Clinical Research Fellow 1 Houston Methodist HospitalClinical Research Fellow 1Houston, TXPrepares and delivers educational presentations and deliver written reports of scholarship, including but not limited to, published manuscripts in peer-reviewed journals, quarterly activity reports to fellowship stakeholders, and activity reports to external study sponsors as needed. Houston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval.
Senior Clinical Research Associate (Field- Based) - Multiple Openings NAMSA IncSenior Clinical Research Associate (Field- Based) - Multiple OpeningsNY$68,800–$133,700 / yearAssess the suitability of potential investigative sites through screening interviews, regulatory document review and evaluation of study information and provides input to the site selection process. Supports study start-up activities such as tracking and performing quality review of study documents, completing, and distributing site activation letters, etc.
Director, Clinical Pharmacology and Pharmacokinetics Disc Medicine IncDirector, Clinical Pharmacology and Pharmacokineticsmassachusetts, MA$247,000–$297,000 / yearPOSITION OVERVIEW: Reporting to the Vice President of Clinical Pharmacology the Clinical Pharmacology Lead will provide strategic and scientific leadership across multiple programs at Disc Medicine, serving as the clinical pharmacology representative on cross-functional development teams. Manage and execute clinical pharmacology deliverables in collaboration with internal and external partners in an efficient and scientifically rigorous manner and provide oversight for work conducted by contract research organizations (CROs).
Clinical Research Program Coordinator - Internal Medicine, Cardiology Virginia Commonwealth UniversityClinical Research Program Coordinator - Internal Medicine, CardiologyRichmond, VA$55,000–$62,000 / yearPauley is a regional and national leader in research, education, and clinical programs involving electrophysiology; advanced cardiac imaging (MRI, CT, echo); advanced heart failure, including device-based treatments, total artificial heart, and heart transplant programs; cardio-oncology; high-risk percutaneous coronary interventions; adult congenital heart disease; and exercise-based cardiovascular disease prevention. Pauley''s mission is to improve cardiovascular care and reduce health disparities for all through interdisciplinary, cutting-edge, clinical, translational and community-based research; training and developing the next generation of cardiovascular clinicians and researchers across all levels of education; and providing innovative and accessible cardiovascular procedural care (both surgical and catheter-based) that is the best in the Commonwealth.
Licensed Clinical Research Coordinator (Varying Levels); Cancer Center University of VirginiaLicensed Clinical Research Coordinator (Varying Levels); Cancer CenterCharlottesville, VAThe Office of Clinical Research (OCR) at the University of Virginia Comprehensive Cancer Center is looking for Licensed Clinical Research Coordinators (CRC) to support the advancement of innovative cancer research. This is an excellent opportunity for detail-oriented, collaborative professionals who are passionate about high-quality research and motivated to contribute to work that improves and extends patients' lives.
Clinical Research Coordinator I, Department of Neurology University of ArizonaClinical Research Coordinator I, Department of NeurologyTucson, AZ$47,356–$59,195 / yearCareer Stream and Level PC1 Job Family Clinical Research Job Function Research Type of criminal background check required: Name-based criminal background check (non-security sensitive) Number of Vacancies 1 Target Hire Date Expected End Date Contact Information for Candidates gcbdtv Open Date 8/20/2026 Open Until Filled Yes Documents Needed to Apply Resume and Cover Letter Special Instructions to Applicant. Outstanding U of A benefits include health, dental, and vision insurance plans; life insurance and disability programs; paid vacation, sick leave, and holidays; UA/ASU/NAU tuition reduction for the employee and qualified family members; state retirement plan; access to UA recreation and cultural activities; and more!
NewClinical Research Program Director Children's HospitalClinical Research Program DirectorCollaborates with Clinical Research Investigators to initiate the development of new protocols and coordinate efforts to implement Children’s National Research Institute investigator-initiated trials, industry-sponsored trials and federally sponsored trials, including complex multi-disciplinary protocols that involve multifaceted collaborations with numerous entities. The Program Director demonstrates expert clinical, organizational, and communication skills and functions as a resource regarding the clinical research and/or grants process, and demonstrates expert understanding of the federal and institutional regulations and policies governing clinical research involving protection of human subjects (JCAHO, FDA, ICH, GCP, OHRP, IRB, NIH).
Director Clinical Research (Hybrid) Presbyterian System ServicesDirector Clinical Research (Hybrid)The Director develops and sustains the infrastructure necessary to support a growing enterprise clinical research program and provides executive oversight of research administration, the Human Research Protection Program (HRPP), the Human Research Protections Office (HRPO), research compliance, financial stewardship, operational performance, and strategic partnerships that expand access to innovative clinical research across Presbyterian Healthcare Services. Key Internal Relationships: CEO, Executive Leadership Team, PCLT, Medical Group Leadership, Hospital Leadership, Clinical Program Leadership, Finance, Legal, Compliance, Revenue Cycle, Pharmacy, Quality, Information Services, Population Health, Physician Investigators, Research Staff.
Clinical Research Coordinator II - Rollins School of Public Health Emory UniversityClinical Research Coordinator II - Rollins School of Public HealthAtlanta, GeorgiaFull timeAlthough the position is based in Glynn County, the CRC will interact regularly with the Research Project Manager and study investigators at Emory to provide updates on field operations, identify and resolve issues, and ensure consistent implementation of study protocols. An essential job requirement is that the CRC can build and maintain trusted relationships with study participants and community partners in Glynn County to support participant retention and to fulfill the value of community-engaged research.
NewClinical Research Professional I NE Arkansas Children's HospitalClinical Research Professional I NELittle Rock, AR$23–$28.70 / hourServes as a research resource to subjects, families, and other healthcare providers regarding the needs of study and subjects family preserving patient/subject privacy and maintaining confidentiality of subject information. This role serves as a resource for research study participants, families, other healthcare providers, and members of the clinical research team regarding specified aspects of the study.
Research Coordinator II - Cancer - Clinical Trials Clinical Studies Houston Methodist HospitalResearch Coordinator II - Cancer - Clinical Trials Clinical StudiesHouston, TXHouston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. Under minimal supervision, this position is responsible for ensuring accurate data collection, documentation, organization and safety of research participants, gathering patient data for clinical research activities via methods specified in the study protocol and performs general administrative duties supporting the study.
Clinical Research Coordinator 1/2/3, Neurosurgery University of VirginiaClinical Research Coordinator 1/2/3, NeurosurgeryCharlottesville, VAThe incumbent evaluates the feasibility of proposed trials, prepares and or plans for the opening of trials, conducts trials, facilitates data capture, and audits multiple clinical trials. Maintain proper protocol, consent, amendment, and yearly renewal submission to the Human Investigation Committee, General Clinical Research Center, Radiation Safety Committee and the Office of Grants and Contracts.
Clinical Research Coordinator III - Psychiatry Washington University in St LouisClinical Research Coordinator III - PsychiatryForest Park, GeorgiaProvides study coordinator functions and performs all duties associated with the coordination and implementation of clinical research study/projects, data collection, and the management of data generated by study protocols; consents participants for non-therapeutic clinical trials and performs blood draws and other specimen collection as needed. Clinical Research Management, Clinical Study Protocols, Database Management, Data Entry, Detail-Oriented, Freezerworks (Software), Ordering Supplies, Organizing, Participant Recruiting, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS), Team Supervision, Written Communication Grade .
Clinical Research Coordinator III Winship Cancer Institute Emory UniversityClinical Research Coordinator III Winship Cancer InstituteAtlanta, GACancer care at Winship includes leading cancer specialists collaborating across disciplines to tailor treatment plans to each patient's needs and type of cancer; innovative therapies and clinical trials; comprehensive patient and family support services; and a personalized care experience aimed at easing the burden of cancer. Dedicated to discovering cures for cancer and inspiring hope, Winship Cancer Institute of Emory University is Georgia's only National Cancer Institute-designated Comprehensive Cancer Center, a prestigious distinction given to the top tier of cancer centers nationwide for making breakthroughs against cancer.
Director, Clinical Trials Unit University of VirginiaDirector, Clinical Trials UnitCharlottesville, VAProvide infrastructural support and clinical research expertise to the clinical investigative staff throughout the institution which includes, but is not limited to, protocol and informed consent development, IND/IDE submissions, FDA inspections, and general operational and/or compliance questions. Provide the oversight and management of clinical research mentoring, training and continuing education for all research personnel, including investigators, clinical research coordinators and any ancillary personnel involved in clinical research activities.
FDA Program Administrator/Clinical Research Monitor Virginia Commonwealth UniversityFDA Program Administrator/Clinical Research MonitorRichmond, VA$70,000–$80,000 / yearServe as a back-up for the following: Draft and submit the following submissions to the FDA on behalf of the sponsor-investigators: IND/IDE exemption, IND/IDE initial submission, amendments, annual reports, safety events, closures and single patient/emergency use. We partner with faculty in all schools and departments as they seek funding, plan studies, establish collaborations, calculate budgets, submit grant applications, negotiate industry contracts, and secure patents and licensing agreements.
Clinical Research Coordinator II Rollins School of Public Health Emory UniversityClinical Research Coordinator II Rollins School of Public HealthAtlanta, GAAlthough the position is based in Glynn County, the CRC will interact regularly with the Research Project Manager and study investigators at Emory to provide updates on field operations, identify and resolve issues, and ensure consistent implementation of study protocols. An essential job requirement is that the CRC can build and maintain trusted relationships with study participants and community partners in Glynn County to support participant retention and to fulfill the value of community-engaged research.
NewClinical Research Coordinator III/IV - Bone Marrow Transplantation Cincinnati Children's Hospital Medical CenterClinical Research Coordinator III/IV - Bone Marrow TransplantationCincinnati, OHCreate case report forms (CRFs) in consultation with other team members, as needed, using existing study data information to promote efficient data collection and data entry. Study Conduct/ Clinical Research Practice - Serve as a resource for others for all aspects of conducting a clinical trial for complex and multi-center trials.
Clinical Research Coordinator HCA Healthcare IncClinical Research CoordinatorOverland Park, KSProvide/coordinate the highest level of contact, counseling and support services Coordinate study activities and patient care with medical staff Implement and adhere to study protocol Perform Phlebotomy and IV procedures Prepare laboratory specimens for analysis, monitoring tests and procedures, shipping frozen specimen Execute medical orders within parameters of education, training and licensure Conduct study activities helping to ensure all safety parameters Maintain patient records in EMR and appropriate hospital records Assess and report adverse study events, including the IRB and any research sponsors Complete all paperwork affiliated with the study, including but not limited to the requirements of the facility, the IRB and the study Sponsor. Assess each proposed study protocol Facilitate administrative review and approval of proposed studies Develop tactical study procedures Develop any necessary study documents not provided by sponsor or IRB Educate HCA staff regarding research and study protocols Screen and recruit patients based on protocol criteria Explain study protocols, procedures and treatments to patients and families Conduct the Informed Consent process in conjunction with study investigators Ensure that an original copy of any subjects Informed Consent Document is the in the research binders, as well as, a copy on the subject's medical record.
Clinical Research Coordinator IV - Allergy Department Cincinnati Children's Hospital Medical CenterClinical Research Coordinator IV - Allergy DepartmentCincinnati, OH$61,401.60–$78,291.20 / yearCreate case report forms (CRFs) in consultation with other team members, as needed, using existing study data information to promote efficient data collection and data entry. Study Conduct/ Clinical Research Practice - Serve as a resource for others for all aspects of conducting a clinical trial for complex and multi-center trials.