Job Overview :
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
Education / Qualifications :
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.
Phase 1 & Oncology experience highly desirable.