CO · Hybrid
Study Start-Up/Regulatory Submissions experience within a CRO is required. Incentives can include: Competitive bonus program, sign-on/relocation bonus, and equity awards. Location: Position can be ...
CO · Hybrid
Study Start-Up/Regulatory Submissions experience within a CRO is required. Incentives can include: Competitive bonus program, sign-on/relocation bonus, and equity awards. Location: Position can be ...
Experienced Study Start-Up Research Coordinator
Denver, CO · On-site
$40K - $100K/yr
Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Experienced Study Start-Up Research Coordinator
Denver, CO · On-site
$40K - $100K/yr
Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Experienced Study Start-Up Research Coordinator
Denver, CO · Hybrid
$40K - $100K/yr
Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
Experienced Study Start-Up Research Coordinator
Denver, CO · Hybrid
$40K - $100K/yr
Maintain timelines for study start-up through both internal and external collaboration; * Provide ... associates, as well as those that are new to the industry. The SAM Training Program embraces ...
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Clinical Research Associate
Denver, CO · On-site
Senior Clinical Research Associate As Clinical Research Associate you will be responsible for ... Works with Study Start-up Group and site staff to obtain regulatory (IRB/EC) approval of study ...
Quick apply
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Clinical Research Associate
Denver, CO · On-site
Senior Clinical Research Associate As Clinical Research Associate you will be responsible for ... Works with Study Start-up Group and site staff to obtain regulatory (IRB/EC) approval of study ...
Be Seen First
Clinical Research Associate
Denver, CO · On-site
Senior Clinical Research Associate As Clinical Research Associate you will be responsible for ... Works with Study Start-up Group and site staff to obtain regulatory (IRB/EC) approval of study ...
Quick apply
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Clinical Research Associate
Denver, CO · On-site
Senior Clinical Research Associate As Clinical Research Associate you will be responsible for ... Works with Study Start-up Group and site staff to obtain regulatory (IRB/EC) approval of study ...
Research Coordinator
Greeley, CO · On-site
This role will coordinate day-to-day research operations for faculty and students; facilitate compliant and efficient study start-up and execution; maintain research documentation and reporting; and ...
Research Coordinator
Greeley, CO · On-site
This role will coordinate day-to-day research operations for faculty and students; facilitate compliant and efficient study start-up and execution; maintain research documentation and reporting; and ...
This role will coordinate day-to-day research operations for faculty and students; facilitate compliant and efficient study start-up and execution; maintain research documentation and reporting; and ...
This role will coordinate day-to-day research operations for faculty and students; facilitate compliant and efficient study start-up and execution; maintain research documentation and reporting; and ...
Research Coordinator
Greeley, CO · On-site
$57K - $65K/yr
This role will coordinate day-to-day research operations for faculty and students; facilitate compliant and efficient study start-up and execution; maintain research documentation and reporting; and ...
Research Coordinator
Greeley, CO · On-site
$57K - $65K/yr
This role will coordinate day-to-day research operations for faculty and students; facilitate compliant and efficient study start-up and execution; maintain research documentation and reporting; and ...
Manage all clinical study project elements from initiation to close-out with an emphasis on study start-up ensuring training and education of investigators and research staff. * Work collaboratively ...
New
Manage all clinical study project elements from initiation to close-out with an emphasis on study start-up ensuring training and education of investigators and research staff. * Work collaboratively ...
New
Senior Manager, Clinical Operations
$146K - $210K/yr
Manage all clinical study project elements from initiation to close-out with an emphasis on study start-up ensuring training and education of investigators and research staff. * Work collaboratively ...
Senior Manager, Clinical Operations
$146K - $210K/yr
Manage all clinical study project elements from initiation to close-out with an emphasis on study start-up ensuring training and education of investigators and research staff. * Work collaboratively ...
Senior Manager, Clinical Operations
$146K - $210K/yr
Manage all clinical study project elements from initiation to close-out with an emphasis on study start-up ensuring training and education of investigators and research staff. * Work collaboratively ...
Quick apply
Senior Manager, Clinical Operations
$146K - $210K/yr
Manage all clinical study project elements from initiation to close-out with an emphasis on study start-up ensuring training and education of investigators and research staff. * Work collaboratively ...
Senior Clinical Research Coordinator
Denver, CO · On-site
$70K - $85K/yr
Support study start-up and planning, including PSVs and SIVs * Support IRB submission and correspondence * Facilitate monitoring visits (IMVs) and sponsor correspondence including managing the ...
Quick apply
Senior Clinical Research Coordinator
Denver, CO · On-site
$70K - $85K/yr
Support study start-up and planning, including PSVs and SIVs * Support IRB submission and correspondence * Facilitate monitoring visits (IMVs) and sponsor correspondence including managing the ...
... study start-up, invoicing and close-out, and the growth and maintenance of the clinical research infrastructure for the organization. The Director is responsible for developing and overseeing ...
... study start-up, invoicing and close-out, and the growth and maintenance of the clinical research infrastructure for the organization. The Director is responsible for developing and overseeing ...
Clinical Research Nurse D
Denver, CO · On-site
$75K - $104K/yr
... for study start up * Manage scheduling and coordination of subject study specified treatment, follow-up visits and procedures. Manage collection of data from source documents pertaining to study ...
Clinical Research Nurse D
Denver, CO · On-site
$75K - $104K/yr
... for study start up * Manage scheduling and coordination of subject study specified treatment, follow-up visits and procedures. Manage collection of data from source documents pertaining to study ...
Clinical Research Nurse D
$75K - $104K/yr
... for study start up * Manage scheduling and coordination of subject study specified treatment, follow-up visits and procedures. Manage collection of data from source documents pertaining to study ...
Clinical Research Nurse D
$75K - $104K/yr
... for study start up * Manage scheduling and coordination of subject study specified treatment, follow-up visits and procedures. Manage collection of data from source documents pertaining to study ...
$26 - $34.50/hr
Communication and coordination with the lead study team at the Longwood campus for study start-up, ongoing study team meetings, and project management of all site study activities * Responsible for ...
$26 - $34.50/hr
Communication and coordination with the lead study team at the Longwood campus for study start-up, ongoing study team meetings, and project management of all site study activities * Responsible for ...
CReST provides a la carte support services to clinical investigators for all activities related to the successful conduct of clinical research, from study start-up through close out. This is the ...
CReST provides a la carte support services to clinical investigators for all activities related to the successful conduct of clinical research, from study start-up through close out. This is the ...
Senior Manager, Clinical Operations
Westminster, CO · On-site +1
$146K - $210K/yr
Manage all clinical study project elements from initiation to close-out with an emphasis on study start-up ensuring training and education of investigators and research staff. * Work collaboratively ...
Senior Manager, Clinical Operations
Westminster, CO · On-site +1
$146K - $210K/yr
Manage all clinical study project elements from initiation to close-out with an emphasis on study start-up ensuring training and education of investigators and research staff. * Work collaboratively ...
... study start-up and close-out. Team Collaboration (20%) * Communicate and collaborate with various colleagues (e.g., principal investigator, clinicians, medical staff, sponsors, contract research ...
... study start-up and close-out. Team Collaboration (20%) * Communicate and collaborate with various colleagues (e.g., principal investigator, clinicians, medical staff, sponsors, contract research ...
... study start-up and close-out. Team Collaboration (20%) * Communicate and collaborate with various colleagues (e.g., principal investigator, clinicians, medical staff, sponsors, contract research ...
... study start-up and close-out. Team Collaboration (20%) * Communicate and collaborate with various colleagues (e.g., principal investigator, clinicians, medical staff, sponsors, contract research ...
Study Start Up Associate information
See Colorado salary details
$13.40 - $17.46
3% of jobs
$17.46 - $21.53
18% of jobs
$22.33 is the 25th percentile. Wages below this are outliers.
$21.53 - $25.60
20% of jobs
The median wage is $28.07 / hr.
$25.60 - $29.67
15% of jobs
$29.67 - $33.73
11% of jobs
$33.73 - $37.80
4% of jobs
$41.26 is the 75th percentile. Wages above this are outliers.
$37.80 - $41.87
5% of jobs
$41.87 - $45.93
8% of jobs
$45.93 - $50
6% of jobs
$50 - $54.07
6% of jobs
$54.07 - $58.14
3% of jobs
$13
$33
$58
How much do study start up associate jobs pay per hour?
As of Jul 7, 2026, the average hourly pay for study start up associate in Colorado is $33.16, according to ZipRecruiter salary data. Most workers in this role earn between $22.26 and $43.75 per hour, depending on experience, location, and employer.
What is the difference between Study Start Up Associate vs Clinical Trial Coordinator?
| Aspect | Study Start Up Associate | Clinical Trial Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, knowledge of regulatory requirements | Bachelor's degree, familiarity with clinical procedures |
| Work Environment | Regulatory and site initiation activities | Participant management and site coordination |
| Employer & Industry Usage | Pharmaceuticals, biotech, CROs | Hospitals, research centers, CROs |
The Study Start Up Associate primarily focuses on regulatory submissions, site qualification, and initiation processes, ensuring trial readiness. In contrast, the Clinical Trial Coordinator manages participant recruitment, scheduling, and data collection. Both roles are essential in clinical research but differ in their core responsibilities and focus areas.
What are popular job titles related to Study Start Up Associate jobs in Colorado? For Study Start Up Associate jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Study Start Up Associate jobs in Colorado look for? The top searched job categories for Study Start Up Associate jobs in Colorado are:
Other
Medical, PTO
Posted 28 days ago
Medpace rating
8.5
Based on 9 frontline employees who took The Breakroom Quiz
12th of 58 rated research
Job description
Job Summary
We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position will be an integral part of the Clinical Operations leadership team and requires a strong understanding of how study start-up and regulatory submissions are integrated with other clinical operations functions throughout Medpace. Study Start-Up/Regulatory Submissions experience within a CRO is required.
Incentives can include: Competitive bonus program, sign-on/relocation bonus, and equity awards.
Location: Position can be office based in Cincinnati, Dallas or Denver.
Responsibilities- Contribute directly to the growth and strategic development of a large, global Study Start-Up team;
- Develop and identify continuous improvement opportunities of internal processes;
- Oversee Study Start-Up/Regulatory Submissions activities and timelines to ensure they are in accordance with Medpace standard operating procedures and study protocols;
- Provide input on new business development opportunities; and
- Develop and maintain relationships with clients.
- Bachelor's degree in Life Sciences or related field, Advanced degree is preferred;
- 8+ years as a study start-up senior leader within a CRO;
- Excellent presentation, negotiation, documentation, leadership, team-orientation, and interpersonal skills;
- Strong customer focus with ability to manage challenging priorities and remain flexible and adaptive in stressful situations;
- Excellent written and oral communication; and
- Experience managing and developing a team.
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Cincinnati Perks
- 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
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Structured career paths with opportunities for professional growth
- Discounted tuition for UC online programs
Awards
Named a Top Workplace in 2024 by The Cincinnati Enquirer
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Employment Type: OTHER
About Medpace
Sourced by ZipRecruiter
Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Cincinnati, OH, US
Year founded
1992