27039 clinical research coordinator jobs found

Job Description This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area. This exciting opportunity at a top medical center involves cutting-edge cancer research and requires strong skills in data entry, planning and scheduling, and computer literacy to support a dynamic and collaborative team. The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data,...

Job Description The top qualifications for success in this role include hands-on experience coordinating clinical research involving human subjects, including familiarity with IRB processes, informed consent, and direct or virtual patient engagement. Additionally, applicants should bring strong data analysis and management skills, ideally with experience working with clinical or digital health data, statistical software (e.g., R, Stata, SAS), and tools like REDCap. This is an exciting opportunity for medical students to contribute to innovative research at the intersection of digital health and cancer survivorship. Participants will gain meaningful experience through patient interaction, data-driven research, and collaborative scholarly activities—with opportunities to support abstract submissions, manuscripts, and interdisciplinary projects that advance the field. The Clinical Research Coordinator II works independently providing study coordination including screening of...

Job Description This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area. The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents information at regular research staff meetings. May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying...

Senior Clinical Research Coordinator HDF Comprehensive Cancer Center Full Time 85093BR Job Summary Senior Clinical Research Coordinators with the Pediatric Oncology program independently coordinate and are accountable for the overall administration of one or more clinical studies, typically requiring advanced level knowledge and skills. They may provide leadership to lower-level clinical research coordinators and/or other support personnel. The position is...

Job Description This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area. The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents information at regular research staff meetings. May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying...

Job Description The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and niche care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes. Are you ready to be a part of breakthrough research? The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the...

Assistant Clinical Research Coordinator Neurology Full Time 85100BR Job Summary The Assistant Clinical Research Coordinator (Assistant CRC) works directly with the Principal Investigator (PI) and performs duties related to the support and coordination of research. The Assistant CRC's primary duties include, but are not limited to, screening, enrollment, and tracking of research participants; preparation of experiment materials and protocols; data collection using a variety of...

Senior Clinical Research Coordinator HDF Comprehensive Cancer Center Full Time 85093BR Job Summary Senior Clinical Research Coordinators with the Pediatric Oncology program independently coordinate and are accountable for the overall administration of one or more clinical studies, typically requiring advanced level knowledge and skills. They may provide leadership to lower-level clinical research coordinators and/or other support personnel. The position is responsible for, and...

Join a team that delivers excellence. Lehigh Valley Health Network (LVHN) is home to nearly 23,000 colleagues who make up our talented, vibrant and diverse workforce. Join our team and experience firsthand what it's like to be part of a health care organization that's nationally recognized, forward-thinking and offers plenty of opportunity to do great work. Imagine a career at one of the nation's most advanced health networks. Be part of an exceptional health care experience. Join the inspired, passionate team at Lehigh Valley Health Network, a nationally recognized, forward-thinking organization offering plenty of opportunity to do great work. LVHN has been ranked among the "Best Hospitals" by U.S. News & World Report for 23 consecutive years. We're a Magnet(tm) Hospital, having been honored five times with the American Nurses Credentialing Center's prestigious distinction for nursing excellence and quality patient outcomes in our Lehigh Valley region. Finally,...

Job Description The Clinical Research Coordinator performs daily clinical research activities in accordance with approved protocols administered by the Clinical Trials Office within the Comprehensive Cancer Center at The Ohio State University Wexner Medical Center. Responsibilities Assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols Recruit, interview and enroll patients Obtain informed consent and ensure consent process is administered in compliance with regulatory and sponsor requirements Educate patients and families of purpose, goals, and processes of clinical study Coordinate scheduling and follow-through of patient care appointments, procedures, amp; other diagnostic testing in accordance with the study protocol Assist with monitoring patients for adverse reactions to study treatment, procedure, or medication and notifies appropriate clinical professionals to evaluate...

Job Description This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area. The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents information at regular research staff meetings. May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying...

Job Description Come join our team! The Clinical Research Coordinator III works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for oversight of all studies with the group and the assignment of studies to clinical research personnel within the group, and supervision of research staff. Plans and coordinates strategies for increasing patient enrollment, improving efficiency, training of personnel, and identifying new research opportunities. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). What are the Primary Duties & Responsibilities? Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients,...

Assistant Clinical Research Coordinator MED-CORE-HOSP Full Time 84626BR Job Summary The UCSF Airway Clinical Research Center (ACRC) integrates research programs in asthma, COPD, sarcoidosis, and cystic fibrosis, along with current programs sponsored by the National Institutes of Health and the pharmaceutical industry. Reporting to and under the direct supervision of the Research Manager, the incumbent will perform entry-level duties related to the support and...

LanceSoft is seeking a local contract Clinical Research Coordinator for a local contract job in Mission Viejo, California. Job Description & Requirements Specialty: Clinical Research Coordinator Discipline: Allied Health Professional Start Date: 07/07/2025 Duration: 13 weeks 39 hours per week Shift: 8 hours, days Employment Type: Local Contract ONCOLOGY OUTPATIENT CENTER HYBRID - 3 DAYS ONSITE, FLEXIBLE ON WHICH DAYS Shift: 5X8 0800-1600 Clinical Research Coordinator Experience Required Required Skills: Create and maintain study flows informed consent facilitation Maintain Accurate and Complete Subject Records Protocol Compliance Subject Enrollment Form IRB Compliance Principal Investigator Responsibilities Proficient EMR navigation   Preferred Skills: Experience in an ONC setting preferred Experience with Phase II and III preferred Experience with venipuncture/phleb preferred Experience with Patient Enrollment...

Job Description Grow your career at Cedars-Sinai! The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. Our board-certified fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists work closely together to advance cancer care. We are committed to bringing innovative therapeutic options to all of our patients with cancer! Join our team and contribute to groundbreaking research. We are seeking a dedicated Clinical Research Coordinator II to join our team. The ideal candidate will have a minimum of an Associate Degree or College Diploma and at least 3 years of clinical research coordination or related experience. A current Basic Life Support (BLS) Certification from the American Heart Association (AHA) – Healthcare Provider type...

Description The Department of Surgery is seeking a full time Clinical Research Coordinator to contribute to the overall operational management of clinical research / trial / study activities from design, set up, conduct, through closeout. In this position you will have responsibility for: The implementation of research activities for one or more studies. Recognizing and performing necessary tasks to manage projects and prioritizes work to meet necessary deadlines. Planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). The Clinical Research Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited...

Apply for Job Job ID 100237 Location Aurora Position Type Regular Regular/Temporary Regular Add to Favorite Jobs Email this Job Job Overview The Clinical Research Coordinator Associate is responsible for participating in the day-to-day operations of routine, minimally complex clinical research programs and/or studies conducted by Principal Investigators (PIs) at the University of Colorado Anschutz Medical Campus. Performs a variety of administrative and operational duties involved in the collection, compilation, documentation, and review of clinical research data. Supports the achievement of research program and/or study objectives. Works under close supervision, receiving instruction, guidance and direction from Senior CRC, Clinical Research Supervisor and/or leadership team. We are looking for a fun, motivated, and team-oriented person to join the Multidisciplinary 2.0 team,...

Description The West Virginia Clinical & Translational Science Institute (WVCTSI) at West Virginia University is currently accepting applications for a Temporary Clinical Research Coordinator Certificate Trainee. About the Opportunity As a Clinical Research Coordinator Certificate Trainee, you will be enrolled in the IDeA State Consortium for Clinical Research - Resource Center (ISOCRE-RC) Clinical Research Coordinator Development Program (CRCDP). Under the supervision of a preceptor, the trainee will complete 400 hours of experiential training and approximately 60 hours of self-paced didactic learning. This program is designed to provide trainees with the basic skills and knowledge to begin a career as a clinical research coordinator or specialist. The goal of the program is to build workforce capacity for clinical trials research. Under direct supervisions, trainees will participate in the development, coordination, and implementation of research...

Position Description: Clinical Research Coordinator III - GOOD Study Purpose Coordinate the day-to-day administrative activities of the clinical research trials program. Provide support to the team to facilitate the achievement of the program's goals. Recruit, train, and supervise staff and manage study budgets. Primary Functions * Oversee the recruitment, screening, enrolling and obtaining of consent from program participants. Conduct or coordinate training for program participants. * Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining contact with study participants. * Oversee the collection, analysis, and dissemination of research data. Report program data and progress to study investigators and program stakeholders including...

The Senior Clinical Research Coordinator is a leadership position focused on ALS clinical trials and studies only. The Sr. CRC serves as lead resource in the execution of assigned clinical research studies in accordance with approved protocols administered by the non-cancer Center for Clinical Research Management (CCRM) for the Division of Neuromuscular in the Department of Neurology; oversees, implements amp; coordinates conduct of daily activities of research studies; serves as primary reviewer of patient records to assess and identify patients who meet criteria for participation in research studies ; recruits, interviews and promotes study to eligible patients; educates patients and families of purpose, goals, and processes of clinical study; leads patient enrollment activities and ensures informed consent authorization is obtained amp; administered in compliance to regulatory amp; sponsor requirements; facilitates collection, processing amp; evaluation of...