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$61.11k - $67.9k
The Regulatory Coordinator II (RC II) will work under the direction of the Director of Clinical Research Administration for the Clinical Trials Office to complete the regulatory requirements of the clinical research projects. The RC coordinates aspects of protocol submissions...SuggestedWork at officeLocal areaRemote work2 days per week3 days per week- University of Kansas Medical Center is seeking a Laboratory Coordinator for the Correlative Lab in the Cancer Center. The role involves coordinating collection and shipment of oncology trial specimens, managing supplies, and assisting with start-up activities. The position...Suggested
- The University of Kansas Health System is seeking a Senior Laboratory Coordinator to coordinate oncology clinical trial specimens and supplies per protocol, including pharmacokinetics and pharmacogenomics studies. You will support industry-sponsored and investigator-initiated...Suggested
- ERA Health Research, LLC in Redmond, WA, seeks a Full-Time Regulatory and Data Coordinator I to support clinical trial operations, regulatory documents, data quality, and monitoring visit prep. The role offers a hybrid work model with on-site training during the initial...SuggestedFull timeRelocation
- Pragmatic in West Orange, NJ is hiring a Clinical Research Coordinator (CRC) or Senior CRC to lead IDE and post-market medical device trials at the site, working directly with physicians in a fast-growing clinical research network. You’ll own studies day-to-day, coordinate...Suggested
- The Fred Hutchinson Cancer Center in Seattle seeks a Clinical Research Coordinator II to coordinate interventional Phase I-III clinical trials and observational studies across disease programs. You will manage participant screening, enrollment, visit coordination, data...Suggested
- Pacific American Fish Company (PAFCO) is seeking an R&D Coordinator in Vernon, CA to support product development, reformulation, and commercialization... ...our seafood manufacturing environment. You will coordinate trials, manage documentation, ensure regulatory compliance, and...Suggested
$31 - $41 per hour
Department Provost URA: Clinical Trials Contracting About the Department University Research Administration has the responsibility... ...transfer agreements and clinical trials. Job Summary The Agreement Coordinator - Clinical Trials sits within the Research Contracts Group at...SuggestedHourly payContract workWork experience placementWork at officeRemote workFlexible hoursAfternoon shift- ...Orange County and the world by providing life-saving clinical trials designed to strengthen and accelerate the pathway of discovery... ...accurate information and assist Principal Investigators and study coordinators with all regulatory aspects of non-cancer-related trials. The...SuggestedWork experience placementWork at officeLocal area
- ERA Health Research is seeking a Full-Time Regulatory and Data Coordinator I to support clinical trial operations from Redmond, WA. The hybrid role includes regulatory document management, ED C data entry, IRB submissions, and monitoring visit preparation as part of a cross...SuggestedFull time
- The University of Kansas Medical Center in Kansas City is seeking a Senior Laboratory Coordinator to oversee oncology trial specimens, including pharmacokinetics and pharmacogenomics, across Industry-Sponsored, Cooperative Group and Investigator Initiated studies. You will...Suggested
- The University of Kansas Medical Center Cancer Center is seeking a Regulatory Coordinator to manage study-specific regulatory and safety reporting across multiple trials. This role ensures compliance with CFR, GCP, HIPAA and KUMC policies, and serves as the primary contact...SuggestedRemote job
- ...'s Premium Quality Seasonings & Sauces is hiring for a sample coordination role based in Walnut Creek, California. You will coordinate ingredient... ..., and support product development and co-manufacturer trials to ensure timely availability of materials. This role emphasizes...Suggested
- Dana-Farber Cancer Institute in Brookline, MA seeks a Regulatory Coordinator II to manage regulatory requirements for clinical research projects under the Clinical Trials Office. You will prepare submissions, maintain study records, and ensure compliance with DFCI/DF/HCC...SuggestedWork at officeRemote work
- The University of Kansas Cancer Center is seeking a Senior Laboratory Coordinator (Correlative Lab) to coordinate oncology trial specimen collection, processing, and shipping for pharmacokinetics and pharmacogenomics studies across industry-sponsored and investigator-initiated...Suggested
- The University of Kansas Medical Center Cancer Center is seeking a Laboratory Coordinator (Correlative Lab) to coordinate the collection, processing, and shipping of oncology trial specimens in accordance with protocol requirements. This 100% onsite role supports the Clinical...Work at office
- Re:Cognition Health, a brain and mind clinic in Fairfax, VA, is seeking a Clinical Trials Coordinator to oversee activities across the full trial lifecycle, from startup to closeout, while collaborating with investigators, sponsors, and cross-functional teams. You will...Private practice
- HonorHealth Research Institute in Scottsdale is seeking a Coordinator I - Research Infusion Authorization to initiate and obtain prior authorizations for clinical-trial and continuing-care infusion and chemotherapy treatments. You will collaborate with pharmacists, clinicians...
- The University of Kansas Medical Center Cancer Center is seeking a Regulatory Coordinator to manage study-specific regulatory and safety reporting across multiple clinical trials. You will ensure compliance with CFR, GCP, HIPAA and organizational policies. Responsibilities...Remote job
- Pragmatic is hiring at the Wilmington, DE site for Clinical Research Coordinators (CRC) and Senior CRCs. You will partner with physicians to lead device trials, manage day-to-day study activities, and work within a growing network with occasional South Jersey travel. Responsibilities...
- ...is seeking an experienced Litigation Paralegal to support complex matters across the firm's litigation practice. The role emphasizes trial readiness, meticulous document management, and collaboration with attorneys, paralegals, and staff. Ideal candidates will have 4-12...
$75k - $100k
...Environmental Conditions Office Job Description The Home Trial Services Global Project Manager is responsible for overseeing... ...timelines for each assigned project. · Meets with internal teams to coordinate efforts, provide recommendations and risks and mitigation...Temporary workWork at officeLocal areaRemote work- COG Research Foundation, LLC, a California nonprofit, seeks a Regulatory Audit Coordinator to conduct regulatory audits for COG institutions, reviewing IRB submissions and ensuring compliance with COG policies and federal regulations. This role emphasizes meticulous regulatory...Remote job
- ...and the IRB, ensuring compliance with NU-, local-, state-, and federal regulations. The role involves preparing IRB submissions, coordinating renewals and modifications, and supporting data management and study documentation across various clinical research #J-18808-...Local area
- A prominent medical institution in Kansas City is seeking a Clinical Research Coordinator to manage clinical studies. This full-time role involves recruiting and educating patients, maintaining documentation, and ensuring regulatory compliance. Candidates should have a...Full time
- ...about Valeris, please visit As a Program Manager on the Clinical Trial Support (CTS) team, you will be the primary liaison between... ...the third-party service vendor landscape in order to manage and coordinate client vendor relationships (agencies, SPPs, HUBs, service providers...Full timeContract workTemporary workWork at officeImmediate start
- The University of Texas at Austin is hiring a Clinical Research Associate II in the Department of Neurology to support funded research studies. The role focuses on scheduling, patient interaction, study administration, and regulatory compliance, reporting to the Principal...
- ...redefining cancer care around the world. As the Regulatory Coordinator you are responsible for managing and planning regulatory... ...oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last...Local area
$50k
...about Valeris, please visit As a Program Manager on the Clinical Trial Support (CTS) team, you will be the primary liaison between... ...the third-party service vendor landscape in order to manage and coordinate client vendor relationships (agencies, SPPs, HUBs, service providers...Full timeContract workTemporary workWork at officeImmediate start- ...Country Approval Specialist manages the preparation, review and coordination of Country Submissions in line with global submission strategy... ..., in accordance with agreed timelines. • Ensure that trial status information relating to SIA activities are accurately maintained...Contract workWork at officeLocal area