Senior Clinical Trial Specialist – Remote Position

About the position

Responsibilities
• Ensures timely and accurate study-related communication to clinical personnel (eg, internal and external study teams, consultants and investigative site personnel); prepares and disseminates clinical trial correspondence, newsletters, and IND safety letters (working with project clinician); and assists with the creation of study-specific manuals, tools, and templates
• Participates in selection and management/oversight of external vendors and develops vendor specifications; reviews vendor reports, budgets, and metrics; acts as liaison between vendors and sites (eg, assists sites with laboratory sample queries)
• Coordinates specified clinical trial meetings (eg, investigator meetings, study team meetings, CRA and CRO meetings) by arranging logistics, preparing necessary materials and recording and distributing minutes
• Sets up, tracks, collects and maintains audit-ready clinical trial documentation and study status in an electronic system; manages and tracks regulatory/IRB/IEC documentation, IND safety letter distribution, confidentiality disclosure agreements, and other clinical trial documents; performs initial QC of electronic data feeds; generates, reviews and distributes reports; assists with quality assurance audits and resolution of audit findings.
• Participates in study design and execution by contributing operational experience and expertise: provides input into protocol, ICF, CRF design, monitoring conventions, edit checks and vendor specifications; assists with study or site feasibility process; posts and maintains study-related information on external websites when applicable
• Ensures that necessary study supplies are available as per study timelines: sources clinical trial supplies through external vendors (eg, case report forms, study manuals, lab kits); manages, reviews and tracks drug shipment, destruction, and return; coordinates internal lab sample supply set-up and shipment
• Maintains ongoing communication with site staff to resolve issues (eg, data queries, study management), support the staff, oversee the efficient conduct of the trial, and ensure continued compliance
• May also be responsible for acting as a central point of communication between Puma and investigative sites for all assigned clinical trial-related activities to assure trials are conducted on time and budget, while fully compliant with ICH GCP and the SOPs in effect.
• Conducting on-site visits consistent with the applicable Clinical Monitoring Plan and SOPs for site qualification, site initiation, routine monitoring, site close-out and other site visits (eg, booster), as requested
• Overseeing site recruitment, implementing appropriate contingency plans, as needed
• Assessing site performance and conducting training/re-training when necessary to ensure site compliance with the protocol, applicable regulations and Puma expectations
• Writing confirmation letters, follow-up letters and site visit reports that conform with guidelines and timelines stated in the applicable Clinical Monitoring Plan and SOPs
• Mentors more junior staff
• Manages study team meetings in absence of Clinical Trial Manager
• Performs other tasks, as assigned by the manager/designee to promote the efficient conduct of the trial

Requirements
• Bachelor’s degree or equivalent combination of education/experience, preferably in science or a health-related field
• Strong understanding of GCP, ICH and knowledge of regulatory requirements
• Minimum one year prior Clinical Trial Specialist experience or commensurate

Nice-to-haves
• One year of clinical research experience or health-related experience (eg, study coordinator, data management, nursing)
• Completion of Puma Field Monitoring Course or equivalent, as required for field monitoring activities
• Oncology experience
• Global trial experience

Benefits
• Base compensation range for this position is $85,000k – $105,000k per year, higher compensation may be available for someone with advanced skills and/or experience.