NewClinical Research Coordinator JobotClinical Research CoordinatorFountain Valley, CA$35–$38 / hourThis individual will help facilitate patient appointments, coordinate procedures and diagnostic testing, ensure accurate documentation, maintain communication with patients and providers, and support research-related initiatives in accordance with established protocols and regulatory requirements. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.
R&D Manager, Clinical Research MedlineR&D Manager, Clinical ResearchNorthfield, IL$134,000–$201,000 / yearHiring staff, recommending pay increases, performing performance reviews, training and development of staff, estimating personnel needs, assigning work, meeting completion dates, interpreting and ensuring consistent application of organizational policies. This role oversees internal product evaluations, clinical studies, and customer-partnered quality improvement initiatives to ensure timely, compliant, and high-quality outcomes.
NewClinical Research Coordinator II CYNET SYSTEMSClinical Research Coordinator IISomerset, NJ$23–$28 / hourTemporaryContractorPart timeProvide clinical research support to investigators to prepare for and execute assigned research studies, including reviewing study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data. We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and professional staffing, powered by a high-performing recruitment engine operating across North America and Asia.
NewClinical Research Coordinator JouléClinical Research CoordinatorKenmore, NY$26–$30 / hourProficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred. Join a growing clinical research team as a Clinical Research Coordinator supporting clinical trials in Buffalo, NY.
NewClinical Research Associate 3 - Contract TalentBurst, Inc.Clinical Research Associate 3 - ContractDurham, NC$50.02–$62.53 / hourThe Clinical Research Associate (CRA) serves as a sponsor-side clinical operations representative responsible for oversight of investigational sites and support of high-quality study execution across Phase 1 oncology trials (required) plus other therapeutic areas monitoring oversight a plus. This role combines traditional site monitoring responsibilities with broader sponsor oversight activities, including identification of operational and quality risks, collaboration with CRO partners and vendors, and proactive escalation of issues that may affect subject safety, data integrity, protocol compliance, or study timelines.
NewPer Diem / PRN Nurse RN - Research / Clinical Research - $40 per hour CommonSpirit Health at HomePer Diem / PRN Nurse RN - Research / Clinical Research - $40 per hourCincinnati, OHLocated in Loveland, OH, CommonSpirit Health at Home has 83 sites of care across 15 states (Arkansas, Arizona, California, Colorado, Illinois, Indiana, Kentucky, Minnesota, Nebraska, North Dakota, Ohio, Oregon, Tennessee, Texas and Washington) and nearly 3,000 employees who support our mission by creating and nurturing healthy communities across the nation. CommonSpirit Health at Home is committed to delivering the best quality care and comprehensive home-based services to the communities we serve by offering quality care and services; home health, hospice care, palliative care, home infusion therapy and supplemental staffing.
Clinical Research Coordinator (oncology) CollaberaClinical Research Coordinator (oncology)Stanford$40–$51 / hourTemporaryContractorRequirements: Bachelor's degree in a related field and two years of experience in clinical research, or an equivalent combination of education and relevant experience. Cancer treatment trail experience, hospital/clinic coordinator experience, Phase 1 treatment trials, EPIC EMR skills.
Clinical Research Coordinator I (PA/NJ Residents Only) St. Luke's Health Network, Inc.Clinical Research Coordinator I (PA/NJ Residents Only)Bethlehem, PAFull timeIndividually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care. Bachelor’s degree required; will accept Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience highly preferred.
Clinical Research Coordinator I (PA/NJ residents only) St. Luke's Health Network, Inc.Clinical Research Coordinator I (PA/NJ residents only)Bethlehem, PAFull timeIndividually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care. Bachelor’s degree required; will accept Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience highly preferred.
Sr. Clinical Ethicist, Bioethics Program, Baptist Health Baptist HealthSr. Clinical Ethicist, Bioethics Program, Baptist HealthIn addition to responding to requests for ethics consultations, the senior clinical ethicist will engage in preventative ethics activities, including but not limited to participating in monthly Bioethics Performance Improvement Case Conferences, rounding on units throughout the Health System, partnering with Ethics Liaisons and Ethics Program colleagues to provide moral distress debriefs across the Health System, and offering guidance on clinical and organizational ethics issues as identified across the Health System. Working closely with other members of the Ethics Program, the senior clinical ethicist will share responsibility for receiving requests and conducting ethics consultations independently, documenting consultations in a timely and thorough manner in the electronic health record, and following up with patient cases after referral.
Clinical Ethicist, Bioethics Program, Baptist Health Baptist HealthClinical Ethicist, Bioethics Program, Baptist HealthIn addition to responding to requests for ethics consultations, the clinical ethicist will engage in preventative ethics activities, including but not limited to participating in monthly Bioethics Performance Improvement Case Conferences, rounding on units throughout the Health System, partnering with Ethics Liaisons and Ethics Program colleagues to provide moral distress debriefs across the Health System, and offering guidance on clinical and organizational ethics issues as identified across the Health System. Working closely with other members of the Ethics Program, the clinical ethicist will share responsibility for receiving requests and conducting ethics consultations independently, documenting consultations in a timely and thorough manner in the electronic health record, and following up with patient cases after referral.
NewClinical Ethicist, Bioethics Program, Baptist Health Baptist Health System IncClinical Ethicist, Bioethics Program, Baptist HealthJacksonville, FLIn addition to responding to requests for ethics consultations, the clinical ethicist will engage in preventative ethics activities, including but not limited to participating in monthly Bioethics Performance Improvement Case Conferences, rounding on units throughout the Health System, partnering with Ethics Liaisons and Ethics Program colleagues to provide moral distress debriefs across the Health System, and offering guidance on clinical and organizational ethics issues as identified across the Health System. Working closely with other members of the Ethics Program, the clinical ethicist will share responsibility for receiving requests and conducting ethics consultations independently, documenting consultations in a timely and thorough manner in the electronic health record, and following up with patient cases after referral.
NewSr. Clinical Ethicist, Bioethics Program, Baptist Health Baptist Health System IncSr. Clinical Ethicist, Bioethics Program, Baptist HealthJacksonville, FLIn addition to responding to requests for ethics consultations, the senior clinical ethicist will engage in preventative ethics activities, including but not limited to participating in monthly Bioethics Performance Improvement Case Conferences, rounding on units throughout the Health System, partnering with Ethics Liaisons and Ethics Program colleagues to provide moral distress debriefs across the Health System, and offering guidance on clinical and organizational ethics issues as identified across the Health System. Working closely with other members of the Ethics Program, the senior clinical ethicist will share responsibility for receiving requests and conducting ethics consultations independently, documenting consultations in a timely and thorough manner in the electronic health record, and following up with patient cases after referral.
Clinical Ethicist Part Time Days 8a-4p Atlantic Health Chilton Medical Center Atlantic Health System IncClinical Ethicist Part Time Days 8a-4p Atlantic Health Chilton Medical CenterPompton Plains, NJConsultations address ethically complex issues in patient care, including decision‑making capacity, informed consent and refusal, surrogate decision‑making, goals of care, end‑of‑life care, potentially inappropriate treatment, and value‑based conflict. We were awarded the American Heart Association/American Stroke Association's Get With The Guidelines-Stroke Gold Plus Quality Achievement Award with Target: Stroke Honor Roll Elite.
Clinical Ethicist Boston Children's HospitalClinical EthicistBoston, MA$49,576.80–$79,315.60 / yearThe Clinical Ethicist provides formal and informal ethics consultations and participates in clinical ethics rounds while collaborating with clinical teams, patients, and families to address ethical issues in pediatric health care and research. The role develops ethics resources and educational initiatives for the Boston Children's Hospital community, participates in hospital policy development and review related to ethical considerations, and serves as a facilitator for strengthening moral responsibility and ethical culture across the organization.
Senior Clinical Ethicist Northside Hospital Inc.Senior Clinical EthicistAtlanta, GeorgiaPer diemExperience of performing/leading complex ethics case consultation of all age populations (neonates to elderly) at the request of multiple disciplines; including experience with requesting court appointed guardianship for patients, consultations involving federally protected populations and de-escalation of conflicts among patients, family members and staff. Doctoral degree (PhD preferred) in bioethics, clinical ethics, nursing, healthcare or healthcare related field preferred; or, Doctor of Jurisprudence (JD).
Clinical Ethicist Banner HealthClinical EthicistConsultation services will identify and analyze the nature of uncertainty or conflict and facilitate resolution of conflicts with attention to interests, responsibilities and rights of all involved. 2. Provides education for stakeholders, physicians, nurses, patients, and other members of the medical staff related to program services.
Clinical Research Coordinator - Tumor Institute Providence St. Joseph HealthClinical Research Coordinator - Tumor InstituteSeattle, WAFull timeTogether, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.
Clinical Research Assistant II MultiCare Health SystemClinical Research Assistant IITacoma, WAFull timeMinimum two (2) years of related experience in healthcare or research (bench research, clinical research or health services research) OR one (1) year of healthcare experience plus one year of industry related research experience within a healthcare setting (such as working for MIRI). If your purpose and passions align with ours, you'll find a place to grow, do meaningful work and build a career you love in a community that feels like home.
Clinical Research Coordinator - Neuroscience Research Providence St. Joseph HealthClinical Research Coordinator - Neuroscience ResearchSeattle, WAFull timeIt is comprised of eight hospital campuses (Ballard, Edmonds, Everett, Centralia, Cherry Hill (Seattle), First Hill (Seattle), Issaquah and Olympia); emergency rooms and specialty centers in Redmond (East King County) and the Mill Creek area in Everett; and Providence Swedish Medical Group, a network of 190+ primary care and specialty care locations throughout the Puget Sound. Together, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington.
Regional Ethicist NEW Indiana University Health IncRegional Ethicist NEWCarmel, INIU Health, in partnership with the Indiana University School of Medicine, bring together highly skilled physicians, researchers, and educators into close collaboration to provide world-class care for children and adults and improve the health of patients and communities across Indiana. As one of Indiana's largest employers and the most comprehensive medical system in the state, our vision is to lead the transformation of healthcare through quality, innovation and education, and make Indiana one of the nation's healthiest states.
Clinical Research Coordinator I (Temporary/Part-Time) InBios International, Inc.Clinical Research Coordinator I (Temporary/Part-Time)Seattle, WA$26.44–$31.25 / hourPart timeThe successful candidate must have a BS in a scientific discipline, have familiarity with Good Clinical Practice (GCP) and have excellent attention to details as well as good communication skills but written and verbal. Monitor clinical study to ensure that all participant records entered into the electronic data capture system are accurate and follow the clinical protocol and source documents.
Ethicist OSF HealthCareEthicistPEORIA, Illinois$48.13–$56.63 / hourFull timeOSF HealthCare is dedicated to provide Mission Partners with a comprehensive and market-competitive total rewards package that includes benefits, compensation, recognition and well-being offerings that focus on the whole person and engage with their current stage of life and career. Demonstrated understanding and ability to apply, as well as competently teach, the Ethical and Religious Directives for Catholic Health Care Services as well as other key source texts relative to the Catholic Healthcare Ministry.
Clinical Research Associate II or Clinical Research Associate II RN - Bioethics Program St. Jude Children's Research Hospital IncClinical Research Associate II or Clinical Research Associate II RN - Bioethics ProgramMemphis, TN$70,720–$126,880 / yearThe program is led by two core faculty - Dr. Liza-Marie Johnson, whose scholarship focuses on clinical and research ethics with particular emphasis on informed consent, patient-provider communication, and the ethics of novel interventions - and Dr. Meaghann Weaver, whose work spans bioethics, palliative care, quality of life, and end-of-life decision-making for seriously ill children. Research themes across the program include ethical issues in pediatric genomic sequencing, communication and decision-making with seriously ill children and their families, the allocation of emerging therapies, and the experience of suffering and end-of-life care in pediatric populations.
(Temporary) Clinical Research Coordinator Certificate Trainee - WV Clinical & Translational Science Institute West Virginia University(Temporary) Clinical Research Coordinator Certificate Trainee - WV Clinical & Translational Science InstituteMorgantown, WVJun 23, 2026'',''Jun 23, 2026'',''Temporary'',''Temporary'',''Non-Exempt'',''Non-Exempt'',''No'',''No'',''Part-time'',''Part-time'',''false'',''378852'',''378852'',''true'',''378852'',''false'',''Submission for the position: (Temporary) Clinical Research Coordinator Certificate Trainee - WV Clinical & Translational Science Institute - (Job Number: 29717)'',''false'',''378852'',''false'',''true''. Management of Clinical Trial Patients: Involves a variety of resources and strategies to manage the care of patients participating in clinical trials, ensuring compliance with protocol procedures, assessments, and reporting requirements as well as management of symptoms.
(Hybrid) Clinical Research Coordinator III- Clinical and Translational Science Institute West Virginia University(Hybrid) Clinical Research Coordinator III- Clinical and Translational Science InstituteMorgantown, WVJun 30, 2026'',''Jun 30, 2026'',''Non-Classified'',''Non-Classified'',''Exempt'',''Exempt'',''Yes'',''Yes'',''Full-time'',''Full-time'',''false'',''379234'',''379234'',''true'',''379234'',''false'',''Submission for the position: (Hybrid) Clinical Research Coordinator III- Clinical and Translational Science Institute - (Job Number: 29777)'',''false'',''379234'',''false'',''true''. From the groundbreaking R1 research at our flagship campus in Morgantown to the career-oriented programs at WVU Potomac State in Keyser, and the technology-intensive programs at WVU Tech in Beckley, the contributions of WVU employees resonate across the state, touching lives and shaping futures.
NewClinical Research Supervisor UCSF Medical CenterClinical Research SupervisorSan Francisco, CAThe incumbent may have central responsibility for ensuring IRB approval and compliance, contract generation, negotiation and approval, subject recruitment, appropriate study testing, and adequate enrollment of multicenter clinical studies, longitudinal cohort studies, local investigator-initiated studies, and biorepository efforts; exercise strong administration and management leadership of clinical research, strong research coordination, and may lead experienced personnel to ensure optimal systems for efficiency, compliance, safety, financial oversight, and contractual expertise in negotiations and execution, as well as create and implement quality improvement processes. Positions at this level may perform expert and efficient integration of multiple complex programmatic activities, applying a sophisticated medical knowledge base, substantial leadership skills, effectively working with a variety of people and organizations at UCSF (clinicians, investigators, clinical staff, administration, Committee on Human Research, human resources, contracts and grants) and elsewhere (industry sponsors, coordinating centers, FDA, NIH), exhibiting an in-depth knowledge of specific programs.
Clinical Research Coordinator Temple UniversityClinical Research CoordinatorPhiladelphia, PA$50,000–$55,000 / yearPennsylvania-Philadelphia-Health Sciences Campus (HSC)-Kresge Science Hall'',''Pennsylvania-Philadelphia-Health Sciences Campus (HSC)-Kresge Science Hall'','''','''',''Staff'',''Staff'',''Full-time'',''Full-time'',''Day Job'',''Day Job'',''Regular'',''Regular'',''false'',''522097'',''522097'',''true'',''522097'',''false'',''Submission for the position: Clinical Research Coordinator - (Job Number: 26001626)'',''false'',''522097'',''false'',''true''. Position Summary: The Clinical Research Coordinator works under the leadership of the Principal Investigator and/or other Research Staff and is responsible for specific research tasks associated with clinical research projects or clinical trials, ensuring high-quality data collection, regulatory compliance, and seamless study operations.
Clinical Research Assistant-Recruitment Temple UniversityClinical Research Assistant-RecruitmentPhiladelphia, PAPennsylvania-Philadelphia-Health Sciences Campus (HSC)-Kresge Science Hall'',''Pennsylvania-Philadelphia-Health Sciences Campus (HSC)-Kresge Science Hall'','''','''',''Staff'',''Staff'',''Full-time'',''Full-time'',''Day Job'',''Day Job'',''Regular'',''Regular'',''false'',''521508'',''521508'',''true'',''521508'',''false'',''Submission for the position: Clinical Research Assistant-Recruitment - (Job Number: 26001407)'',''false'',''521508'',''false'',''true''. ''521508'',''true'',''521508'',''false'',''Submission for the position: Clinical Research Assistant-Recruitment - (Job Number: 26001407)'',''false'',''521508'',''false'',''true'',''Clinical Research Assistant-Recruitment'',''26001407'',''!*!
Clinical Research Senior Assistant OR Specialist University of Maryland School of MedicineClinical Research Senior Assistant OR SpecialistBaltimore, MD$59,000–$62,000 / yearThe Bone Marrow Transplant and Cellular Therapy (BMT-CT) research team within the Clinical Research Management Office of the University of Maryland, Baltimore School of Medicine, Marlene and Stewart Greenebaum Comprehensive Cancer Center (UMGCCC) is currently recruiting for a full-time Bone Marrow Senior Clinical Research Assistant or Clinical Research Specialist (Senior Clinical Research Assistant or Clinical Research Specialist). Provides training to less experienced researchers; assisting in developing and submitting grants, papers, abstracts, manuscripts and presenting studies; developing protocol manuals and data collection instruments; participating in field visits, responding to requests and questions from individuals, institutions, government agencies, and funding agencies; and participating in the design of research studies.
Clinical Research Manager UCSF Medical CenterClinical Research ManagerSan Francisco, CAThe Clinical Research Manager will work closely with senior management, including Principal Investigators, the Program Director, and Department leadership, to develop long and short term strategies to carryout the goal of developing effective treatments for Alzheimer's Disease, Progressive Supranuclear Palsy, Frontotemporal Dementia and other related disorders. To further engage in this work, the center collaborates with organizations such as the Alzheimer's Disease Research Center (ADRC), Bluefield Project to Cure Frontotemporal Dementia, California Alzheimer's Disease Center, Global Brain Health Institute, and the Tau Consortium.
Regulatory Clinical Research Coordinator (CRC), Licensed or Non-Licensed, varying levels University of VirginiaRegulatory Clinical Research Coordinator (CRC), Licensed or Non-Licensed, varying levelsCharlottesville, VAThe Division of Cardiovascular Medicine (Interventional Cardiology) at the University of Virginias (UVA) School of Medicine, is currently seeking applicants for Clinical Research Coordinators (CRC), Licensed or Non-Licensed positions, at various skill and experience levels to join a dynamic growing team of clinical research professionals. This position is open to applicants who meet the requirements of Clinical Research Coordinator 2, 3 and 4. The CRC will work closely with physicians, research staff, sponsors, IRB and regulatory department staff.
NewClinical Research Coordinator, Varying Levels; Cardiovascular Medicine University of VirginiaClinical Research Coordinator, Varying Levels; Cardiovascular MedicineCharlottesville, VAThe Division of Cardiovascular Medicine (Interventional Cardiology) at the University of Virginia's (UVA) School of Medicine, is currently seeking applicants for Clinical Research Coordinators (CRC), Licensed or Non-Licensed positions, at various skill and experience levels to join a dynamic growing team of clinical research professionals. Research reference information: Innovating proctoring with live/recorded surgical cases, spanning across departments: https://www.uvaphysicianresource.com/uva-structural-heart-disease-team-performs-live-cases-at-the-2021-international-tvt-conference/ .
Clinical Research Coordinator III Tulane UniversityClinical Research Coordinator IIINew Orleans, LAThe Clinical Research Coordinator III screens, enrolls and follows study patients, ensuring protocol compliance and close patient monitoring, and works independently in designing, coordinating, and implementing all assigned research projects. Legally protected demographic classifications (such as a person's race, color, religion, age, sex, national origin, shared ancestry, disability, genetics, veteran status, or any other characteristic protected by federal, state, or local laws) are not relied upon as an eligibility, selection or participation criteria for Tulane's employment or educational programs or activities.
NewSenior Clinical Research Monitor Integrated Resources, IncSenior Clinical Research MonitorMounds View, MinnesotaFull timeThis position works under minimal supervision, working closely with study teams, site personnel, and Healthcare field personnel and monitoring supervisor for resolution of site issues.· general therapeutic area education and training)Physical Job Requirements• The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job.
Clinical Research Administrator - Pediatrics TMC University of Texas Health Science Center at HoustonClinical Research Administrator - Pediatrics TMCHouston, TXCertification/Skills: NoneMinimum Education:Bachelor''s Degree in Healthcare Administration, Business, Finance, Accounting, or related degree requiredMinimum Experience:3 years of related experience requiredPhysical Requirements:Exerts up to 20 pounds of force occasionally and/or up to 10 pounds frequently and/or a negligible amount constantly to move objects. Our total rewards package includes the benefits you'd expect from a top healthcare organization (benefits, insurance, etc.), plus: 100% paid medical premiums for our full-time employees Generous time off (holidays, preventative leave day, both vacation and sick time - all of which equates to around 37-38 days per year) The longer you stay, the more vacation you'll accrue!
Sr. Clinical Research Nurse - Transplant Center Houston MethodistSr. Clinical Research Nurse - Transplant CenterTexasAssists Principal Investigator to ensure that all persons ‘engaged’ in research studies have met training requirements in accordance with Federal regulations and entity policies and procedures including preparing Institutional Review Board (IRB) and regulatory documents following ICH/GCP guidelines, and the development of materials and tools necessary to appropriately facilitate the conduct of research. Leads initiatives to improve quality and safety scores, through peer-to-peer accountability Performs nursing functions independently while following the clinical research protocol and nursing process which would include, modification of care based on continuous evaluation of the research patient’s condition.
Regulatory Clinical Research Coordinator (CRC), Licensed or Non-Licensed, varying levels Commonwealth of VirginiaRegulatory Clinical Research Coordinator (CRC), Licensed or Non-Licensed, varying levelsCharlottesville, VAThe Division of Cardiovascular Medicine (Interventional Cardiology) at the University of Virginias (UVA) School of Medicine, is currently seeking applicants for Clinical Research Coordinators (CRC), Licensed or Non-Licensed positions, at various skill and experience levels to join a dynamic growing team of clinical research professionals. This position is open to applicants who meet the requirements of Clinical Research Coordinator 2, 3 and 4. The CRC will work closely with physicians, research staff, sponsors, IRB and regulatory department staff.
NewClinical Research Coordinator, Varying Levels; Cardiovascular Medicine Commonwealth of VirginiaClinical Research Coordinator, Varying Levels; Cardiovascular MedicineCharlottesville, VAThe Division of Cardiovascular Medicine (Interventional Cardiology) at the University of Virginia's (UVA) School of Medicine, is currently seeking applicants for Clinical Research Coordinators (CRC), Licensed or Non-Licensed positions, at various skill and experience levels to join a dynamic growing team of clinical research professionals. Research reference information: Innovating proctoring with live/recorded surgical cases, spanning across departments: https://www.uvaphysicianresource.com/uva-structural-heart-disease-team-performs-live-cases-at-the-2021-international-tvt-conference/ .
Clinical Research Nurse Texas Tech UniversityClinical Research NurseLubbock, TXThe Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act is a federal statute requiring colleges and universities participating in federal financial aid programs to maintain and disclose campus crime statistics and security information. Team members also enjoy a variety of other perks, such as special membership rates at local gyms and golf courses, access to state-of-the-art software and facilities, and discounts on travel, technology, entertainment and more.
Clinical Research Coord Associate Technician Assistant University of MichiganClinical Research Coord Associate Technician AssistantAnn Arbor, MIMinimum 1 year directly related experience in clinical research and clinical trials is necessary or an advanced degree in a health-related area such as Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD or minimum 3 years of human subject experience (clinical, lab, or health regulations) such as related patient care, related community health and wellness, related clinical information, and research. This position will serve as a Clinical Research Coordinator Associate in the Oncology Clinical Trial Support Unit (O-CTSU) providing administrative study coordination and data entry support to faculty and research teams for the University of Michigan Rogel Cancer Center - an NCI-Designated Comprehensive Cancer Center and a member of the National Comprehensive Cancer Network (NCCN).
Clinical Research Finance & CTMS Specialist Gastro HealthClinical Research Finance & CTMS SpecialistBirmingham, ALPartner with site staff to ensure completed visits, procedures, stipends, screen failures, unscheduled visits, and protocolrequired activities are properly documented and financially captured. This role will report to the Finance Department, while working closely with Clinical Research leadership, site managers, coordinators, investigators, sponsors, CROs, and external financial partners.
Associate Director Clinical Research (Hybrid) - Psychiatry Washington University in St LouisAssociate Director Clinical Research (Hybrid) - PsychiatryMO$84,200–$148,500 / yearCertifications/Professional Licenses: Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals (ACRP), Certified Clinical Research Professional (CCRP) - Society of Clinical Research Associates (SOCRA), Clinical Research Associate (CRA) - Association of Clinical Research Professionals (ACRP), Clinical Research Management (CRM) - Association of Clinical Research Professionals (ACRP), Clinical Research Professional (CRP) - Association of Clinical Research Professionals (ACRP), Registered Nurse - Illinois Department of Financial and Professional Regulation, Registered Nurse - Missouri Division of Professional Registration. This initiative requires the employee to partner with departmental leadership, investigators, clinical operations, informatics/EPIC teams, HRPO, OVCR, the Research Contracts Office, and other institutional stakeholders to develop protocols, workflows, governance processes, reporting structures, and quality controls that support compliant and sustainable implementation.
NewClinical Research Coordinator - Raleigh, NC IQVIAClinical Research Coordinator - Raleigh, NCParsippany, North CarolinaThe ideal candidate has hands-on clinical research experience, is comfortable performing study-related procedures, and possesses strong organizational skills in both data management and regulatory documentation. Experience supporting regulatory processes , including electronic regulatory filing, document maintenance, and ensuring study documentation complies with sponsor and regulatory requirements.
Clinical Research HRPP Program Specialist University of ToledoClinical Research HRPP Program SpecialistToledo, OHThis position provides expert advice to principal investigators (PIs), Clinical Research Coordinators, leadership and other ORSP personnel involved in ensuring compliance throughout the lifecycle of clinical research and trials. With the exception of positions within University of Toledo Main Campus and the University of Toledo College of Medicine and Life Sciences, the employment offer is conditional upon successful completion of a cotinine test and Occupational Health clearance.
NewClinical Research Coord I Main Line Health SystemClinical Research Coord IWynnewood, PA$50,793.60–$78,707.20 / yearDaily tasks are conducted on site at the Main Line Health Hospitals and may include the oversight and coordination of a variety of clinical studies, executing study procedures as outlined by the study protocol (and related documents). Just as each of our patients requires a personalized care plan, each of our employees, physicians, and volunteers, bring distinctive talents to Main Line Health.
Clinical Research Monitor II Temple University Health SystemClinical Research Monitor IIPhiladelphia, PA404810'',''true'',''404810'',''false'',''Submission for the position: Clinical Research Monitor II - (Job Number: 263138)'',''false'',''404810'',''false'',''true'',''Clinical Research Monitor II'',''263138'',''!*!The OCR Clinical Research Monitor II, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial research both from a documentation and process level. '',''Pennsylvania-Philadelphia'',''Pennsylvania-Philadelphia'',''Research & Science'',''Research & Science'',''Full-time'',''Full-time'',''Day Job'',''Day Job'',''Regular'',''Regular'',''false'',''404810'',''404810'',''true'',''404810'',''false'',''Submission for the position: Clinical Research Monitor II - (Job Number: 263138)'',''false'',''404810'',''false'',''true''.
NewClinical Research Coordinator Hackensack Meridian HealthClinical Research CoordinatorHackensack, New JerseyFull timeSchedules, coordinates, prepares, and assists for all sponsor monitor site visits and ensures all supporting documentation records are adequate and available for the visit; Meets with monitor at least once during each monitor site visit and resolves all issues found during visit. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.
CLINICAL RESEARCH NURSE COORDINATOR III (4) University of Alabama at BirminghamCLINICAL RESEARCH NURSE COORDINATOR III (4)Birmingham, AL$67,070–$108,990 / yearUniversity'',''University'','''','''','''','''','''','''','''','''',''Clinical Research'',''Clinical Research'',''310008400 Comprehensive Cancer Center'',''310008400 Comprehensive Cancer Center'',''Regular'',''Regular'','''','''','''','''',''Day/1st Shift'',''Day/1st Shift'',''Onsite'',''Onsite'',''false'',''321597'',''321597'',''true'',''321597'',''false'',''Submission for the position: CLINICAL RESEARCH NURSE COORDINATOR III (4) - (Job Number: T236184)'',''false'',''321597'',''false'',''true''. The O''Neal Cancer Center powers more than 400 scientists and physician-scientists, cares for 20,000 patients annually, and is home to more than 160 employees, plus all the physicians and clinical staff engaged in cancer patient care.
Clinical Research Recruitment Specialist University of ColoradoClinical Research Recruitment SpecialistDenver, CO$46,116–$61,795 / yearUnder the direction of the Program Manager of the Clinical Research Recruitment Program, the Clinical Research Recruitment Specialist will be responsible for helping support the services and resources that the Clinical Research Recruitment Program offers the CU Anschutz Research Community including but not limited to recruitment consultations, social media campaigns for engaging people in clinical research, and education and training of clinical research teams on recruitment strategies and best practices. Help communicate with research teams regarding social media campaigns including confirming campaign parameters, sending campaign metrics, and obtaining enrollment numbers after campaigns end.