Clinical Research Site Manager
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# Clinical Research Site ManagerChronic Pain Research InstituteFull TimejuniorCharlotte, North Carolina, USPosted Yesterday## Role OverviewChronic Pain Research Institute is hiring a entry-level Clinical Research Site Manager. This is a full-time role in Charlotte. posted yesterday. Full responsibilities, required qualifications, and the apply link are listed in the description below.## Resume Keywords to IncludeMake sure these keywords appear in your resume to improve ATS scoringGCPBudgetingORCompensationBenefitsComplianceClinicalResearchSign up free to auto-tailor your resume with all these keywords and get a higher ATS score## Job description Clinical Research ManagerLocation: Raleigh, NCEmployment Type: Full-TimePosted by: chronic Pain Research Institute on behalf of Client About the OpportunityOur client is a highly respected neurosurgery and interventional pain management group that is launching an innovative clinical research center. This is a unique opportunity to join at the ground level and play a pivotal role in building and leading a growing research program focused on advancing therapies in neurology, pain management, and medical devices.We are seeking a Clinical Research Manager to oversee and develop all aspects of the research operations. The ideal candidate is experienced, organized, and passionate about clinical research, with the ability to lead teams and establish efficient processes from the ground up. Key Responsibilities* Lead the startup, development, and day-to-day management of clinical research operations* Oversee clinical trials, including device and drug studies, ensuring compliance with protocols, GCP, and regulatory requirements* Manage and mentor clinical research staff (coordinators, assistants, regulatory personnel)* Develop and implement SOPs, workflows, and quality systems* Act as primary liaison with sponsors, CROs, IRBs, and regulatory bodies* Ensure accurate data collection, documentation, and reporting* Oversee budgeting, study feasibility, and financial management of trials* Prepare for and manage audits and monitoring visits* Support site growth strategy, including study selection and startup activities Qualifications* Bachelor’s degree required (life sciences, nursing, or related field preferred)* 5+ years of clinical research experience, with at least 2 years in a leadership or management role* Strong knowledge of FDA regulations, ICH-GCP, and clinical trial processes* Experience in neurosurgery, pain management, CNS, or medical device trials strongly preferred* Proven ability to build and manage research programs or teams* Excellent organizational, communication, and leadership skillsCertifications such as CCRC, CCRP, or CPI are a plus. Why This Role?* Ground-floor leadership role in a brand-new research center* Work alongside a highly reputable physician group* Opportunity to shape and grow a cutting-edge clinical research program* Competitive compensation and benefits* Meaningful impact on advancing treatments for patients in need How to ApplyApply directly via LinkedIn or send your resume to: View email address on click.appcast.io #J-18808-Ljbffr
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Dormont Manufacturing Co is seeking an experienced Clinical Research Coordinator to manage clinical trials at Peninsula Research Associates in North Carolina. The role involves ensuring compliance, conducting patient visits, and maintaining regulatory documentation. Ideal...- Dormont Manufacturing Co in North Carolina is seeking a Clinical Research Coordinator for overseeing clinical research protocols focused on hematology malignancies. The role entails coordinating study activities, assessing patient eligibility, and ensuring data integrity...
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