330 Results for

Medical Research Jobs in Central, CT

Jobs

Remote

$164,900–$226,750 / year

p>The Medical Affairs Research Manager will partner with multiple internal cross-functional stakeholders as well as external collaborators and clinical experts to identify clinical unmet need and evidence gaps to advance clinical feasibility, clinical validity, and other studies.

Primary Location: Remote-USA-CO Primary Location Base Pay Range: $164,900 - $226,750 Other US Location(s) Base Pay Range: $164,900 - $226,750 If the role is performed in Colorado, the pay range for this job is: $164,900 - $226,750.

30+ days ago

Littleton, CO

$60,000–$70,000 / year

With over four decades of combined experience and armed with cutting-edge technology, our clinic provides precise treatment for complex vascular and chronic conditions, including pelvic venous disorders, POTS, long COVID, and fibroids.

Our team at Minimally Invasive Procedure Specialists comprises world-renowned vascular specialists and healthcare support staff who are passionate about making a real difference in others' lives.

30+ days ago

Denver, CO

$65,574–$83,410 / year

Interpersonal Skills - Ability to establish and maintain effective working relationships with employees at all levels; interacts with people in a friendly, open, honest manner; models a commitment to teamwork; demonstrates respect for the opinions of others; and maintains high level of confidentiality. As a member of the research team this position is responsible for conducting key aspects of research for Phase I-IV industry-sponsored, co-operative group and or investigator-initiated clinical trials in accordance with the trial protocols, FDA Regulations, and ICH/GCP Guidelines.

30+ days ago

Littleton, Colorado

$60,000–$75,000 / year

Overview:

Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Clinical Research Coordinator/RN in Littleton.

Knowledge of medical terminology, nursing assessment, anatomy and physiology, clinical medical, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology, clinical trials and GCP concepts.

30+ days ago

Denver, Colorado

$60,000–$75,000 / year

Overview:

Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Clinical Research Coordinator/RN at our Midtown location in Denver.

21 days ago

Lone Tree, Colorado

$60,000–$75,000 / year

Overview:

21 days ago

Denver, CO

$50–$55 / hour

With interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation.

Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.

22 days ago

Virtual, CO

$70–$75 / hour

Enjoy the convenience of working remotely while having the opportunity to travel extensively across the United States, supporting groundbreaking clinical trials.

Responsibilities:
Monitor the progress of clinical trials at site level or headquarters, ensuring compliance with protocols, SOPs, GCP, and regulatory requirements.

30+ days ago

Aurora, CO

$49,899–$58,382 / year

If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively. Various trials in our office involve assessment of patient vascular function to evaluate the impact of a given intervention on CKD-related cardiovascular dysfunction and kidney disease progression.

12 days ago

Boulder County, Colorado

$100,000–$145,000 / year

However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. From early R&D, through complex regulatory approvals and into production, our global laboratory network of scientists, engineers, and technologists support customers to achieve assurance over product quality, sustainable outcomes, and market access.

25 days ago

Denver, CO

$58,705–$78,665 / year

This position is accountable for meeting study-specific goals and timelines, while also performing and assisting with clinical tasks related to study-specific tests, procedures, and treatments as assigned based on appropriate licensure and/or completion of competency documentation and team needs.

Why Join Us:

The Division of Gastroenterology and Hepatology in the Department of Medicine at the University of Colorado Anschutz Medical Campus is an internationally recognized program that provides comprehensive resources for the diagnosis and treatment of diseases of the digestive tract, pancreas, and liver.

24 days ago

Denver, Colorado

$87,000–$117,000 / year

Conduct protocol-specific training for study personnel to include training of staff in preparation for study activities Review protocols and provide input on study activities in relation to areas of May work with SRL to determine study recruitment and enrollment goals. Overview:

Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced QA Lead Clinical Research Coordinator/RN in Denver.

12 days ago

Denver, CO

$108,800–$202,000 / year

p>Relationship Management & Site Support: Builds deep, multi-stakeholder relationships at strategic sites (including investigators, pharmacists, and administration), acting as a "site champion" and Primary Point of Contact to maintain cross-study consistency and address site needs.

Cross-Functional Collaboration & Reporting: Partners seamlessly with internal teams (e.g., Medical Affairs, Study Start-Up) and CROs to ensure unified site communication, while maintaining meticulous documentation of site visits and interactions in central systems (e.g., Veeva).

20 days ago

Denver, CO

$74,422.15–$138,421.86 / year

Knowledge, Skills, and Abilities:

Identified ability to supervise clinical research teams, lead and accept responsibility, exercise authority, and function independently using effective written and verbal communication in English. Delivers effective and compliant clinical research study coordination, including planning, organizing, and managing all activities related to clinical research protocols.

12 days ago

Denver, CO

$50–$55 / hour

Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.

24 days ago

Denver, CO

$15–$25 / hour

li>Compile and prepare essential documents such as FDA forms, CVs, licensure, and IRB submission forms, obtaining all necessary signatures.

High School diploma required; certification as Medical Assistant or a bachelor’s degree in a health-related field (biology, public health, etc.) preferred.

30+ days ago

Englewood, CO

$59,000–$100,000 / hour

EXPERIENCE AND REQUIRED SKILLS: 2 to 4 years of clinical research experience, or has successfully performed in the role of Clinical Research Coordinator I for a minimum of 3 years and demonstrated outstanding performance through performance evaluations, certification and other job performance measures. Provides relevant information regarding the projected regional costs of treatments, projected enrollment capabilities, anticipated risks/benefits at specific study sites, logistical impediments, etc. for use in study contract and budget negotiations.

20 days ago

Aurora, CO

$60,000–$70,000 / year

This role works closely with Clinical Trial Managers (CTMs), Clinical Research Associates (CRAs), Clinical Operations Managers, and SEEV Specialists to ensure consistent site training, site engagement, data quality, and timely issue resolution, particularly for sites requiring additional operational support.

The Clinical & Endpoint Research Associate supports site operations with a primary focus on internal travel to complete Site Endpoint Evaluation Visits (SEEVs) and assists with enrollment and retention escalations for international sites.

30+ days ago

Boulder, CO

$90,000–$140,000 / year

Our intimate knowledge of muscle biology and biophysics along with our ability to identify and design muscle specific precision small molecules have enabled us to rapidly advance our skeletal muscle and cardiac muscle product candidates into the clinic while also building a robust pre-clinical pipeline.

Minimum 4 years of independent on-site monitoring experience (across all visit types and inclusive of remote monitoring), with at least 3 years cardiac study experience in a pharmaceutical sponsor environment preferred (global pharma or biotech preferred).

30+ days ago

Denver, CO

Preferred Qualifications: Bachelor's degree in science or health related field Three (3) years of clinical research or related experience Experience with electronic data capture systems (e.g., EMR or EHR and data management systems) Additional certification (one of the following): CCRC - Certified Clinical Research Coordinator CCRP - Certified Clinical Research Professional CCRA - Certified Clinical Research Associate Knowledge, Skills and Abilities: Knowledge and understanding of federal regulations and Good Clinical Practice (GCP) Ability to communicate effectively, both in writing and orally Ability to establish and maintain effective working relationships with employees at all levels throughout the institution Outstanding customer service skills Knowledge of basic human anatomy, physiology medical terminology Ability to interpret and master complex research protocol information How to Apply: For full consideration, please submit the following document(s): A letter of interest describing relevant job experiences as they relate to listed job qualifications and interest in the position (only use if a cover letter is necessary) Curriculum vitae / Resume Three to five professional references, including name, address, phone number (mobile number if appropriate), and email address Questions should be directed to: Kathy. The University of Colorado offers an excellent benefits package including: Medical: Multiple plan options Dental: Multiple plan options Additional Insurance: Disability, Life, Vision Retirement 401(a) Plan: Employer contributes 10% of your gross pay Paid Time Off: Accruals over the year Vacation Days: 22/year (maximum accrual 352 hours) Sick Days: 15/year (unlimited maximum accrual) Holiday Days: 10/year Tuition Benefit: Employees have access to this benefit on all CU campuses ECO Pass: Reduced rate RTD Bus and light rail service There are many additional perks & programs with the CU Advantage.

30+ days ago

Denver, CO

Collaborate with other clinical research team members, investigators, and hospital staff to ensure tests and procedures required by research protocols are performed and documented (e.g., vital signs, phlebotomy, specimen processing, electrocardiograms (EKGs), research drug administration, and protocol-specific tests and procedures); follow up with appropriate persons on missing or discrepant data. As the state''s only National Cancer Institute (NCI) designated Comprehensive Cancer Center, we hold a prestigious distinction that acknowledges our exceptional contributions to the fields of research, clinical trials, prevention, and cancer control.

30+ days ago

Denver, CO

$50,835.71–$94,545.54 / year

Additional Information: An equivalent combination of education and relevant work experience may be considered in lieu of the stated degree requirement: Bachelor's degree in healthcare or related field with no research experience OR. Maintains sensitivity to cost containment measures by conserving hospital supplies, equipment, and human resources while overseeing proposed project budgets from internal and external funding sources.

20 days ago

Virtual, CO

Remote

$40–$45 / hour

h3>Responsibilities:

Monitor clinical trial sites and ensure protocol/GCP/regulatory compliance.
Support study startup, monitoring, recruitment, and retention activities.

30+ days ago

Denver, CO

$58,705–$78,665 / year

p>The Clinical Research Support Team (CReST) has an opening for a full-time Clinical Research Startup Specialist to provide regulatory and operationalization startup support for a variety of interventional and observational studies conducted at the University of Colorado Anschutz Medical Campus and affiliate hospitals, including FDA regulated trials with industry, federal, and non-profit funding. If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively.

27 days ago

Denver, CO

$110,520–$138,150 / year

Willing and able to travel up to 50% for on-site monitoring visits across the West region; preference given to candidates residing in Los Angeles, Phoenix, Seattle, Denver or Portland, near major HUB airports to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

18 days ago

Englewood, CO

p>• 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.

30+ days ago

Denver, CO

$91,336–$114,170 / year

li>

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

18 days ago

$91,336–$114,170 / year

li>

Willing and able to travel up to 60% for on-site monitoring visits across the West region; preference given to candidates residing in West region near major HUB airports to support efficient regional travel.

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

30+ days ago

Littleton, Colorado

li style="margin-left:8px">Demonstrate superior patient relations and interpersonal skills; demonstrate an appropriate level of mental and emotional tolerance and even temperament when dealing with staff, patients and general public using tact, sensitivity and sound judgment; promote a positive work environment and contribute to the overall efforts of the department and the company. In addition, the ClinicalResearch Coordinator must be able to provide efficient services to our physicians as well as provide quality, courteous and compassionate services to our patients in adherence to the guidelines, policies and procedures set forth by Urology Associates.

19 days ago

Denver, CO

p>• Engage in clinical trial management on a day to day level; • Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy; • Compile and maintain project-specific status reports; • Interact with the Sponsor, study sites, and internal associates; • Provide oversight and quality control of our internal regulatory filing system; • Manage study supplies; • Create and maintain project timelines; • Coordinate project meetings and produce quality meeting minutes.

Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Structured career paths with opportunities for professional growth Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center RTD Eco Pass Secure bike storage room Awards.

30+ days ago

Denver, CO

$19.31–$26.22 / hour

Frequent interactions with providers, colleagues, customers, patients/clients, and visitors that require employee to verbally communicate as well as hear and understand spoken information, needs, and issues quickly and accurately. The following will be done under direct supervision: Credential Management: Support onboarding for new research staff by preparing, collecting, and filing "research ready" documents in compliance with required training and applicable regulations.

17 days ago

Aurora, CO

$50,175–$63,823 / year

The campus encompasses the University of Colorado health professional schools, more than 60 centers and institutes, and two nationally ranked independent hospitals - UCHealth University of Colorado Hospital and Children''s Hospital Colorado - that treat more than two million adult and pediatric patients each year. Innovative, interconnected and highly collaborative, the University of Colorado Anschutz Medical Campus delivers life-changing treatments, patient care and professional training and conducts world-renowned research fueled by over $650 million in research grants.

30+ days ago

p>What We Are Searching For:

Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required.
Responsible for the validity, correctness, and completeness of the clinical data reviewed and collected at assigned sites as dictated by ICH GCP/ISO14155, protocol and client requirements.

30+ days ago

Denver, Colorado

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• Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks.

26 days ago

Lafayette, CO

p>The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

30+ days ago

Denver, Colorado

Responsibilities :

Engage in clinical trial management on a day to day level;
Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy;
Compile and maintain project-specific status reports;
Interact with the Sponsor, study sites, and internal associates;
Provide oversight and quality control of our internal regulatory filing system;
Manage study supplies;
Create and maintain project timelines; and.
.

30+ days ago

Denver, CO

$25,560.50–$32,572.50 / year

Our team brings together experts in developmental-behavioral pediatrics, endocrinology, genetic counseling, psychology, neuropsychology, cardiology, nephrology, otolaryngology, audiology, sleep medicine, speech and occupational therapy, nursing, and social work, alongside research service professionals and trainees. If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively.

30+ days ago

Aurora, CO

$49,899–$66,865 / year

The research group consists of multiple physician investigators, research coordinators and laboratory personnel engaging primarily in federally funded research to improve care and outcomes for hospitalized and community-based patients, including participants with Long COVID and ICU survivors returning after their illness to the Anschutz Medical Campus.

Job Summary:

The Division of Pulmonary Sciences and Critical Care Medicine is seeking an energetic individual for a full-time Research Services Professional for inpatient and outpatient research projects evaluating physical, emotional, and psychological recovery after critical illness and COVID-19 infection.

30+ days ago

Lakewood, Colorado

div>

Medical Research Jobs in Central, CT

Responsibilities:
Monitor the progress of clinical trials at site level or headquarters, ensuring compliance with protocols, SOPs, GCP, and regulatory requirements.

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Medical Research Jobs in Central, CT

Medical Affairs Research Manager Guardant Health Inc

Clinical Research Coordinator Minimally Invasive Procedure Specialists

Clinical Research Nurse University of Colorado

Clinical Research Coordinator/RN Rocky Mountain Cancer Centers

Clinical Research Patient Coordinator Rocky Mountain Cancer Centers

Clinical Research Coordinator Rocky Mountain Cancer Centers

Per Diem Clinical Research Nurse - Home Visits Science 37

Clinical Research Monitor(CRA) LanceSoft Inc

Responsibilities: Monitor the progress of clinical trials at site level or headquarters, ensuring compliance with protocols, SOPs, GCP, and regulatory requirements.

Open Rank Clinical Research Coordinator (Entry - Senior) University of Colorado

Clinical Research Manager Element Materials Technology

Clinical Research SURVENT Project Coordinator University of Colorado

QA Lead Clinical Research/RN Rocky Mountain Cancer Centers

Clinical Research Engagement Lead - West Region (Denver, CO) Genentech Inc

Supv, Clinical Research RN Oncology AdventHealth

Per Diem Clinical Research Nurse - Home Visits Science 37 Inc

Research Assistant (part-time) Joulé

Clinical Research Coordinator II Fresenius Medical Care AG & Co KGaA

Clinical & Endpoint Research Associate CPC Clinical Research

Senior Clinical Research Associate - Cardiovascular (EDG-2026033) Edgewise Therapeutics Inc

Clinical Research Coordinator (Melanoma/RT Team) University of Colorado

Clinical Research Coordinator (Lung Team) University of Colorado

Clinical Research Coordinator I Exempt AdventHealth

Clinical Research Monitor(CRA) Artech LLC

Clinical Research Startup Specialist University of Colorado

Senior Clinical Research Associate ICON Plc

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

Clinical Research Associate II ICON Plc

Clinical Research Associate ICON Plc

Clinical Research Coordinator - Urology Associates Denver

Senior Clinical Research Project Coordinator Denver Medpace Holdings Inc

Research Assistant Regulatory Credentialing Intermountain Health Inc

Clinical - Research Services Entry Professional University of Colorado

Clinical Research Associate I (Central: IL, CO, MI, KS, TN) Premier Research International LLC

Clinical Research Associate II - Oncology & Neurology (WA, OR, ID, MT, WY, CO) Thermo Fisher Scientific

Prin Clinical Research Spec Medtronic Plc

Senior Clinical Research Project Coordinator - Denver Medpace, Inc.

Clinical Research Data Specialist (Part-time to Full-time) University of Colorado

Open Rank Research Services Clinical Sciences Professional (Entry - Intermediate) University of Colorado

Research Coordinator ADVU Advanced Urology C

Clinical Research Manager Element Materials Technology Group Ltd

Research Services Professional (Intermediate or Senior) University of Colorado

Open Rank Clinical Research Coordinator (Entry - Intermediate) University of Colorado

Clinical Trials Research Coverage Analyst University of Colorado Health

Research Services Senior Professional / Senior Clinical Sciences Professional University of Colorado

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Research Assistant (part-time) System One

Senior Clinical Research Coordinator Flourish Research

Research Services Clinical Sciences Professional OPEN RANK (Intermediate - Senior) University of Colorado

MRC Clinical Science Senior Research Professional University of Colorado

Oncology Clinical Research Coordinator-RN AdventHealth

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Responsibilities:
Monitor the progress of clinical trials at site level or headquarters, ensuring compliance with protocols, SOPs, GCP, and regulatory requirements.