Sr Clinical Research Coordinator CAREERXCHANGE, Inc.Sr Clinical Research CoordinatorMiami, FL$32–$43 / hourThis role is responsible for coordinating all aspects of clinical research studies, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines while delivering exceptional patient care. Job Summary We are seeking an experienced Senior Clinical Research Coordinator to support a busy clinical research team during a 15-week contract assignment.
Clinical Research Coordinator II - Gastroenterology University of ChicagoClinical Research Coordinator II - GastroenterologyHyde Park, IL$60,000–$75,000 / yearAnalyzes, facilitates and participates in the daily activities of multiple moderately complex clinical trials and performs all aspects of clinical data management, including patient data retrieval, referring MD office records, preparing clinical research charts, and participation in program audits. Maintains accurate and complete records which may include, but are not limited to, signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), drug dispensing logs, and study related communication.
Senior Clinical Research Coordinator Orso HealthSenior Clinical Research CoordinatorEl Centro, CA$33–$40 / hourOversee the day-to-day operations of clinical trials at various sites, ensuring adherence to study protocols, regulatory compliance, and good clinical practice (GCP). Act as the primary point of contact between the sponsor, study sites, and internal teams, facilitating effective communication and resolution of any issues that arise.
Clinical Research Assistant Alcanza Clinical Research LLCClinical Research AssistantWoodstock, GAResponsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol: Assists with the basic screening of patients for study enrollment; Assists with patient follow-up visits; Documents in source clinic charts; Enters data in EDC and answers queries; Obtains vital signs and ECGs; May perform blood draws; Perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Request and track medical record requests; Enters data in EDC and answers queries; Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and. Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed; Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
Clinical Research Coordinator Lead Nuvance HealthClinical Research Coordinator LeadPoughkeepsie, NY$33.21–$61.68 / hourEvaluates trial protocols, manages the clinical research sites including, but not limited to acting as primary contact for clinical research sites for questions related to the protocol conduct protocol, regulatory document completion, study supplies, client scheduling, and electronic data capture. Our team of more than 15,000 caregivers delivers compassionate care through seven community hospitals, primary care and specialty practice locations, outpatient settings, home care services and telehealth visits.
Phlebotomist – Home Visits (Clinical Research, Per Diem) Hawthorne HealthPhlebotomist – Home Visits (Clinical Research, Per Diem)Rochester, Minnesota$150–$400 / yearThis position is ideal for phlebotomists who are comfortable working independently, traveling to patient homes, and providing a professional, patient-centered experience while supporting important clinical research. We are seeking a skilled and compassionate Mobile Clinical Research Phlebotomist to support clinical research studies by conducting in-home visits with study participants .
Clinical Research Coordinator- Phase II-III - Full-Time - Wolf River - Registered Nurse (RN) Preferred West Cancer CenterClinical Research Coordinator- Phase II-III - Full-Time - Wolf River - Registered Nurse (RN) PreferredGermantown, TNThe Clinical Research Coordinator plays a vital role in managing oncology patients participating in pharmaceutical-sponsored clinical trials. If you are a detail-oriented clinical research professional looking to make a difference in oncology care, apply today to become a Clinical Research Coordinator at West Cancer Center.
Salt Lake City, UT- Clinical Research Coordinator Actalent IncSalt Lake City, UT- Clinical Research CoordinatorSalt Lake City, UT$25–$35 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. You will play a key role in driving study enrollment, engaging directly with participants, and collaborating closely with research staff to ensure high-quality data collection and protocol adherence.
Senior Clinical Research Associate IRESenior Clinical Research AssociateRemoteAs a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Bachelor's degree, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role.
Clinical Research Coordinator III Cincinnati Children’s HospitalClinical Research Coordinator IIIServe as CCHMC liaison to internal departments, clinical teams, regulatory agencies, physician's offices, city clinics, government agencies, academic centers, and other organizations. Recruitment/Enrollment/Retention - Determine best method/s to identify potential participants for research protocol (advertisements, chart reviews, monitoring of clinic schedule, etc.) and prepare accordingly.
NewCall Center Representative - Clinical Research Actalent IncCall Center Representative - Clinical ResearchRichardson, TXWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The specialist collaborates closely with clinical coordinators and the leadership team to meet recruitment goals and support the success of multiple clinical research protocols.
NewClinical Research Coordinator Level 1 IREClinical Research Coordinator Level 1Downers Grove, IllinoisPerforming technical and clinical requirements of study protocols, i.e., venipuncture, specimen processing, vital signs, electrocardiograms, IV infusions, IV pump operations, Holtor monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, injections (IM or SQ) or any procedure necessary for the protocol as ordered by the investigator. Obtaining and maintaining knowledge in regards to temperature monitoring devices and procedures for lab specimens and investigational products and providing detailed information to all staff and sponsors in regards to how temperatures are monitored and maintained.
Associate Director, Clinical Research BraccoAssociate Director, Clinical ResearchPrinceton, FloridaThis person has the responsibility to guide and supervise clinical research activities performed by external vendors (CROs), consultant monitors (when applicable) and clinical study assistants working on assigned projects. The Associate Director/ Director, Clinical Research is person is responsible for leading clinical research activities for a specific program or programs as well as managing all activities associated with performing one or more clinical studies.
Clinical Research Coordinator III - Pediatrics The Henry M Jackson Foundation for the Advancement of Military Medicine IncClinical Research Coordinator III - PediatricsBethesda, MDServes as the clinical and operational lead for assigned studies, leveraging clinical research expertise to guide and oversee protocol-specific clinical procedures, including participant assessments, specimen collection (e.g., pediatric blood draws), and administration of study interventions such as vaccines. Rare after-hours phone availability may be required to serve as a point of contact for emergency participant needs and to coordinate with the Principal Investigator and other study team members regarding serious adverse event (SAE) assessment and reporting, or any other urgent participant-related matters.
Clinical Research Physician (Cardiology or Metabolic) K2 Medical ResearchClinical Research Physician (Cardiology or Metabolic)Maitland, FLFull timeOur clinical trials experience/therapeutic areas include neurodegenerative disorders (Alzheimer’s, Parkinson’s, LBD), general medicine (Obesity, GLP-1 use, OA, HTN, DM, NASH/MASH and cardiometabolic) and some psychiatry as well. We have taken part in clinical trials for all current FDA-approved therapies that slow the progression of Alzheimer’s disease (AD) and most diagnostics (PET tracers, CSF and blood biomarkers) for the diagnosis of AD.
Exercise Physiologist Fountain LifeExercise PhysiologistHouston, TexasReview full-body DEXA scan results with members, including total and regional lean mass, fat mass, appendicular lean mass index, visceral adipose tissue, and bone mineral density, and translate these results into a training plan that protects bone, builds muscle, and reduces visceral fat. The Clinical Exercise Physiologist builds, delivers, and iterates on evidence-based aerobic, resistance, and mobility programming for every APEX member, partners directly with physicians on care planning, and serves as the clinical exercise subject matter expert for the Houston site.
Cardiac Rehab Clinician - (RN-BSN, RRT, PT or Exercise Physiologist) Community Hospital CorporationCardiac Rehab Clinician - (RN-BSN, RRT, PT or Exercise Physiologist)Gainesville, TexasThe Cardiac Rehab Clinician tracks patient progress through detailed reports and maintains critical communication with the Cardiac Rehabilitation Medical Director and primary physicians regarding clinical changes. This role is responsible for assessing patient needs, performing fitness tests, and developing customized exercise programs to improve mobility and aid recovery from injury, illness, or cardiovascular events.
NewClinical Research Nurse, Clinical Trials Office, Clinical Operations Virginia Commonwealth UniversityClinical Research Nurse, Clinical Trials Office, Clinical OperationsRichmond, VACandidates whose resumes highlight the following previous experience will be prioritized: Demonstrated experience working in and fostering an environment of respect, professionalism and civility with a population of faculty, staff, and students from various backgrounds and experiences, or a commitment to do so as a staff member at VCU; Advanced proficiency with data entry and word processing skills, with the ability to analyze and interpret information effectively; Advanced organizational abilities and a keen eye for detail to ensure accuracy and efficiency in all tasks with the ability to multitask and prioritize autonomously; Clear and professional written and verbal communication skills, with the ability to interact effectively with colleagues and stakeholders; Interpersonal skills, capable of building relationships and collaborating with team members at all levels to gather information and support compliance efforts; Problem-solving and organizational aptitude, with the ability to manage multiple tasks, meet deadlines in a dynamic environment and independently make critical decisions. certifications, seminars, courses, annual conferences, mentorship; 28 Vacation Days, 12+ State Holidays, and 4 Days to volunteer; Medical, Dental and Vision Health Benefits to meet the needs of employees and their eligible family members from the Commonwealth of Virginia as well as optional FSA; Participation in the Virginia Retirement System (VRS) and other retirement saving options; Parental and Caregiver Leave, Short Term Disability (STD), Disability Insurance, Voluntary Long Term Care Insurance, and Employee Assistance Program.
Associate Director of Clinical Research (IIT & Program Strategy Focus) - Radiation Oncology Washington University in St LouisAssociate Director of Clinical Research (IIT & Program Strategy Focus) - Radiation OncologySt. Louis, MO$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. Foster strong, collaborative relationships with key institutional partners across Washington University and BJC HealthCare (e.g., CTMS offices, Biorepositories, Research Administration, and hospital/laboratory groups) to streamline workflows and overcome institutional bottlenecks.
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.