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Description Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. This role is responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB. This position is directly responsible to ensure that all documentation is timely and accurate and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH). Providence caregivers are not simp…
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Position Details
Description Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. This role is responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB. This position is directly responsible to ensure that all documentation is timely and accurate and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH). Providence caregivers are not simp…
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Position Details
Description Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. This role is responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB. This position is directly responsible to ensure that all documentation is timely and accurate and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH). Providence caregivers are not simp…
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Position Details
Description Independently coordinates research and administrative tasks in support of one or more research studies. Works with study investigators and supervisor to address study-related issues. Backs up other coordinators as needed. Supports department financial performance through budgeting, billing and as directed. Providence caregivers are not simply valued – they’re invaluable. Join our team at Swedish Research and thrive in our culture of patient-focused, whole-person care built on unders…
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Associate Clinical Research Coordinator at Providence Health and Services summary: The Associate Clinical Research Coordinator independently manages research and administrative tasks for multiple studies, collaborating with investigators and supporting department financials. This role requires knowledge of FDA regulations, medical terminology, and research protocols, with strong communication and organizational skills. Candidates should possess a relevant bachelor's degree or equivalent experie…
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Description Independently coordinates research and administrative tasks in support of one or more research studies. Works with study investigators and supervisor to address study-related issues. Backs up other coordinators as needed. Supports department financial performance through budgeting, billing and as directed. Providence caregivers are not simply valued – they’re invaluable. Join our team at Swedish Research and thrive in our culture of patient-focused, whole-person care built on unders…
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Position Details
Description Independently coordinates research and administrative tasks in support of one or more research studies. Works with study investigators and supervisor to address study-related issues. Backs up other coordinators as needed. Supports department financial performance through budgeting, billing and as directed. Providence caregivers are not simply valued – they’re invaluable. Join our team at Swedish Research and thrive in our culture of patient-focused, whole-person care built on unders…
Apply Now
Position Details
Description Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. This role is responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB. This position is directly responsible to ensure that all documentation is timely and accurate and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH). Providence caregivers are not simp…
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Position Details
Clinical Research Coordinator - Research Projects at Providence Health and Services summary: The Clinical Research Coordinator manages daily operations of multiple clinical research studies, ensuring compliance with study protocols and regulatory requirements. This role involves coordinating with investigators, patients, sponsors, and institutional review boards to maintain accurate and timely documentation. The position requires a background in medical or phlebotomy training, with experience i…
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Clinical Research Coordinator - Research Projects at Providence Health and Services summary: The Clinical Research Coordinator manages day-to-day operations of multiple clinical studies, ensuring compliance with protocols and timely documentation. They collaborate closely with Principal Investigators, patients, sponsors, and institutional review boards to maintain research integrity. This role requires relevant educational background and experience in clinical research settings, supporting pati…
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Position Details
Description Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. This role is responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB. This position is directly responsible to ensure that all documentation is timely and accurate and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH). Providence caregivers are not simp…
Apply Now
Position Details
Description Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. This role is responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB. This position is directly responsible to ensure that all documentation is timely and accurate and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH). Providence caregivers are not simp…
Apply Now
Position Details
It’s More Than a Career, It’s a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives…
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Job Description Job Description Job Title: Clinical Research Coordinator Job Description We are seeking an experienced Clinical Research Coordinator to join a dynamic team at one of the most prestigious academic research institutes in the world. You will be working with state-of-the-art equipment on high-profile studies sponsored by well-known organizations. Your role will be crucial in pioneering scientific discoveries in cancer research and translating these discoveries into new models of can…
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Job Description Job Description Job Title: Clinical Research Coordinator Job Description We are seeking a dedicated Clinical Research Coordinator to serve as the primary contact with research participants, sponsors, and regulatory agencies. You will coordinate clinical studies from startup through close-out, ensuring compliance with all protocols and regulatory requirements. This role offers the opportunity to work with one of the most renowned academic institutions in the US, providing a uniqu…
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Position Details
Job Description Job Description Looking for a strong Clinical Research Coordinator to join our team! This is a permanent role! Must have: 1 year of indsutry experience as a Clinical Research Coordinator Be okay with going on-site 100% Full-time Monday - Friday 8am - 5pm Responsibilities Supporting 6-8 studies at a time Sees patients 3-4 days per week, 5-10 patients per day Experience with prescreening, going through exclusion and inclusion criteria, consenting (20-30 pages) Experience submittin…
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Job Description Job Description Job Title: Clinical Research Coordinator Location: Chicago, IL (Irving Park Area) - 60641 Job Overview: Medix is currently seeking experienced Research Professionals wanting to grow their career in the Clinical Research Field. If you are interested in an opportunity to utilize your knowledge and skill set in the field as well as continue to learn research, apply below! Responsibilities/ Job Duties: Coordinates all aspects of the study including recruitment, conse…
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Position Details
Its More Than a Career, Its a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives o…
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Position Details
Job Title: Clinical Research Coordinator We are seeking a Clinical Research Coordinator to join our top-ranked research team. In this role, you will work under the general direction of the Principal Investigator to ensure all protocols are conducted in accordance with Good Clinical Practice (GCP) principles. You will play a critical role in coordinating clinical research studies, ensuring compliance with regulations, and maintaining high ethical standards. Key Responsibilities Develop strong w…
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