Clinical Research Associate: Regulatory & Study Coordination
Denver Research Institute
Denver Research Institute in Denver, CO is seeking a Professional Research Associate to support day-to-day operations and study coordination for research, evaluation and implementation projects within the Denver Veteran’s Health Administration. Under supervision of the Principal Investigator and/or Program Manager, you will recruit participants, manage data, liaise with regulatory bodies, prepare regulatory packages, and maintain study records across lifecycles. #J-18808-Ljbffr Denver Research Institute
- Children's Hospital Colorado is seeking a Clinical Research Coordinator Associate in Aurora, CO. The role supports... ...visits, data collection, regulatory tasks and participant interactions... ...candidates have a Bachelor of General Studies and may have related equivalency. Oncology...Regulatory
$23.32 - $34.97 per hour
...Regular/Temporary: Regular Summary The Clinical Research Coordinator Associate is responsible for participating in... ...clinical research programs and/or studies conducted by Principal... ...throughout the startup process. Assists regulatory team with Institutional Review Board...RegulatoryHourly payTemporary workImmediate startShift work$74.5k - $197.5k
...that sites are conducting the study(ies) and reporting study... ...contracted scope of work and Good Clinical Practice. Work with sites... ...studies by tracking regulatory submissions and approvals, recruitment... ...experience as a Clinical Research Associate (CRA) in a CRO, sponsor, or...RegulatoryFull timePart timeLocal areaImmediate startWorldwide- ...Medical Campus's Cancer Center is seeking an entry-level Regulatory Compliance Coordinator to support FDA/GCP compliant trials, including NCTN and ETCTN... ...OnCore and eReg, and assist with investigator onboarding while supporting study oversight. #J-18808-Ljbffr CU DenverRegulatory
$125k - $140k
...skills, knowledge, and clinical judgement to provide a... ...based upon clinical research standards. Responsibilities... ...for all aspects of study site monitoring... ...according to the applicable regulatory requirements Ensure... ...eg. co-monitoring Coordinate designated clinical...RegulatoryWork at officeLocal areaNight shift$125k - $142k
...skills, knowledge, and clinical judgement to provide a... ...based upon clinical research standards. Responsibilities... ...for all aspects of study site monitoring... ...according to the applicable regulatory requirements Ensure... ...eg. co-monitoring Coordinate designated clinical...RegulatoryWork at officeLocal areaNight shift$52.86k - $67.24k
...Cancer Center - Cancer Clinical Trails Office (Regulatory Team) Working Title... ...Regulatory Affairs Coordinator (Open Rank)... ...and submitting all study-related regulatory... ...of record, UCHealth Research Administration); and... ...Clinical Research Associate Conditions of Employment...RegulatoryWork experience placementWork at office3 days per week$71.52k - $90.97k
...Department: Medicine - Division of Cardiology Job Title: Regulatory and Compliance Coordinator Position #: 00804856 - Requisition #: 41659 Job... ...regulatory resource for a diverse portfolio of clinical research studies. This position supports investigators and research...RegulatoryLocal area3 days per week$52.86k - $67.24k
...Department: Cancer Center (Cancer Clinical Trials Office - Regulatory Team) Working Title: Regulatory Compliance Coordinator (Entry Level) Position #: 0... ...complexity or lower-acuity studies, including studies in long-... .... Assures adherence to research standards established by...RegulatoryWork at officeLocal area3 days per week- ...CO, seeks a Neuropsychiatry Clinical Research Professional to support neuromodulation... ...research and translational studies within the Psychiatry... ...research protocols, coordinate human-subjects research activities, and assist with regulatory documentation, grants, and manuscripts...Regulatory
- ...Job TitleResponsible for providing Clinical Research support for all clinical trials.Job DescriptionUnder... ...will serve as support for the clinical study team. Essential Duties And... ...for procurement of budgets, contracts, regulatory documents, and other administrative documents...Regulatory
- ...Medical Campus is seeking an Open Rank Research Services Clinical Research Coordinator (Entry - Intermediate) to... ...coordination of clinical trials, regulatory compliance, data management, and... ...Aurora, CO. The position supports studies on esophageal diseases, including...Regulatory
- ...Department of Surgical Oncology seeks a Clinical Research Coordinator V to oversee enrollment, accrual and... ..., sponsors, monitors and regulatory bodies to ensure safety and efficient... ...accurate data management, and timely study completion, with compensation commensurate...Regulatory
- ...Parexel is a leading global clinical development partner... ...biopharmaceutical companies and research sites to design and... ...seeking a Clinical Research Associate (CRA) with a minimum of... ...teams and helping ensure study quality, patient safety, regulatory compliance, and accurate...RegulatoryWork at officeRemote workWorldwideFlexible hours
- The University of Colorado Anschutz Medical Campus is seeking a Regulatory Affairs Coordinator to support the Cancer Clinical Trials Office. You will manage regulatory submissions, draft consent documents, and coordinate reviews across multiple boards for Phase I-IV trials...RegulatoryWork at office
- Clinical Research Associate - Full-Service Syneos Health is a fully integrated biopharmaceutical solutions... ...on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiology... ...effective conduct of clinical study data review and capture, and verify site...RegulatoryInterim roleLocal areaImmediate startRemote workFlexible hours
- KeHE Distributors is seeking a Food Safety Coordinator to uphold safety, quality, and regulatory compliance across our distribution centers. You will conduct inspections, monitor controls, and ensure GMP/GDP adherence while aligning with KeHE’s mission and values. The role...Regulatory
- ...commercialization, offering expertise in regulatory strategy, clinical trial design and execution, market... ...ensure that sites are conducting the study(ies) and reporting study data as... ...skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical...RegulatoryLocal area
$110.52k - $138.15k
...global healthcare intelligence and clinical research organisation united by a mission to... ...trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice... ...experience as a Clinical Research Associate, with a strong understanding of...Regulatory- ...more years of relevant research experience, or an... ...the direction of the clinical Principal Investigators... ...the Clinical Research Coordinator V is responsible for the... ...multiple clinical research studies. The Clinical Research... ..., monitors and regulatory entities to ensure the...RegulatoryFull timeContract workWork experience placementWork at office
- ...currently looking for a Clinical Research Associate to join us. This position... ...subjects involved in a clinical study are protected.... ...the Study Start-up Group to coordinate activities with the site in... ...initiation of studies. Obtains regulatory documentation for...RegulatoryPermanent employmentWork from home
$45.31 - $67.01 per hour
...Description: The RN Program Coordinator is a hospital or care site level... ...who provides specialized clinical expertise, consultation, education, and research within their designated area or... ...with state, national, and other regulatory agency requirements for disease...RegulatoryHourly payRemote workShift work$85k - $93k
...testing and in agroscience Contract Research Organisation services. Eurofins is... ...sciences and in the support of clinical studies, as well as having an emerging global... ...General Job Description The Regulatory Affairs (RA) Coordinator is responsible for ensuring the...RegulatoryFull timeContract workWork at officeLocal area- ...Job Title: Clinical Research Coordinator (Registered Nurse / RN) Location: Denver, CO (100% In-Person... ...care with vital administrative and regulatory duties. Who We Are Looking For... ...Administrative / 40% Patient-Facing Active Studies: ~90 total active trials at the...RegulatoryFull time
$56.39k - $104.87k
...compliance with organizational standards and regulatory requirements. Negotiates contract terms... ...and stakeholders. Collaborates with clinical and support staff to optimize reimbursement... ...:Bachelor's [Preferred]Field of Study: from a four-years college or universityWork...RegulatoryContract work$48.45k - $61.62k
...Job Title: Tissue Bank Coordinator (Open Rank, Entry to... ...Bank Coordinator is a Clinical Science Professionalposition... ...performs clinical research related functions... ...epidemiologic and behavioral studies and/oroutcomes... ...Monitoring Committee (DSMC), Regulatory AffairsCoordinator....RegulatoryLocal area- ...Description The role independently coordinates programs and special projects,... ...programs, pilots, and organizational studies (e.g., GPS Program, Climate Studies,... ...access to facilities documents; Research and draft new regulatory or facility policies when gaps arise...RegulatoryPermanent employmentWork at officeNight shift
- ...Campus in Aurora, CO is seeking an Open Rank Data Coordinator (Entry - Senior) to oversee day-to-day clinical trial operations and data management within the... ...informed consent, subject interviews, data capture, and regulatory compliance, with salary ranges aligned to entry...Regulatory
- ...Colorado Anschutz Medical Campus is seeking a Tissue Bank Coordinator to perform clinical research activities across entry to senior levels. This role involves screening, consent, data capture, and regulatory compliance in a hospital-based setting. The position is onsite...Regulatory
- ...University of Colorado Anschutz Medical Campus Division of Cardiology seeks a Regulatory and Compliance Coordinator to serve as a principal regulatory resource for a diverse portfolio of clinical studies. This role supports investigators and teams through feasibility, start-...Regulatory
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