Clinical Trial Assistant I

Résumé du poste

The Clinical Trial Assistant will support clinical trial operations by managing essential documentation, maintaining TMF and CTMS systems, and coordinating with study sites and vendors. They will also assist in regulatory submissions, site monitoring compliance, and the preparation of clinical trial reports.

Détails du poste

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today. Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s Corporate headquarters are located in Ontario, Canada and US headquarters in New Jersey, USA, with additional physical offices in Asia and Europe. Everest is known in the industry for its high-quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success. Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s Everest. To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as a Clinical Trial Assistant for our Toronto/Markham, Ontario, Canada on-site location, or remotely from a home-based office anywhere in Canada in accordance with our Work from Home policy. Job Accountabilities: 1. Interact with study Sponsors, investigational sites, vendors, and Everest functional groups to enable timely and high-quality operationalization of clinical trials in compliance with ICH-GCP and relevant local regulations. 2. Compile documentation for qualification of clinical sites. Support review of that documentation to ensure that those clinical sites comply with ICH-GCP and relevant local regulations. 3. Assist with preparation and submission of regulatory documents to responsible authorities and Institutional Review Boards/Ethics Committees. 4. Responsible for set-up, maintenance, and archival of studies in the Trial Master File (TMF) and Clinical Trial Management System (CTMS). 5. Establish, maintain, and archive files of essential documents from investigative sites and for inclusion in TMF. These files must be maintained in a fashion so that they are continuously available for inspection and completion for archive. 6. Assist with site identification, feasibility questionnaire development and distribution, and site selection. 7. Contribute to the development of Clinical Operations documents (i.e., Investigator Site File logs, newsletters, etc.) to facilitate the implementation and management of the clinical trial. 8. Collaborate with meeting planners and vendors to arrange for Investigator meetings, off-site client meetings (i.e., kick-off meetings), or internal departmental meetings. 9. Responsible for the shipment and tracking of trial documents (site binders, manuals, guides, etc.) and supplies, as needed. 10. Track monitoring plan compliance metrics (i.e., monitoring frequency and monitoring visit report submission/finalization). Issue reminders to monitoring team. 11. Distribute Suspected Unexpected Serious Adverse Reactions (SUSARs) to investigational sites and complete necessary tracking (acknowledgement of receipts, etc.). 12. Assist with the download of reports from Electronic Data Capture (EDC) systems and Interactive Web Response Systems (IWRS) to prepare summary of data for Project Managers/Clinical Trial Managers. 13. Maintain study portals, web sites, or newsletters. 14. Compile reports progress/status of investigational sites. 15. Assist with processing of vendor/site invoices and Investigator site payments. 16. Participate in the development and maintenance of and adhere to departmental Standard Operations Procedures (SOPs) and guidelines. 17. Collaborate with other team members to prepare, maintain, and complete training on study-specific and/or applicable Sponsor SOPs. 18. Support sites and internal Clinical Operations efforts to prepare for inspections and/or audits conducted either by Everest, Sponsors, or regulatory authorities. 19. Assist Clinical Operations team members with Requests for Proposals and other Clinical Operations tasks as needed. 20. Provide support for Clinical Operations and other functional areas as needed. Qualifications: 1. Bachelor’s degree in Life Sciences or related field of study. 2. Excellent communication (both verbal and written) and computer skills. 3. Expert use of the Microsoft Office suite is essential. 4. Minimum of 1 year of experience in administrative support preferred. 5. Experience in managing and maintaining electronic TMFs. 6. Thorough knowledge of ICH-GCP guidelines and applicable regulations. 7. Ability to travel a maximum of 5% of working hours is required. Benefits & Compensation: We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a pension plan, generous paid time off and sick leave, and the opportunity to earn a performance based bonus. To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.everestclinical.com [http://www.everestclinical.com] Estimated Salary Range: $45,000 - 65,000. We thank all interested applicants, however, only those selected for an interview will be contacted. Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.

Ce que vous ferez

The Clinical Trial Assistant will support clinical trial operations by managing essential documentation, maintaining TMF and CTMS systems, and coordinating with study sites and vendors. They will also assist in regulatory submissions, site monitoring compliance, and the preparation of clinical trial reports.

Exigences

Candidates must hold a Bachelor's degree in Life Sciences or a related field and possess expert proficiency in Microsoft Office. At least one year of administrative experience and a thorough understanding of ICH-GCP guidelines are required.

Avantages

• Medical coverage • Dental coverage • Vision coverage • Life insurance • AD&D insurance • Short-term disability • Long-term disability • Tuition reimbursement • Fitness reimbursement • Employee assistance program • Pension plan • Paid time off • Sick leave • Performance based bonus

Compétences indiquées

• Administrative Support · Souhaitée
• Vendor Coordination · Souhaitée
• Communication Skills · Souhaitée
• Microsoft Office Suite · Souhaitée
• data management · Souhaitée

Autres compétences pertinentes

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Clinical trial operations
• ICH-GCP compliance
• Trial Master File management
• CTMS
• Regulatory document submission
• Site qualification
• Site selection
• Electronic Data Capture
• IWRS
• Administrative support
• Microsoft Office suite
• Communication skills
• Data management
• Vendor coordination
• Audit support
• Regulatory Documents
• Monitoring Plan
• Administrative Support
• Time Off Management
• Newsletters
• Questionnaire Design
• Ethical Standards And Conduct
• Medical Devices
• Research
• Archive File
• Auditing
• Biotechnology
• Biopharmaceuticals
• Management
• Customer Service
• Clinical Research
• Clinical Trials
• Clinical Trial Management Systems
• Communication
• Computer Literacy
• Data Management
• Electronic Data Capture (EDC)
• Employee Assistance Programs
• Good Clinical Practices (GCP)
• Invoicing
• Life Sciences
• Project Management
• Microsoft Office
• Operations
• Pharmaceuticals
• Request For Proposal
• Site Selection
• Trial Master File

Domaines d’emploi

• Science & Research
• Healthcare
• Administrative
• Clinical Trial Assistant
• Medical Assistant
• Medical Assistants