Top 9 Clinical trial administrator Jobs in Colorado

Associate Clinical Trial Manager - PhD - Metabolic - Denver, CO
Medpace, Inc. —Denver, CO
- $70,000 - $90,000 a year
- Full-time
- Word processing
- English
- Mid-level
- Travel reimbursement
- AD&D insurance
Open Rank Clinical Trials Coordinator (Intermediate – Senior)
University of Colorado —Aurora, CO
- $54,302 - $74,665 a year
- Overtime
- Background check
- Anatomy knowledge
- Vital signs
- Disability insurance
- Health insurance
Senior Financial Analyst, Grants Administration (Clinical Trials Services)
Denver Health —Denver, CO
- $76,100 - $114,200 a year
- Full-time
- Customer service
- Pass drug screening
- Mid-level
- Paid parental leave
- Paid holidays
Clinical Trials, Business Development Representative
Milestone One —Model, CO
- Full-time
- Microsoft Excel
- Microsoft Outlook
- English
Quick Apply
Physician - Clinical Trials - MD/DO
Headlands Research —Colorado Springs, CO
- Part-time
- Medicine
- Management
- BC/BE
- Flexible schedule
- Life insurance
Drug Supply/Clinical Trial Supply Manager
CPC Clinical Research —Aurora, CO
- $70,000 - $90,000 a year
- Full-time
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Paid holidays
- Disability insurance
Quick Apply
1678: Administrative Assistant – Clinical Trials Support OMM
Colorado State University —Fort Collins, CO
- $50,000 - $56,000 a year
- Full-time
- Hybrid work
- Background check
- Microsoft Excel
- Microsoft Outlook
1d
Office of Clinical Trials (OCT) Coordinator
University of Colorado —Aurora, CO
- $56,995 - $72,498 a year
- Overtime
- Hybrid work
- Background check
- Microsoft Excel
- Microsoft Outlook
- Disability insurance
- Health insurance

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Associate Clinical Trial Manager - PhD - Metabolic - Denver, CO

Medpace, Inc. -
Denver, CO

Apply Now

Job Details

Full-time
$70,000 - $90,000 a year

Benefits

Travel reimbursement
AD&D insurance
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Paid time off
Food allowance
Work from home
Vision insurance
Opportunities for advancement
Pet insurance

Qualifications

Word processing
English
Windows
Doctor of Philosophy

Full Job Description

Job Summary:

Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience within Metabolic research for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities within Endocrine & Metabolic trials. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.

This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

Responsibilities :

Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager;
Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy;
Compile and maintain project-specific status reports within the clinical trial management system;
Interact with the internal project team, Sponsor, study sites, and third-party vendors;
Provide oversight and quality control of our internal regulatory filing system;
Provide oversight and management of study supplies;
Create and maintain project timelines; and
Coordinate project meetings and produce quality minutes.

Qualifications :

PhD in Life Sciences;
Expertise related to obesity, diabetes, MASH, MAFLD, hypoglycemia, or rare endocrine and metabolic diseases
Fluency in English with solid presentation skills;
Ability to work in a fast-paced dynamic industry within an international team;
Prior experience within the CRO or pharmaceutical industry not required but will be advantageous; and
Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.

Compensation

A target salary range of $70,000 - $90,000 with potential for bonus and equity awards. Your compensation will be based on your skills and experience. Medpace offers the following benefits for full-time positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, pet insurance, and reimbursement for travel expenses (including food and gas allowance, rental cars, and hotel accommodations). Applications will be accepted on an ongoing basis. For more details, please discuss with your recruiter.

Medpace Overview :

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?:

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

- Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

- Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

- Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

Apply Now

Refine Your Search

clinical trial administrator jobs in colorado

Associate Clinical Trial Manager - PhD - Metabolic - Denver, CO

Open Rank Clinical Trials Coordinator (Intermediate – Senior)

Senior Financial Analyst, Grants Administration (Clinical Trials Services)

Clinical Trials, Business Development Representative

Physician - Clinical Trials - MD/DO

Drug Supply/Clinical Trial Supply Manager

1678: Administrative Assistant – Clinical Trials Support OMM

Office of Clinical Trials (OCT) Coordinator

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