Senior Clinical Research Coordinator

Senior Clinical Research CoordinatorWe believe that great healthcare is an essential safeguard of human dignity. At Laborie, we know the work we do matters – it's what fuels our motivation and contributes to our success. If you're ready to make a positive impact in the lives of patients across the globe, we'd like to meet you. We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We're not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.About the Role:Develop and monitor study operational metrics, key performance identifiers, and compliance risks as assigned; collaborate with study teams to mitigate risks.Participate in departmental initiatives to improve operational efficiency and quality.Lead end-to-end trial master file strategy and execution for assigned studies.Oversee department payment processes for assigned studies.Monitor payment compliance, forecasting, tracking, and reconciliation activities.Lead and manage administration and timelines, proactively identify and mitigate delays, and ensure timely execution of clinical, vendor/CRO service, consultant, and related agreements.Coordinate and support study- and department-related meetings, including developing agendas, preparing materials, and documenting and distributing meeting minutes.Minimum Qualifications:Bachelor's degree in Life Sciences, Health Sciences, Business Administration, or a related field, or equivalent combination of education and experience.4-6 years of clinical research, clinical operations, trial master file management, contract administration, or related experience; medical device, pharmaceutical, or biotechnology industry experience preferred.Experience independently managing clinical study documentation and operational processes.Demonstrated ability to lead complex operational activities with minimal supervision.Strong knowledge of ICH-GCP, trial master file requirements, and clinical research regulations.Proficiency with eTMF systems, contract tracking tools, and Microsoft Office applications.Advanced understanding of clinical trial documentation, contracts, and payment processes.Excellent organizational, communication, and stakeholder management skills with strong analytical and problem-solving skills.Ability to identify risks, influence outcomes, and drive process improvements.Laborie's Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.Paid time off and paid volunteer timeMedical, Dental, Vision and Flexible Spending AccountHealth Savings Account with Company Funded Contributions401k Retirement Plan with Company MatchParental Leave and Adoption ServicesHealth and Wellness Programs and EventsAwarded 2025 Cigna Healthy Workforce Designation Gold LevelLaborie provides equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.