The Clinical Team Lead (CTL) is the leader for the clinical team in our Clinical Operations ONCOLOGY CTL group. The Clinical Team Lead (CTL) is responsible and accountable for the execution of the clinical operations component of the project, at the global or regional level, as assigned. The CTL is responsible for working cross functionally, within a matrix environment, to ensure successful execution of the trial including oversight of the clinical operations from a quality, timeline, budget and scope perspective.
The CTL position can be home based anywhere within the United States or Canada.
Other therapeutic areas of focus for the CTL position are ophthalmology, rare disease, or liver disease/NASH.
Essential Job Duties:
- Responsible and accountable for the management of the Clinical Operations team with particular emphasis on teamwork, quality, timelines, budget, metrics and compliance with the project plans and SOPs.
- Develop the strategy, plans, tools and training to oversee and assess performance of the clinical team, in the conduct and compliance of site visits (on site and remote), including, but not limited to: Pre-Study Visits, Site Initiation Visits, Routine Monitoring Visit, Motivational Visits, Close-out Visits, Audit support Visits.
- Proactively communicate with CRAs and other members of the clinical operations team to follow up on all open issues, drive patient recruitment and retention, in order to meet the project timelines.
- Ensure that all study related, clinical related documents are tracked, filed and reviewed (QC check) and complete according to the SOPs, regulatory requirements and protocol.
- Responsible and accountable for understanding and managing the clinical operations budget for the project, and ensure that the activities are within budget and scope of work, and to discuss with the project team to support financial progress, and team utilization.
- Communicate effectively with all members of the project team and client as applicable, to support the study completion per company and client requirements and timelines, including risk identification and mitigation, issue escalation and working with Quality and the project team on Corrective and Preventative Actions.
- As required by the project roles participate and oversee the site selection process. Depending on the scope and roles within the project team, this may be performed in collaboration with other team members.
- As required by the project roles participate and oversee the regulatory/ethics committee submissions, tracking and documentation.
- Support new business with active participation in Bid Defense preparation and meetings, as required.
- Perform other duties as required by the Department or Project Team.
•BSc or BA degree in a biomedical or related life science, or nursing qualification.
•Or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
•0-4 years' experience as a CTL, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
•Minimum 4+ years CRA experience, on-site or in-house.
•In lieu of the above minimum requirement, candidates with 6 or more years of relevant clinical research experience in pharmaceutical, CRO or health care setting will be considered.
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