3614 research coordinator jobs found

Company : Allegheny Health Network Job Description : GENERAL OVERVIEW: This job plans, coordinates, and manages the activities associated with the initiation and completion of clinical trials, sponsored by internal, industry, foundation, and/or Federal funding sources. Maintains compliance with all regulatory bodies associated with human subject research. ESSENTIAL RESPONSIBILITIES: Interfaces with clinical staff to identify patients eligible for clinical trials. Provides in-service education to the appropriate hospital personnel in the departments involved with the investigational study. (30%) Interfaces with patients and their families to provide education regarding investigational studies, and requirements of participation to assure that they are informed prior to obtaining written consent. Completes required follow-up and active patient monitoring per study protocol. (30%) Collects, maintains, and stores all relevant clinical data, case report...

Job Title: Part time - Clinical Research Coordinator Job Description We are seeking an experienced Clinical Research Coordinator to assist a research site with an ophthalmology study in Chesterfield, MO. This is a contract position lasting approximately four months, with a commitment of 16 hours per week. This position requires previous clinical research experience and is not accepting relocation candidates at this time. Responsibilities Chart review and phone screening of potential patients Collect and enter data accurately and efficiently Resolve queries related to the research study Verify data to ensure accuracy and completeness Essential Skills Experience in clinical research, particularly in ophthalmology Previous experience as a Clinical Research Coordinator, ideally 2+ years Additional Skills & Qualifications Experience with ophthalmology clinical trials Work Environment The role operates within...

Job Summary: The University of Wisconsin Clinical Trials Institute (UW CTI) is a partnership between the University of Wisconsin School of Medicine and Public Health (SMPH) and UW Health. It supports clinical research professionals, investigators, and participants to advance discovery and research in the prevention, detection, and treatment of disease to help improve the health of individuals, families, and communities across Wisconsin and beyond. Our exceptionally talented workforce provides care, support, and information to clinical trials participants; resources, training, and guidance to research professionals; and opportunities for industry partners to advance groundbreaking medical research. The Clinical Research Coordinator Supervisor will supervise the UW CTI clinical research coordinators. They will have the responsibility of recruiting and hiring of new clinical research coordinator staff, take the lead in competency-based onboarding of new coordinators,...

Company Allegheny Health Network Job Description GENERAL OVERVIEW This job plans, coordinates, and manages the activities associated with the initiation and completion of clinical trials, sponsored by internal, industry, foundation, and/or Federal funding sources. Maintains compliance with all regulatory bodies associated with human subject research. Essential Responsibilities Interfaces with clinical staff to identify patients eligible for clinical trials. Provides in-service education to the appropriate hospital personnel in the departments involved with the investigational study. (30%) Interfaces with patients and their families to provide education regarding investigational studies, and requirements of participation to assure that they are informed prior to obtaining written consent. Completes required follow-up and active patient monitoring per study protocol. (30%) Collects, maintains, and stores all relevant clinical data, case report forms, and...

Job Summary: The University of Wisconsin Clinical Trials Institute (UW CTI) is a partnership between the University of Wisconsin School of Medicine and Public Health (SMPH) and UW Health. It supports clinical research professionals, investigators, and participants to advance discovery and research in the prevention, detection, and treatment of disease to help improve the health of individuals, families, and communities across Wisconsin and beyond. Our exceptionally talented workforce provides care, support, and information to clinical trials participants; resources, training, and guidance to research professionals; and opportunities for industry partners to advance groundbreaking medical research. The Clinical Research Coordinator Supervisor will supervise the UW CTI clinical research coordinators. They will have the responsibility of recruiting and hiring of new clinical research coordinator staff, take the lead in competency-based onboarding of new coordinators, performance...

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Part-Time Clinical Research Coordinator (Contract Position) Contract Duration: Open-ended contract (average duration is between 3-6 months) Job Type: Part-time 16 hours per week (Monday-Friday) - during normal business hours Start Date: ASAP Job Description We are seeking a part-time, onsite Clinical Research Coordinator (CRC) with experience in clinical research to support an ongoing Cardiovascular clinical trial. The ideal candidate will be able to work independently and act as one of the main CRCs for this study. Key Responsibilities Data Management: Collect study data and enter it into electronic data capture (EDC) systems. Query Resolution: Address and resolve data queries promptly. Qualifications Minimum of two years of experience as a Clinical Research Coordinator Specific experience with iMedidata and Inform electronic data capture (EDC) systems required Pay And Benefits The pay range for this position is $25.00 - $30.00/hr....

Department: Location: Health Sciences Center Time Type: Full time Worker Type: Regular Job Req ID: R104965 Minimum Requirements: Bachelor's degree in a related field or an equivalent combination of education and experience. Position Description: Under the direction of the Brown Cancer Center Clinical Trial Office leadership and in collaboration with a Research Nurse or Clinical Research Coordinator, the Clinical Research Coordinator IV assists in the coordination of daily activities related to the conduct of oncology clinical trials. The Clinical Research Coordinator IV assists with screening of potential patients, preparation and maintenance of research records, data collection, specimen processing and scheduling of research procedures. The Clinical Research Coordinator IV interacts with study participants in person or by telephone for follow up visits and simple assessment. Principal duties involve obtaining...

Department: Location: Health Sciences Center Time Type: Full time Worker Type: Regular Job Req ID: R104965 Minimum Requirements: Bachelor's degree in a related field or an equivalent combination of education and experience. Position Description: Under the direction of the Brown Cancer Center Clinical Trial Office leadership and in collaboration with a Research Nurse or Clinical Research Coordinator, the Clinical Research Coordinator IV assists in the coordination of daily activities related to the conduct of oncology clinical trials. The Clinical Research Coordinator IV assists with screening of potential patients, preparation and maintenance of research records, data collection, specimen processing and scheduling of research procedures. The Clinical Research Coordinator IV interacts with study participants in person or by telephone for follow up visits and simple assessment. Principal duties involve obtaining information for completing case report forms,...

Job Title: Clinical Research CoordinatorJob Description The Research Coordinator will assist an Investigator, Research Associate, or Project Manager with operationalizing the tasks associated with implementing a research study. This includes a variety of tasks related to recruitment, data collection, data management, and reporting of results. Responsibilities Recruits and consents research participants. Conducts telephone or in-person interviews with participants, including screening for eligibility. Performs follow-up by telephone, e-mail, and/or mail with study participants. Prepares, mails, and processes questionnaires and other study correspondence. Assists in tracking study participants using MS Excel. Keeps accurate and detailed records and files of work. Reviews, edits, cleans, and enters participant data into a database. May assist with literature reviews for proposal submissions and manuscript preparation. Handles...

Required Qualifications (Must be documented on all application materials) Bachelor’s Degree with 2 years of experience or a combination of education and work experience to equal 6 years Proficient computer experience to include Microsoft Word and Excel or similar software Demonstrated strong problem-solving skills, strong patient relation skills, and ability to work independently Willingness to assist in collection of body fluids (stool, urine, throat cultures, skin cultures), as required by study protocols. This does not include blood drawing, but blood samples will be handled. Able to provide proof of non-active tuberculosis and immunization for or resistance to measles, mumps, rubella, Hepatitis B, pertussis and influenza Preferred Qualifications: Bachelor’s Degree in biological or health care-related field. Previous experience working with patient databases and electronic medical records Previous clinical research experience, including data collection from study...

University of Colorado Anschutz Medical Campus Department: SOM Orthopedics Job Title: Clinical Research Coordinator, Open Rank Position #00808929 – Requisition 36792 Job Summary: The Dragoo Research Program, located at the Inverness Orthopedics and Spine Center - Steadman Hawkins Clinic, is seeking a Clinical Research Coordinator (CRC). The Clinical Research Coordinator (CRC) will engage in a variety of clinical research activities, including patient-oriented research, human subject studies, and laboratory procedures. Additionally, the CRC will be responsible for conducting standard complete blood count procedures for orthobiologic cases in a CLIA-accredited laboratory. Patient-oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new technologies. CRC professionals may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research. The CRC role requires...

Job Title: Clinical Research Coordinator Job Description The Research Coordinator will assist an Investigator, Research Associate, or Project Manager in operationalizing tasks associated with implementing a research study. This includes a variety of tasks related to recruitment, data collection, data management, and reporting of results. Responsibilities Recruit and consent research participants. Conduct telephone or in-person interviews with participants, including screening for eligibility. Perform follow-up with study participants via telephone, email, and/or mail. Prepare, mail, and process questionnaires and other study correspondence. Assist in tracking study participants using MS Excel. Maintain accurate and detailed records and files of work. Review, edit, clean, and enter participant data into a database. Assist with literature reviews for proposal submissions and manuscript preparation. Manage bookkeeping related to study budgets, including...

Job Title: Clinical Research Coordinator Job Description The Research Coordinator will assist an Investigator, Research Associate, or Project Manager in operationalizing tasks associated with implementing a research study. This includes a variety of tasks related to recruitment, data collection, data management, and reporting of results. Responsibilities Recruit and consent research participants. Conduct telephone or in-person interviews with participants, including screening for eligibility. Perform follow-up with study participants via telephone, email, and/or mail. Prepare, mail, and process questionnaires and other study correspondence. Assist in tracking study participants using MS Excel. Maintain accurate and detailed records and files of work. Review, edit, clean, and enter participant data into a database. Assist with literature reviews for proposal submissions and manuscript preparation. Manage bookkeeping related to study budgets, including...

Scheduled Hours 40 Position Summary Do not miss this opportunity to join WashU's Department of Surgery Urology Clinical Research Team. Urology Clinical Research Group is a small team of clinical research coordinators all reporting to the same manager. Although each coordinator has specific projects for which s/he is responsible, in many cases, projects require a team approach with coordinators relying heavily on each other for help and collaboration. Employee will work mainly with patients experiencing Urologic conditions/problems as well as, to a smaller degree, healthy volunteers. Specific patient population will depend on a project and will vary from one project to another. Typical day in Urology research is difficult to define as tasks will vary from day to day but common tasks in this position include, but are not limited to, medical records review, participant recruitment (by phone and/or in person) and consent. Employee will also be expected to conduct study visits, document...

Scheduled Hours 40 Position Summary Join our dynamic team, dedicated to advancing the field of pediatric cardiology through cutting-edge research. Our diverse portfolio of projects includes drug and device trials, comprehensive registries, and pioneering principal investigator-initiated studies. We are committed to improving the lives of children with heart conditions by exploring innovative treatments and therapies in a collaborative and supportive environment. If you are passionate about making a difference and contributing to meaningful advancements in pediatric cardiology, we encourage you to apply and be a part of our mission. This role assists investigators as coordinator of a basic to moderately complex clinical research study; may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; responsible for managing and recording all phases of study protocol as required...

Scheduled Hours 40 Position Summary Assists investigators as coordinator of a basic to moderately complex clinical research study; may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; responsible for managing and recording all phases of study protocol as required by the sponsoring agency to ensure compliance. 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...

Scheduled Hours 40 Position Summary Position assists investigators as coordinator of a complex clinical research study; may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance. Job Description Primary Duties & Responsibilities: Confers with PI to assist in developing plans for research projects and discuss the interpretation of results; collaborates in the preparation of manuscripts for publications and preparation of grant proposals to sponsoring agencies; assists in the preparation of amendments to protocols and/or modifications to study design as appropriate . Coordinates the development of forms, questionnaires, and the application of research techniques; assists in writing instructional procedure manuals for study progress,...

Scheduled Hours 40 Position Summary This position assists investigators as coordinator of a basic to moderately complex clinical research study; may be responsible for multiple research studies simultaneously, acting as a liaison with the school, sponsoring agency, community and the study participants; responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance. 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...

Scheduled Hours 40 Position Summary Position assists investigators as a data coordinator of clinical research trials of all complexities, extracting data from the Electronic Medical Record (EMR) and other source documents and entering it into an Electronic Data Capture (EDC).May be responsible for numerous research trials simultaneously. Helps ensure the accurate collection of study- required procedures while patients are receiving protocol treatment and are in active protocol follow-up; acts as liaison between the School, trial sponsors, vendors, and the study team. Responsible for helping the clinic coordinator and Principal Investigator (PI) manage and record data for all phases of study protocol as required by sponsoring agency to ensure compliance, patient safety and welfare, and data integrity. Job Description Primary Duties & Responsibilities: Assists in developing plans for research projects and discusses the interpretation of results;...

Careers With Purpose Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the United States. We're proud to offer many development and advancement opportunities to our nearly 50,000 members of the Sanford Family who are dedicated to the work of health and healing across our broad footprint. Facility: Sanford Broadway Med Cntr Location: Fargo, ND Address: 801 Broadway N, Fargo, ND 58102, USA Shift: 8 Hours - Day Shifts Job Schedule: Full time Weekly Hours: 40.00 Salary Range: $27.50 - $44.00 Department Details Monday-Friday schedule 8:00AM-4:30PM No night, weekends, or holidays Job Summary Provides an opportunity to learn daily and contribute to treatments of the future. Enthusiasm for learning required, along with participation in educating patients, physicians, nurses and other personnel to the research process. Advanced nursing position that involves clinical patient contact, research study...

Job Profile Summar y This role focuses on performing work related to research and development of new products, innovation, and improvement of products and processes. In addition, this role focuses on performing the following Research Programs and Projects duties: Supports the development of new products and innovation. Includes Clinical roles focused on research projects. Positions in this family perform basic, translational, and/or clinical research towards solving a specific problem for an entity or community. A professional individual contributor role that may direct the work of other lower level professionals or manage processes and programs. The majority of time is spent overseeing the design, implementation or delivery of processes, programs and policies using specialized knowledge and skills typically acquired through advanced education. An entry level role that applies broad theoretical job knowledge typically obtained through advanced education. May require the...

Scheduled Hours 40 Position Summary This position will be housed in the Radiology Clinical Research Core (RadCore) working directly with the Center for Clinical Theranostics Research (CCTR) coordinating clinical trials. Mallinckrodt Institute of Radiology’s clinical theranostics program provides personalized medical management through targeted radiopharmaceutical diagnosis and therapy. The theranostics program, which has been recognized as a Radiopharmarceutical Therapy Center of Excellence, is a collaboration between the Division of Nuclear Medicine and the Department of Radiation Oncology. Job Description Primary Duties & Responsibilities: Assists in developing plans for research projects and discusses the interpretation of results; collaborates in the preparation of manuscripts for publications and preparation of grant proposals to sponsoring agencies; assists in the preparation of amendments to protocols and/or modifications to study...

Thanks for your interest in Children's Mercy! Do you envision finding a meaningful role with an inclusive and compassionate team? At Children's Mercy, we believe in making a difference in the lives of all children and shining a light of hope to the patients and families we serve. Our employees make the difference, which is why we have been recognized by U.S. News & World Report as a top pediatric hospital, for eleven consecutive years. Children's Mercy is in the heart of Kansas City - a metro abounding in cultural experiences, vibrant communities and thriving businesses. This is where our patients and families live, work and play. This is a community that has embraced our hospital and we strive to say thanks by giving back. As a leader in children's health, we engage in meaningful programs and partnerships throughout the region so that we can improve the lives of children beyond the walls of our hospital. Overview The Research Data Coordinator I will perform a variety...