This role is responsible for leading operational activities of clinical trials well as encouraging strong, positive relationships with colleagues across the organization
Job Summary
This role is responsible for leading operational activities of clinical trials well as encouraging strong, positive relationships with colleagues across the organization.
The Senior Clinical Trial Specialist ensures inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), and applicable regulations and guidelines from study start-up through clinical study report.
Employees are eligible for a comprehensive benefits package including retirement plans, long-term incentive program, vacation, sick time, holiday pay, and various leave options.
Matching Summary
This role is responsible for leading operational activities of clinical trials well as encouraging strong, positive relationships with colleagues across the organization.
Salary
Base: $109,000.00 - $174,800.00; Bonus/Equity: Not specified; Benefits: Vacation –120 hours per calendar year, Sick time - 40-56 hours per calendar year, Holiday pay –13 days per calendar year, Work, Personal and Family Time - up to 40 hours per calendar year, Parental Leave – 480 hours, Bereavement Leave – 240 hours/40 hours, Caregiver Leave – 80 hours, Volunteer Leave – 32 hours, Military Spouse Time-Off – 80 hours
Skills & Requirements
Must-have
Clinical trial protocol compliance
GCP and regulatory adherence
Site monitoring activities
Clinical trial document development
Investigational device management
Adverse Event reporting
Nice-to-have
Cross-functional collaboration
Global evidence generation strategies
Problem-solving during study execution
Inclusive work environment
Key Requirements
Minimum 4 years professional work experience
Previous clinical research experience
Previous medical device site monitoring experience
Bachelor's degree in Life Science or related field