Clinical Research Coordinator
$27.93 - $35 per hourCenExel Rocky Mountain Clinical Research
CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k. Compensation : $27.93-$35.00/hour (Depending on education, experience, and skillset) Job Summary: Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies. Essential Responsibilities and Duties: Assists with coordinating all aspects of patient involvement from study initiation until study completion. Organizes research information for clinical trials. Observes subjects and assists with data analysis and reporting. Schedules the collection of data. Documents adverse events, protocol deviations, and other unanticipated problems appropriately. Reports research data to maintain quality and compliance. Performs administrative and regulatory duties related to the study as appropriate. Participates in other protocol development activities. Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.) Educates potential participants and caregivers on protocol specific details and expectations. Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned). Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive. Education/Experience/Skills: High school graduate or equivalent; Bachelors Degree, preferred. 0-3 years of experience in the medical field. Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials. Strong leadership and mentorship skills. Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level. Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations. Works independently as well as functioning as part of a team. Must be able to effectively communicate verbally and in writing. Working Conditions Indoor, Office environment. Shift work, depending on location. Essential physical requirements include sitting, typing, standing, and walking. Lightly active position, occasional lifting of up to 20 pounds. Rarely lift over 20 pounds. Reporting to work, as scheduled, is essential. Overnight travel may be required for training and/or investigative meetings. CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status. Qualifications Skills Behaviors : Motivations : Education Experience Licenses & Certifications Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor. #J-18808-Ljbffr
- ...Clinical Research CoordinatorThe Clinical Research Coordinator will be responsible for the oversight of research projects. In addition, the Clinical Research Coordinator must be able to provide efficient services to our physicians as well as provide quality, courteous...SuggestedWork at officeImmediate startAfternoon shift
- ...Job TitleResponsible for assisting with coordinating clinical trials with the strictest adherence to ICH, GCP, protocol, and company guidelines... ....Job DescriptionCenExel is a leading nationwide clinical research site and patient network serving the life sciences industry...SuggestedFull timeWork at officeShift workNight shift
- ...Clinical Research Coordinator IThe Clinical Research Coordinator I conducts and manages clinical trials in accordance with the study protocol, GCP, and Velocity's SOPs.ResponsibilitiesDuties/Responsibilities:Conduct and manage clinical trials in accordance with the study...SuggestedWork at officeFlexible hours
$60k - $75k
...Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Clinical Research Coordinator/RN in Littleton. Bring your established Oncology and or Research experience and join a team dedicated to providing...SuggestedTemporary workWork experience placementFlexible hours- ...informed consent process, and enrolls patients on protocol. Coordinates patient care in compliance with protocol requirements.... ...and education programs. Responsible for education of clinic staff regarding clinical research. May collaborate with Research Site Leader in the...Suggested
- Denver is seeking a Clinical Research Coordinator in Littleton, Colorado. The role involves overseeing clinical research projects and providing exceptional service to patients and physicians. Responsibilities include ensuring compliance with regulations, managing study...Work at office
- A clinical research organization is seeking a qualified candidate to coordinate patient care and manage trial protocols with responsibilities including data collection, patient screening, and maintaining compliance with regulatory standards. Candidates should have an associate...
$71.26k - $123.22k
...DOWNING ST City: DENVER State: Colorado Postal Code: 80210 : Executes and coordinates the informed consent process for participants in clinical trials and research studies. Screens potential research participants to determine eligibility for clinical...Full timeWork experience placementWork at officeLocal areaFlexible hoursShift work- ...Job Summary We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory...Full timeWork at officeMonday to FridayShift workWeekend work
- ...ECN Operating LLC is seeking a Lead Clinical Research Coordinator to oversee day-to-day study operations, ensure protocol compliance, and mentor the coordinator team. You will manage start-up through close-out, maintain data integrity, and coordinate with sponsors and...
- ...A leading healthcare organization is seeking a Clinical Research Coordinator (CRC) in Denver, Colorado. The CRC will manage clinical trials, recruit participants, and ensure compliance with regulatory guidelines. Ideal candidates have relevant degrees, strong organizational...Full time
$72.2k - $100k
...The Lead Site Clinical Research Coordinator (CRC) is the founding coordinator for Salma Health's Fremont clinic, responsible for establishing research operations at the site and managing day-to-day study conduct, including the ATLAS study and sponsored trials. The role...$23.31 - $34.97 per hour
...Location Aurora Position Type Regular Regular/Temporary Regular Add to Favorite Jobs Email this Job Job Overview Summary The Clinical Research Coordinator Associate is responsible for participating in the day-to-day operations of routine, minimally complex clinical research...Hourly payTemporary workImmediate startMonday to FridayShift workWeekend work$34 - $39 per hour
...Valkyrie Clinical Trials (VCT) , a Flourish Research Company, is a leading Oncology multi-site clinical research network with expertise in Oncology research... ...! We are actively hiring a Senior Clinical Research Coordinator to supportour Valkyrie Clinical Trials Denver,...Hourly payCasual workWork at officeImmediate startMonday to FridayFlexible hoursNight shiftDay shift$34 - $39 per hour
...Senior Clinical Research CoordinatorValkyrie Clinical Trials (VCT), a Flourish Research Company, is a leading oncology multi-site clinical... ...CELEBRATE YOU!We are actively hiring a Senior Clinical Research Coordinator to support our Valkyrie Clinical Trials Denver, Colorado...Hourly payMonday to FridayDay shift$32 - $39 per hour
...Senior Clinical Research Coordinator Role in Lakewood, CO (80228) Role Summary We are seeking an experienced Senior Clinical Research Coordinator (CRC) to lead oncology clinical trials. You will be responsible for end-to-end study management, ensuring strict adherence...Work at officeMonday to Friday- ...Position Summary The Lead Clinical Research Coordinator (Lead CRC) is responsible for managing and coordinating the day-to-day operations of clinical research studies, while also providing site-level leadership, mentorship, and oversight to the coordinator team. Reporting...Work at officeAfternoon shift
$26.99 - $40.48 per hour
...person to join our Children's Oncology Group Research Team here at Children's Hospital... ...disorders. We provide access to breakthrough clinical trials to the patients and families we... ...do it. Join us! The Clinical Research Coordinator Senior is a seasoned coordinator who can...Hourly payFull timeImmediate startMonday to FridayShift work- University of Colorado Anschutz Medical Campus in Aurora is seeking an Open Rank Clinical Research Coordinator (Entry - Senior) to oversee day-to-day operations of clinical trials and ensure compliance with Good Clinical Practice (GCP). The role requires a Bachelor's degree...
- The University of 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...
- Children's Colorado is seeking a Clinical Research Coordinator Associate to participate in day-to-day operations of routine clinical research programs at the University of Colorado Anschutz Medical Campus. The role involves data collection, documentation, and ensuring study...
- University of Colorado Anschutz Medical Campus is seeking a Clinical Research Coordinator (Breast Team) to support multiple clinical trials. The role involves daily trial operations, data abstraction, eligibility assessments, informed consent, and coordination with clinical...
$100k - $190k
...A leading clinical research organization is seeking a Clinical Trial Project Manager in Denver, CO. This role includes managing clinical trial operations, serving as the primary contact for sponsors, and ensuring compliance with ICH/GCP standards. Candidates should have...Flexible hours$78.64k - $90k
CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired...Full time$40.4 - $56.56 per hour
...history and tests ordered. Provide ongoing education initiatives and leads or contributes to special projects aimed at enhancing clinical operations within the department and across the organization. Manages scheduling and communication by utilizing decision trees...Temporary workPart timeLocal areaFlexible hoursShift work- Denverurology in Littleton, Colorado, is seeking a Clinical Research Coordinator to oversee research projects and provide quality service to both physicians and patients. Responsibilities include maintaining compliance with regulatory guidelines, working directly with patients...
- ...Clinical Trial Manager - Full Service Syneos Health is a leading fully integrated biopharmaceutical... ...Recruitment and Data Management to coordinate delivery handoffs and meet expected... ...to the successful conduct of a clinical research project. Demonstrates critical thinking...Contract workRemote workFlexible hours
- Syneos Health is seeking an Experienced Clinical Project Manager for an inflammation program, with sponsor-dedicated/remote US-only scope. The role emphasizes end-to-end trial execution, cross-functional leadership, and strong CRO/vendor oversight in a fast-paced environment...Remote job
$100k - $190k
Join to apply for the Clinical Trial Project Manager - Denver, CO role at Medpace Be among the first 25 applicants Job Summary Medpace... ...site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables Qualifications...Full timeContract workTemporary workWork at officeLocal areaImmediate startWork from homeFlexible hours$70k - $90k
A leading clinical research organization in Denver is seeking an Associate Clinical Trial Manager with a PhD and cardiology experience. This full-time office-based role involves managing project activities, ensuring accuracy in tasks, and maintaining project status reports...Full timeWork at officeFlexible hours
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