Clinical Trial Leader

Ethicon, part of the Johnson & Johnson Medical Devices Companies, is recruiting for a Clinical Trial Leader located in Cincinnati, OH, or Raritan, NJ. Remote work options may be considered on a case-by-case basis and if approved by the Company. Ethicon, part of the Johnson & Johnson Medical Devices Companies, has made significant contributions to surgery for more than 60 years from creating the first sutures, to revolutionizing surgery with minimally invasive procedures. Our continuing dedication to Shape the Future of Surgery is built on our commitment to help address the world's most pressing health care issues and improve and save more lives. Through Ethicon's surgical technologies and solutions including sutures, staplers, energy devices, trocars and hemostats and our commitment to treat serious medical conditions like obesity and cancer worldwide, we deliver innovation to make a life-changing impact. For more information, visit www.ethicon.com. This individual will be responsible for leading one or more clinical trials within the R&D Clinical Operations group, as well as fostering strong, productive relationships with colleagues across the organization. Key Responsibilities: Serves as a Clinical Trial Leader within the R&D Clinical Operations group to execute company sponsored clinical trials for the Ethicon Medical Device Franchise Leads all operational activities of assigned clinical studies Serves as a member of the clinical trial/study core team, and serves as the liaison with Clinical Franchise and Clinical Biometrics for assigned clinical trials Provides internal communication of important clinical data and events. Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by business partners Is accountable for quality, compliance with regulations and company procedures, timelines, and budgets for assigned clinical trials Solves problems with support from Clinical Management arising during clinical study execution, and will seek mentorship for more complex situations, as needed Supports the development/implementation of new clinical systems/processes, and provides support for cross sector clinical operations initiatives, as needed Interacts and collaborates with site personnel, IRBs/ECs, Competent Authorities/MoH, contractors/vendors, and company personnel Ensures efficient use of resources within the clinical study/program to provide high quality results Provides direction to and oversight of Clinical Research Associates/Site Monitors, as it relates to clinical trial conduct May provide direct oversight of CRO(s) or other vendors as needed for assigned clinical trials May serve as the primary contact for clinical trial sites May review and provide input on clinical operation section of protocols May be involved in other tasks to support R&D Clinical Operations and R&D Clinical Franchise as needed Ensures that all Human Resource related activities, and decisions embody the Johnson & Johnson Credo Values Qualifications Education: Bachelor’s degree in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy) preferred, or equivalent experience. Required: 2-4 years of clinical research experience acquired in medical device or pharmaceutical industry, CRO or investigational site. Previous experience in clinical trial management or equivalent Understanding and application of Good Clinical Practices Preferred: Relevant industry certifications (i.e., CCRA, RAC, CDE). Clinical/medical background Medical device experience Other: This position may require up to 10% travel, primarily for meetings. At Johnson & Johnson, we’re on a mission to change the trajectory of health for humanity. That starts by creating the world’s healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional, and financial health of our employees and the ones they love. As such, candidates offered employment must show proof of COVID-19 vaccination or secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families, and the communities in which we live and work. For more information on how we support the whole health of our employees throughout their wellness, career, and life journey, please visit www.careers.jnj.com. The anticipated base pay range for this position is $66,000 to midpoint $92,000. The Company maintains highly competitive, performance-based compensation programs. Under current guidelines, this position is eligible for an annual performance bonus. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/performance year. Bonuses are awarded at the Company’s discretion on an individual basis. Employees may be eligible to participate in Company employee benefit programs such as health insurance, savings plan, pension plan, disability plan, vacation pay, sick time, holiday pay, and work, personal and family time off in accordance with the terms of the applicable plans. Additional information can be found through the link below. Information on benefits can be viewed by following this link: https://www.careers.jnj.com/employee-benefits Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Primary Location United States-Ohio-Cincinnati-4545 Creek Road Other Locations North America-United States-New Jersey Organization Ethicon Endo Surgery Inc (6041) Job Function R&D Requisition ID 2206061750W