2601 clinical research coordinator jobs found

Department Overview The Knight Cardiovascular Institute Clinical Senior Research Assistant (Research Coordinator) is responsible for various duties related to clinical trials. The research coordinator will Identify potential subjects through chart review, discussion with investigator or other mechanisms; assists PI in the identification and eligibility of new protocol subjects; schedules, orders, communicates assessments and appointments. They are responsible for trial implementation for all trials that fall under their specific discipline. The Research Coordinator is also the primary liaison for patients receiving experimental research procedures on a clinical trial and is responsible for the triage of patient needs and identification, reporting of, and follow-up of adverse events. They have a strong understanding of the connection and differences between clinical care and protocol visits conducted for research subjects. The research coordinator will have a very strong...

Department: Location: Health Sciences Center Time Type: Part time Worker Type: Temporary (Fixed Term) Job Req ID: R106247 Minimum Requirements: Four or more years of related experience or an equivalent combination of education and experience. Position Description: A Temporary Clinical Research Coordinator is needed to coordinate clinical research studies conducted at the Department of Surgery, Division of Surgical Oncology patients. Clinical Research at the Department of Surgery, Division of Surgical Oncology includes early phase, novel treatment, multi-centered, cooperative and intergroup trials, multi-institutional device, pharmaceutical trials, hepatic arterial studies, and single- or multi-centered investigator-initiated trials. This is a part time temporary position scheduled to work 15 hours per week. Essential Duties and Responsibilities: Facilitates compliance with the research protocol and Good Clinical Practice guidelines. Uses multiple...

Title: Clinical Research Coordinator I Job Type: Regular Company: Health Research, Inc. (HRI) Roswell Park Division Department: Pediatrics Time Type: Full time Weekly Hours: 40 FTE: 1 Shift: First Shift (United States of America) Summary: Manages and coordinates the care of patients participating in a pediatric clinical research study with guidance from preceptor, educator and/or administrator; educates patients, families and staff regarding study compliance; collects a complete and accurate study data set and facilitates accrual to clinical research studies. Maintains pediatric database through EHR abstraction. Position reports to Chair of Pediatrics The salary range for this position which includes an geographic differential is $70,887 - $88,793 annually and also includes a comprehensive benefits package. The listed pay range reflects the range of potential compensation for this role. The actual offer may vary based on qualifications, skills, and...

Clinical Research Coordinator (Contract Position) Duration : Open ended contract (average duration is 3-6 months) Job Type: Hours will fluctuate from 25-40 hours per week (Monday-Friday) - during normal business hours Start Date: ASAP Job Description We are seeking a full-time, onsite Clinical Research Coordinator (CRC) with experience in clinical research to support an ongoing Oncology clinical trial. The ideal candidate will be able to work independently and act as one of the main CRCs for this study. As the position and study progress, additional responsibilities may be assigned. The candidate must be flexible and willing to assist with various tasks as needed. Key Responsibilities Patient Recruitment: Identify and recruit suitable patients for the clinical trial. Medical Record Review: Conduct thorough reviews of patient medical records. Participant Screening: Perform phone screenings or prescreen participants for eligibility. Informed Consent: Obtain...

Department: Location: Health Sciences Center Time Type: Full time Worker Type: Regular Job Req ID: R106232 Minimum Requirements: Bachelor's degree in a related field and two (2) or more years of relevant research experience, or an equivalent combination of education and work experience. Grade 5E (Salary) Position Description: Working under the direction of the clinical Principal Investigators (PI), the Clinical Research Coordinator V is responsible for the enrollment, active accrual, implementation, facilitation and coordination of daily clinical trials activities and plays a critical role in the conduct of multiple clinical research studies. The Clinical Research Coordinator V works collaboratively with investigators, multidisciplinary clinical entities, sponsors, monitors and regulatory entities to ensure the safety of study participants, the efficiency of study operations and the timely completion of studies....

Department: Location: Health Sciences Center Time Type: Full time Worker Type: Regular Job Req ID: R106232 Minimum Requirements: Bachelor's degree in a related field and two (2) or more years of relevant research experience, or an equivalent combination of education and work experience. Grade 5E (Salary) Position Description: Working under the direction of the clinical Principal Investigators (PI), the Clinical Research Coordinator V is responsible for the enrollment, active accrual, implementation, facilitation and coordination of daily clinical trials activities and plays a critical role in the conduct of multiple clinical research studies. The Clinical Research Coordinator V works collaboratively with investigators, multidisciplinary clinical entities, sponsors, monitors and regulatory entities to ensure the safety of study participants, the efficiency of study operations and the timely completion of studies. The Clinical Research Coordinator V is also...

University of Colorado Anschutz Medical Campus Department: Cancer Center Working Title: Clinical Research Coordinator – Satellite Office in Cherry Creek Position #: 00708707 – Requisition #: 35859 Job Summary: The Cancer Center is looking to hire a full-time Clinical Research Coordinator (CRC) to work at our Satellite office in Cherry Creek. Key Responsibilities: Intermediate Level or CRC II, all the above and: Independently master study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies Independently perform study related processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies Assist Team Leads, Supervisors and/or management with creation and implementation of processes and procedures and quality improvement initiatives Act as a Primary Coordinator on multiple trials/studies Assist and train junior team members Senior...

Job Summary: The Clinical Research Coordinator will join the Clinical Research Central Office (CRCO) at the University of Wisconsin Carbone Cancer Center (UWCCC) to work on cancer clinical research within one or more Disease-Oriented Teams under the direction of a Clinical Team Manager. The UWCCC participates in Phase I, II and III oncology clinical research funded by national, federal and private sponsors. This position will interface with hospital personnel, inpatient and outpatient clinics and a referral network as necessary to identify, collect, and disseminate patient and protocol information. The selected candidate must demonstrate strong oral and written communication skills and an ability to work with patients and health care providers. The incumbent will work independently and as part of a group on multiple projects simultaneously, prioritizing projects based on deadlines and interdisciplinary collaboration. Attention to detail, time management and excellent...

Job Summary: The Clinical Research Coordinator will join the Clinical Research Central Office (CRCO) at the University of Wisconsin Carbone Cancer Center (UWCCC) to work on cancer clinical research within one or more Disease-Oriented Teams under the direction of a Clinical Team Manager. The UWCCC participates in Phase I, II and III oncology clinical research funded by national, federal and private sponsors. This position will interface with hospital personnel, inpatient and outpatient clinics and a referral network as necessary to identify, collect, and disseminate patient and protocol information. The selected candidate must demonstrate strong oral and written communication skills and an ability to work with patients and health care providers. The incumbent will work independently and as part of a group on multiple projects simultaneously, prioritizing projects based on deadlines and interdisciplinary collaboration. Attention to detail, time management and excellent...

University of Colorado Anschutz Medical Campus Department: Cancer Center Working Title: Clinical Research Coordinator – Gyn Team Position #: 734801 – Requisition #: 35872 Job Summary: The Cancer Center is looking to hire a full-time Clinical Research Coordinator (CRC) to work at our Aurora, CO location on the Gyn team. Key Responsibilities: Entry Level or CRC I: Assist with and oversee the day-to-day operations of clinical trials and studies Obtain study subject’s medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial Perform informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required Interview prospective subjects for a variety of research clinical trials. Educate potential subjects on the details of the studies through...

University of Colorado Anschutz Medical Campus Department: Cancer Center Working Title: Clinical Research Coordinator – Satellite Office in Cherry Creek Position #: 00708707 – Requisition #: 35859 Job Summary: The Cancer Center is looking to hire a full-time Clinical Research Coordinator (CRC) to work at our Satellite office in Cherry Creek. Key Responsibilities: Intermediate Level or CRC II, all the above and: Independently master study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies Independently perform study related processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies Assist Team Leads, Supervisors and/or management with creation and implementation of processes and procedures and quality improvement initiatives Act as a Primary Coordinator on multiple trials/studies Assist and train junior team...

Position Highlights The Clinical Research Coordinator II provides research support for the Department of Urology, working under the direction of a Principal Investigator, providing overall support and coordination of multiple research projects. This position will support the Department's research program which includes clinical research in kidney cancer, prostate cancer, kidney stones, female urology, as well as health disparities studies. The CRC II works closely with the principal investigator(s) and has a diverse set of duties ensuring that the study is run in compliance with the protocol and good clinical practices. This position will play an integral role in helping support the Department's academic mission of scholarly activity. Outstanding UA 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; retirement...

The Division of Cardiovascular Medicine, within Stanford University Department of Medicine, is a dynamic and innovative center dedicated to excellence in research, medical education, and clinical care. Our Division is driven by over 90 faculty members and a cadre of staff who are the pillar of strength in the Division's ongoing efforts into the prevention and treatment of cardiovascular disease. We are seeking a Clinical Research Coordinator 2 (CRC-2) who is passionate about clinical research and wants to deliver results. The CRC-2 will have the opportunity to work with a robust clinical research team, hand in hand with the Principal Investigators, Clinical Research Manager and other associates in support of the Interventional Affinity Group and the Structural Heart Research Program. The successful applicant will have the ability to supervise clinical research staff, collaborate with external vendors, and enjoy working in a dynamic work environment. Exceptional diplomacy,...

Position Highlights The Clinical Research Coordinator II provides research support for the Department of Urology, working under the direction of a Principal Investigator, providing overall support and coordination of multiple research projects. This position will support the Department's research program which includes clinical research in kidney cancer, prostate cancer, kidney stones, female urology, as well as health disparities studies. The CRC II works closely with the principal investigator(s) and has a diverse set of duties ensuring that the study is run in compliance with the protocol and good clinical practices. This position will play an integral role in helping support the Department's academic mission of scholarly activity. Outstanding UA 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; retirement...

Current University of Arkansas System employees, including student employees and graduate assistants, need to log in to Workday via MyApps.Microsoft.com , then access Find Jobs from the Workday search bar to view and apply for open positions. Students at University of Arkansas System two-year institutions will also view open positions and apply within Workday by searching for “Find Jobs for Students”. All Job Postings will close at 12:01 a.m. CT on the specified Closing Date (if designated). If you close the browser or exit your application prior to submitting, the application process will be saved as a draft. You will be able to access and complete the application through “My Draft Applications” located on your Candidate Home page. Closing Date: 02/06/2025 Type of Position: Researchers Job Type: Regular Work Shift: Sponsorship Available: No Institution Name: University of Arkansas for Medical Sciences The University of...

Oncology Clinical Research Coordinator (Contract Position) Contract Duration: Open ended contract (average duration is between 3-6 months) Job Type: Full-time 40 hours per week (Monday-Friday) - during normal business hours Start Date: ASAP Job Description We are seeking a full-time, onsite Clinical Research Coordinator with experience in clinical research to support an ongoing Oncology clinical trial. The ideal candidate will be able to work independently and act as one of the main CRC's for this study. As the position and study progress, additional responsibilities may be assigned. The candidate must be flexible and willing to assist with various tasks as needed. Key Responsibilities Data Management: Collect study data and enter it into electronic data capture (EDC) systems. Query Resolution : Address and resolve data queries promptly. General Support: Assist with any other study-related efforts as deemed necessary by the site. Qualifications...

Position: Clinical Research Coordinator II, Clinical Research Network Location: Boston, MA Schedule: 40 hours per week ABOUT BMC: At Boston Medical Center (BMC), our diverse staff works together for one goal — to provide exceptional and equitable care to improve the health of the people of Boston. Our bold vision to transform health care is powered by our respect for our patients and our commitment to ensure everyone who comes through our doors has a positive experience. You’ll find a supportive work environment at BMC, with rich opportunities throughout your career for training, development, and growth and where you’ll have the tools you need to take charge of your own practice environment. POSITION SUMMARY: The Clinical Research Coordinator II (CRC II) procures, processes and ships research specimens and conducts patient recruitment, administers questionnaires, abstracts medical records, maintains patient databases, enters data into...

Job Summary: Are you passionate about using research to positively impact quality of life and health outcomes? The research lab of Dr. Taylor House is hiring a Clinical Research Coordinator to coordinate research studies focused on enhancing communication between children with kidney disease and their medical teams to improve health outcomes. You will have the opportunity to be involved in daily research activities such as participant screening, recruiting, enrollment, and coordination, as well as broader strategic initiatives within the lab, including process development and building academic and community partnerships. The House Lab is part of the School of Medicine Department of Pediatrics, a vibrant, interdisciplinary, nationally recognized clinical and research academic department. Responsibilities: Clinical Research Coordinator I (RE015) Clinical Research Coordinator II (RE016) Institutional Statement on Diversity: Diversity is a source of strength,...

Job Title: Clinical Research Coordinator Job Description We are seeking an experienced Clinical Research Coordinator who will oversee the day-to-day activities of clinical trials in accordance with Good Clinical Research Practice (GCP). The role involves training and supervising research staff, ensuring regulatory compliance, maintaining accurate documentation, and managing data collection and storage. You will interact with co-workers, visitors, and other staff consistent with our values, ensuring the smooth operation of clinical trials. Responsibilities Oversee the day-to-day activities of clinical trials in accordance with GCP. Train and supervise research staff on proper procedures for conducting clinical trials per GCP. Prepare and submit all materials to the Institutional Review Board (IRB) and other regulatory bodies as required by the protocol. Maintain accurate subject logs, track expenses, and submit appropriate documentation to the Grant Administrator...

Position: Clinical Research Coordinator II, Clinical Research Network Location: Boston, MA Schedule: 40 hours per week ABOUT BMC: At Boston Medical Center (BMC), our diverse staff works together for one goal — to provide exceptional and equitable care to improve the health of the people of Boston. Our bold vision to transform health care is powered by our respect for our patients and our commitment to ensure everyone who comes through our doors has a positive experience. You’ll find a supportive work environment at BMC, with rich opportunities throughout your career for training, development, and growth and where you’ll have the tools you need to take charge of your own practice environment. POSITION SUMMARY: The Clinical Research Coordinator II (CRC II) procures, processes and ships research specimens and conducts patient recruitment, administers questionnaires, abstracts medical records, maintains patient databases, enters data into...

APPLY ASAP 4-6 Months Contract - Full-Time - On-Site Multiple locations available, please see other job postings. Barrington James is looking for a Clinical Research Coordinators to join our client who is ideally wanting individuals to start as soon as possible. This is a 4-6 month contract opportunity, this is a great opportunity to build a professional relationship with the client and to grow into other positions within the Clinical Research world. Brand new start up who have already won projects continuing to do so. Novel technology that will help change clinical trials for the better! Ability to train research naive sites and give insight where possible. Support patient recruitment and enrollment. Desired Experience: 2+ years of experience as a CRC (Minimum 2 year). Women's Health experience (Must). Oncology experience (desirable. Patient facing experience. Patient recruitment experience (MUST HAVE) Sample...

CANCER CENTER (IN-CANC-IUINA) The mission of the IU Simon Comprehensive Cancer Center (IUSCCC) Clinical Trials Office (CTO) is to support and facilitate the conduct of quality clinical research by IUSCCC translational clinical investigators. The CTO is a centralized resource available to all clinical investigators of the IUSCCC whose services enable the safe and efficient conduct of adult and pediatric trials. The CTO provides a comprehensive range of services. These services begin in the early stages of protocol development and continue throughout the study implementation, publication and long-term follow-up. Initiates and conducts protocol review, evaluations, study design, and risk assessments of clinical research studies. Participates in study budget negotiations and reconciles study budget accounts. Develops informational materials for recruitment of subjects; monitors enrollment goals and modifies recruitment strategy as needed. Oversees and ensures compliance...

Department CANCER CENTER (IN-CANC-IUINA) Department Information The mission of the IU Simon Comprehensive Cancer Center (IUSCCC) Clinical Trials Office (CTO) is to support and facilitate the conduct of quality clinical research by IUSCCC translational clinical investigators. The CTO is a centralized resource available to all clinical investigators of the IUSCCC whose services enable the safe and efficient conduct of adult and pediatric trials. The CTO provides a comprehensive range of services. These services begin in the early stages of protocol development and continue throughout the study implementation, publication and long-term follow-up. Job Summary Initiates and conducts protocol review, evaluations, study design, and risk assessments of clinical research studies. Participates in study budget negotiations and reconciles study budget accounts. Develops informational materials for recruitment of subjects; monitors...

Scheduled Hours 40 Position Summary Position assists investigators as coordinator of a basic to moderately complex clinical research study; may be responsible for multiple research studies simultaneously, responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance. Evening and weekend call is required for this position. Job Description Primary Duties & Responsibilities: Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends...