Senior Clinical Trial Manager
2 weeks ago
Position Description
Job Title:
Senior Clinical Trial Manager
Location:
Cape Town, South Africa; or South Africa-Remote
Reports to:
Associate Director, Clinical Operations
Position Summary:
Help IAVI translate science into global health impact as a Senior Clinical Trial Manager
IAVI is seeking a highly motivated Senior Clinical Trial Manager (CTM) who will manage, oversee and execute day-to-day operational activities for the conduct of clinical trials according to ICH/GCP guidelines and relevant regulatory guidelines.
CTM will lead clinical operations of early and late phase and/or highly complex clinical trials, mentor other clinical operations staff, and lead process improvement.
Key Responsibilities:
- Act as clinical operations lead on project teams for assigned studies.
- Develop the protocol management plan (PMP) and coordinate the development of operations plans for all applicable functions for inclusion in the PMP.
- Develop study timelines and ensure adherence to timelines. Escalates concerns / issues related to timelines to senior management appropriately.
- Lead clinical trial team meetings and contribute clinical updates to crossfunctional project team meetings.
- Oversee the evaluation, development, setup, training, and monitoring of investigational sites participating in epidemiology studies and clinical trials.
- With oversight from the Associate Director / Director, Clinical Operations, develop and control study budgets, working with other departments as appropriate, to ensure execution of studies within budget.; escalate concerns/issues related to budget management to senior management appropriately.
- Together with Associate Director / Director, Clinical Operations, determine which services will be conducted by IAVI and which will be outsourced to other vendors and assists in the identification, evaluation and selection of CROs and other vendors as needed.
- Proactively anticipate risks and plans for and implements risk mitigation strategies throughout the trial conduct.
- Actively manage issues that could impact study progress and takes action or makes recommendations to solve issues to support compliance with expected standards, keeping senior management informed appropriately.
- With oversight from the Associate Director / Director, Clinical Operations, coordinate and develop study protocols.
- With oversight from the Associate Director / Director, Clinical Operations, develop Informed Consent Documents, Study Operations Manual, monitoring plan, tracking forms, and other study related documents as required.
- Lead implementation of riskbased monitoring for assigned studies and liaise with sites and IAVI CRAs and data management to perform data reviews and resolve data queries.
- Review and approve monitoring visit reports submitted by CRAs for assigned studies.
- Complete monitoring oversight visits as needed to review clinical data for accuracy and completeness and resolve discrepancies in accordance with the study monitoring plan.
- Maintain good relations with IAVI collaborators and trial sites to facilitate site development and execution of clinical trials.
- Mentor and train CRAs and Clinical Trial Associates, Clinical Operations Specialists and Clinical Trial Managers as needed.
- When assigned a trial with a Clinical Operations Specialist (COS), delegate clearly defined clinical trial management activities to the COS and ensure deliverables are met with appropriate timeliness and quality.
- Contribute to the Clinical Development (CD) departmental Standard Operating Procedures for conduct of clinical trials based on IAVI templates and ensures adherence to regulations/guidelines for GCP.
- When applicable, act as a member of the CD SOP task force.
- Perform other duties as assigned by the manager.
Education and Work Experience:
- Bachelor's degree in a scientific or other relevant field is required. An advanced degree in relevant field is preferred.
- Minimum 7 years' experience in clinical trial operations, including 4 years in clinical trial management or equivalent experience at study sponsor or CRO is required.
Qualifications and Skills:
- Experience and knowledge of clinical research operations, Good Documentation Practices, ICH GCP, FDA CFR and other relevant regulations as well as Declaration of Helsinki and relevant countryspecific regulations is required.
- Project management experience and ability to deliver on assigned tasks within deadline are required.
- Experience leading multidisciplinary clinical trial teams effectively to deliver clinical trials at high quality, on time and within budget is required.
- Strong interpersonal skills and ability to work effectively with outside vendors, collaborators, subordinates and functional peer groups at various management levels.
- Experience working on problems of high complexity and diverse scope using good judgment within defined procedures and policies to determine ap
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