Science & Research STEM OPT Jobs in Colorado
Science and research F-1 STEM OPT sponsorship jobs in Colorado are concentrated around Denver, Boulder, and Fort Collins, where institutions like the National Renewable Energy Laboratory, the University of Colorado system, and biotech employers such as Colotech and Charles River Laboratories actively hire STEM OPT candidates in life sciences, environmental research, and applied physics roles.
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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). 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.
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.
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). 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.
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.
STEM OPT Science & Research Job Roles in Colorado
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Search Science & Research Jobs in ColoradoScience & Research STEM OPT Sponsorship Jobs in Colorado: Frequently Asked Questions
Which science and research companies sponsor F-1 STEM OPT visas in Colorado?
Colorado employers with documented STEM OPT sponsorship activity in science and research include the National Renewable Energy Laboratory in Golden, Ball Aerospace in Broomfield, Leidos, Charles River Laboratories, and several University of Colorado affiliated research centers. Biotech and environmental science firms in the Denver-Boulder corridor also appear consistently in DOL Labor Condition Application filings for STEM-related occupations.
Which cities in Colorado have the most science and research F-1 STEM OPT sponsorship jobs?
Boulder and Denver account for the largest concentration of science and research STEM OPT sponsorship opportunities in Colorado. Boulder hosts a dense cluster of federal research labs, clean energy firms, and atmospheric science organizations. Fort Collins supports agricultural and environmental research through Colorado State University affiliates, while the Denver metro attracts aerospace, defense science, and life sciences employers with active sponsorship histories.
What types of science and research roles typically qualify for F-1 STEM OPT sponsorship in Colorado?
Roles that commonly qualify include research scientist, data scientist, computational biologist, environmental scientist, materials scientist, atmospheric researcher, and laboratory analyst positions. Qualifying roles must align with a STEM-designated degree field recognized by USCIS. Colorado employers frequently sponsor positions in clean energy research, aerospace science, climate science, and biopharmaceutical research, provided the job duties directly relate to the candidate's degree program.
How do I find science and research F-1 STEM OPT sponsorship jobs in Colorado?
Migrate Mate filters science and research jobs in Colorado specifically by F-1 STEM OPT sponsorship eligibility, surfacing employers with verified DOL Labor Condition Application filing history in STEM occupations. This saves time compared to manually reviewing employer records. You can filter by location, role type, and visa category to find positions in Boulder, Denver, Fort Collins, and other Colorado research hubs where active sponsorship is confirmed.
Are there state-specific considerations for F-1 STEM OPT sponsorship in science and research roles in Colorado?
Colorado has a strong federally funded research presence, meaning several major employers are government contractors or national laboratories. These organizations sometimes have additional hiring requirements, including security clearance eligibility, which can affect international candidates. Separately, STEM OPT authorization requires your employer to be enrolled in E-Verify and your role to appear on USCIS's list of STEM-designated degree programs, regardless of state.