Clinical Research Associate, Sponsor Dedicated
$71.9k - $189kIQVIA
Durham, North Carolina, United States of America
Aurora, Illinois, United States
San Fernando, California, United States
Clinton, Missouri, United States
Mansfield, Ohio, United States
Santa Cruz, California, United States
Santa Fe, New Mexico, United States
South Shore, Illinois, United States
Elk Grove, California, United States
Hudson, Ohio, United States
Englewood, Colorado, United States
Bellingham, Washington, United States
Marysville, Washington, United States
Overland Park, KS, United States of America
Evanston, Wyoming, United States
La Habra, California, United States
Prescott, Arizona, United States
Westchester, New York, United States
Mount Vernon, Illinois, United States
Warren, Ohio, United States of America
Linden, New Jersey, United States
Fremont, California, United States
Del Mar, California, United States
Lake Tahoe, California, United States
Northfield, New Jersey, United States
Fort Pierce, Florida, United States
Wilkes Barre, Pennsylvania, United States
Camden, New Jersey, United States
Lancaster, California, United States
Clarksville, Tennessee, United States
Adair, Iowa, United States
Fort Collins, Colorado, United States
Breckenridge, Colorado, United States
Littleton, Colorado, United States
Liverpool, New York, United States
Ft Lauderdale, Florida, United States
Springfield, Ohio, United States
Long Island, New York, United States
Gloucester, Virginia, United States
West Point, Virginia, United States
O'Fallon, Illinois, United States
Cheyenne, Wyoming, United States
Manhattan, New York, United States
New City, New York, United States
Parsippany, New Jersey, United States of America
Queens, New York, United States
New York City, New York, United States
Escondido, California, United States
Oak Brook, Illinois, United States
Merritt Island, Florida, United States
El Cajon, California, United States
Ontario, California, United States
Afton, Wyoming, United States
Abilene, Texas, United States
Orangevale, California, United States
Abingdon, Virginia, United States
Orland Park, Illinois, United States
Shenandoah, Texas, United States
Akron, Ohio, United States
Paradise Valley, Arizona, United States
Newark, Delaware, United States
Hollywood, Florida, United States
Port Saint Lucie, Florida, United States
Lawton, Oklahoma, United States
Portland, Oregon, United States
Chino Hills, California, United States
Belmar, New Jersey, United States
Sonora, California, United States
Berkley, California, United States
Springfield, Massachusetts, United States
Springfield, Missouri, United States
San Jose, California, United States
Beverly Hills, California, United States
Melbourne, Florida, United States
Colorado Springs, Colorado, United States
St. Petersburg, Florida, United States
Panama City, Florida, United States
Redondo Beach, California, United States
Crystal Lake, Illinois, United States
Rochester, New York, United States
Ada, Oklahoma, United States
Kansas City, Missouri, United States
Ainsworth, Nebraska, United States
Carlsbad, CA, United States of America
Denver , Colorado, United States
Full time
R1541733
To be eligible for this position, you must reside in the same country where the job is located.
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Essential Functions
• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
Qualifications
• Bachelor's Degree Degree in scientific discipline or health care preferred.
• Requires at least 2 years of year of on-site monitoring experience.
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Good therapeutic and protocol knowledge as provided in company training.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $71,900.00 - $189,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
$71.9k - $189k
...applicable regulations and guidelines, and sponsor requirements.Essential Functions•... ...with contracted scope of work and Good Clinical Practice.• Work with sites to adapt, drive... ...skill in applying, applicable clinical research regulatory requirements.• i.e., Good Clinical...SuggestedFull timePart timeLocal areaImmediate startWorldwide$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology Phase I - Denver, CO ICON plc is a world-leading healthcare... ...~ Experience supporting sites and/or sponsors in regulatory inspections ~... ...to our culture and values. We're dedicated to providing an inclusive and accessible...SuggestedWork experience placementInterim roleLocal areaRemote workFlexible hoursICON plc
Denver, CO2 days ago- ...Clinical Research Associate - Full-Service Syneos Health is a leading fully integrated biopharmaceutical... ...what unites us globally, and we are dedicated to taking care of our people. We are... ...attends Investigator Meetings and/or sponsor face to face meetings. Participates in...SuggestedContract workInterim roleLocal areaImmediate startRemote workFlexible hours
Syneos Health/ inVentiv Health Commercial LLC
Denver, CO3 hours ago $87.2k - $169.3k
...Senior CRA 1 IQVIA Early Clinical Development is hiring for a Senior CRA 1.... .... Job Overview We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key... ..., regulatory requirements, and sponsor expectations. Your work will directly...SuggestedFull timePart timeImmediate startWorldwideAvery Healthcare Group Ltd.
Denver, CO5 days ago$96.2k - $151.4k
...site manager throughout all phases of a clinical research study, taking overall responsibility of allocated... ...activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.Gains an in-depth understanding...SuggestedFull timeFor contractorsLocal areaRemote workFlexible hours2 days per week3 days per week- ...experience is strongly preferred. Job Purpose: The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies... ...) as directed by LSAD or line manager. Compliance with Sponsor Standards Ensures compliance with the Client's Code of...Local areaRemote workFlexible hoursShift work
PAREXEL
Denver, CO1 day ago - ...the fastest growing CROs. We are currently looking for a Clinical Research Associate to join us. This position is permanent, home-based, must... ...validation of source documentation as required by sponsor. Prepares monitoring reports and letters in a timely manner...Permanent employmentWork from home
Tigermed America
Denver, CO19 days ago - ...Identify and resolve site-level issues, escalating risks to the Clinical Team Lead/PM as appropriate Review and ensure completeness of... ...inspection readiness at site and study level Liaise directly with sponsors on site status, risk mitigation, and study progress as needed...Remote work
- ...with Waters. Waters is a global leader in life sciences, dedicated to accelerating the benefits of pioneering science through... ...dreams into possibilities. Summary Job Description The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical operations...Hourly payContract workRemote workWorldwideShift work
- Clinical Research Associate - Full-Service Syneos Health is a fully integrated biopharmaceutical solutions organization focused on accelerating... ...requirements. Prepare for and attend investigator meetings, sponsor face‑to‑face meetings, global clinical monitoring/project...Interim roleLocal areaImmediate startRemote workFlexible hours
- ...Company Description PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect... ...of therapeutic indications. Job Description As a Lead Clinical Research Associate, you will hold a leadership role within the study team, overseeing...Contract workRemote workWork visa
GrabJobs
Westminster, CO3 days ago - ...Clinical Research Associate Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee, this position will serve as support for the clinical study team. Essential Duties And Responsibilities Participate...
Allen Spolden
Denver, CO2 days ago $19 - $21 per hour
...Research Assistant ICenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase... ...entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract...Full timeContract workWork at officeCenExel
Englewood, CO1 day ago$19.5 - $26.48 per hour
...of this position is to assist in duties and activities associated with supporting clinical research and research studies at Intermountain Healthcare. A... ...compliance with Intermountain policy and procedure, research sponsors and federal rules and regulations. Collaboration &...Hourly payFull timeRemote workMonday to FridayIntermountain Health
Denver, CO3 days ago$19.33 - $27 per hour
Join the HJF Team! HJF is seeking a Clinical Research Assistant I to perform data collection by conducting research interviews. The Clinical... ...of Military Medicine (HJF) is a nonprofit organization dedicated to advancing military medicine. We serve military, medical,...Hourly pay16 hoursPart timeFor contractors$125k - $140k
...What You Will Do You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants... ...trials and respond to emergency situations based upon clinical research standards. Responsibilities: Responsible for all aspects...Work at officeLocal areaNight shift$56.55k - $71.94k
...Critical Care Job Title: OPEN RANK Research Services Professional (Senior... ...rebudgeting from OGC and/or sponsor when required Prepares... ...tremendous and sustained growth. The clinical practice sites have built new... ...Anschutz Medical Campus is dedicated to ensuring a safe and secure...Full timeContract workTraineeshipLocal area2 days per week3 days per week$56.55k - $71.94k
...Critical Care Medicine Job Title: Research and Grants Specialist (Open... ...projects, industry-sponsored projects, andmulti-investigator... ...tremendous and sustainedgrowth. The clinical practice sites have built new... ...Anschutz Medical Campus is dedicated toensuring a safe and secure...TraineeshipLocal area$25.9 - $34.57 per hour
...Research & Quality Lab TechnicianYour role:As the Research & Quality Lab Technician you will be responsible for supporting the Ardent... ...and Disability Programs • Voluntary Benefit Programs • Company Sponsored Wellness Programs • Retirement Savings with Company Match •...Work at officeFlexible hoursArdent Mills
Denver, CO4 days ago$20 - $27 per hour
...labelling is accurate. Eurofins is dedicated to delivering testing services that contribute... ...sciences and agroscience contract research services. It is one of the market leaders... ...material sciences and in the support of clinical studies, as well as having an emerging...Hourly payFull timeContract workMonday to FridayEurofins USA Environment Testing
Arvada, CO8 days ago$39.5 per hour
Openings as of 8/24/2026 Forensics/Debate Assistant Sponsor, Littleton High School JobID: 13953 Position Type: High School Athletics... ...competition events, facilitating acquisition of literacy material and research information for competitions Conducting practices and drills...Weekend workAfternoon shift- SUP - Assistant School Spirit Sponsor - Drill JobID: 7889 Date Posted: 2/20/2026 Location: Adams City High School Closing Date: 02/... ...reflects high standards and school pride. Requirements | Skills Associate’s Degree or higher (Bachelor’s Degree preferred) Three years...Temporary workSeasonal work
- ...IQVIA is a leading global provider of clinical research services, supporting trials across life sciences and healthcare. The role focuses on assisting in the conduct of clinical trial activities in compliance with regulations, emphasizing communication, prioritization,...
IQVIA Argentina
Lakewood, CO1 day ago - ...Denver Health Medical Center in Denver seeks a Senior Research Assistant to support clinical research and quality improvement initiatives. Under supervision, the RA assists with data collection, chart reviews, and regulatory compliance across multiple sites including...
Denver Health Medical Center
Denver, CO1 day ago - ...following functional areas: Research Operations Endpoint and... ...of professional experience (clinical research experience... ...Opportunity Employer CPC is dedicated to the principles of equal employment... ...traits historically associated with race, such as hair texture...Local areaImmediate startRemote workFlexible hoursShift work
CPC Clinical Research
Aurora, CO5 days ago - ...diagnostic outcomes that change lives. You'll become part of a dedicated team, supported by a holistic benefits package designed to... ...guidelines. Qualifications ~ Hold a Bachelor's degree in Clinical or Medical Laboratory Science, or possess an equivalent allied...Full timeLocal areaWeekend workDay shift
MLee Medical Employment
Denver, CO2 days ago $30.4k - $75.9k
...Clinical Trial Assistant This individual will play a key role in assisting in the conduct... ...and respect between the clinic and the research office Assists with the screening,... ...follow up care Comply with company and Sponsor policies, standard operating procedures...Full timePart timeWork at officeImmediate startWorldwideIQVIA Holdings
Denver, CO5 days ago$19.29 - $23 per hour
...of CPC. We are currently looking for a Research Assistant I in Colorado (USA). Join a dynamic... ...health outcomes through impactful clinical trials and community programs. This role... ...content Liaise with investigational sites and sponsors to resolve data queries and maintain up-...Hourly payFull timeTemporary workPart timeWork at officeLocal areaImmediate startRemote workWorldwideFlexible hoursShift workJobgether
Denver, CO4 days ago$60k - $70k
...people and grow your career in medical research? Minimally Invasive Procedure Specialists... ...disability Growth opportunities A dedicated mentor/apprentice program to fuel your career... ...Assistant, you will help coordinate clinical studies, manage grants, and take care of...Full timeTemporary workApprenticeshipWork at officeMonday to FridayMinimally Invasive Procedure Specialists
Littleton, CO4 days ago- ...least two years of experience, state licensure and BLS. Competitive and Transparent Pay We value your expertise and respect your dedication — and our goal is to compensate you more than fairly for them. We don't want you to scramble to figure out your coverage, especially...
Meda Health
Denver, CO4 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Associate, Sponsor Dedicated. Be the first to apply!
- on-site clinical research associate (traveling/remote) Denver, CO
- clinical trials assistant Denver, CO
- clinical research associate Denver, CO
- clinical research assistant Denver, CO
- clinical research associate cra Denver, CO
- clinical research administrator Denver, CO
- clinical research part time Denver, CO
- clinical trials Denver, CO
- clinical research regulatory Denver, CO
- clinical research manager remote Denver, CO