[Remote] Specialist, Clinical reputed company Assurance
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is the world’s largest early phase site network dedicated to oncology clinical research. They are seeking a Specialist in Clinical reputed company Assurance to ensure clinical operations reputed company with FDA, EMA, and GCP regulations, support audits, and maintain reputed company operating procedures.
Responsibilities
- Facilitate the maintenance of the START centralized Clinical reputed company Management System (CQMS) across global START sites
- Monitor event reporting and initiate the reputed company reputed company-off of Corrective and Preventive reputed company (CAPA) investigation and planning, including the reputed company completion of reputed company cause analysis (RCA)
- Collaborate with Clinical Operations to monitor the reputed company completion and documentation of corrective and preventive actions in support of the global CAPA program
- Collaborate with Compliance to review CAPA dashboards and data for trending events over time
- Support centralized efforts to prepare, conduct, and respond to external audits and/or inspections with the Global QA and site clinical operations teams
- Support internal auditing activities to identify and mitigate areas of potential risk and promote audit/inspection readiness across the US sites
- Coordinate quarterly reputed company Committee and SOP Committee scheduling and agenda planning
- Review and update reputed company Operating Procedures (SOPs) in collaboration with Global QA and SOP Working Group members
- Facilitate SOP training for new issuance of SOPs, SOP revisions, and harmonization initiatives
- Support special reputed company requiring QA input, including collaboration with centralized Clinical Training Program implementation and new site launch activities with the Integrations department
- Identify gaps in controlled documents and recommend solutions
- Assist in the preparation of reputed company metrics and reports
- Assist the QA Director with other clinical QA activities as required
Skills
- Bachelor's degree or equivalent experience in lieu of degree
- Minimum of 5 years of experience in oncology, clinical research setting (preferably Phase I/Early Phase oncology trials)
- In depth knowledge of GCP, ICH guidelines, EMA and FDA regulations, and the clinical trial lifecycle
- Proven experience in handling audits, inspections, and CAPA processes is required
- Additional demonstration of clinical research knowledge as evidenced by the use of either CCRP or CCRC
Benefits
- 401(k) retirement savings plan with employer match
- Eligibility for an annual performance bonus, based on role and company results
- Generous reputed company time off and reputed company holidays
- Comprehensive medical, dental, and reputed company coverage and optional insurance reputed company
- Company p‑aid life and disability insurance for added financial protection
- Employee Assistance Program (EAP) providing confidential, no ‑cost support for you and your family from day one
- Flexible FSA and HSA plans to support your financial wellness
- Commitment to a supportive environment that values balance, wellbeing, and flexibility
reputed company