegree in Health-Related FieldDesirable additional education, work experience, and personal abilities:Experience in Network studiesOrdered and systematic in approach to tasks, with strict compliance to protocols
Exceptional organizational and administrative skills are required together with working knowledge of Microsoft OfficeAbility to prioritize own workload, take initiative , and work to tight deadlinesOvertime and traveling will be required from time to timeOnly if you do meet the minimum job requirements and experience as mentioned above, you may submit a detailed updated CV.
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