Mid Level Study Start Up Jobs
Mid level study start up jobs go to professionals ready to own study startup workflows end to end, guide junior coordinators, and make protocol decisions with limited oversight. Openings across Healthcare & Medical Services and Biotechnology & Pharmaceuticals are posted by employers like Medpace, with 20% of roles offered remotely or hybrid, hiring at this level now.
Find Mid Level Study Start Up JobsOverview
Showing 5 of 5+ Mid Level Study Start Up jobs
Looking for more mid level study start up jobs?
Explore related role searches to find more openings that fit.
See related jobsDo you enjoy working in a fast-paced environment where you are empowered to make strategic decisions and contribute to a growing and profitable company? Join us at Medpace! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace.
Incentives can include: Competitive bonus program, sign-on bonus, and equity awards.
Location: Remote
Responsibilities
- Efficiently manage successful execution of global start-up, maintenance, and close-out studies;
- Effectively lead others in a matrix environment;
- Perform quality checks on submission documents and site essential documents;
- Prepare and approve informed consent forms;
- Serve as a Sponsor point of contact for start-up and regulatory submissions items;
- Review pertinent regulations to develop proactive solutions to start-up challenges;
- Prepare new business proposals and present during bid defenses, general capabilities meetings, and audits;
- Contribute to the growth and development of departmental staff, processes and systems.
Qualifications
- Bachelor's degree required, advanced degree in Life Sciences preferred
- 5+ years of experience in clinical research, preferably in a Senior/Lead role at a CRO in Study Start-Up
- Project management experience and demonstrated role in developing others
- Strong oral and written communication skills required
Travel: Minimal
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 5,000 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.
Medpace Perks
- Flexible work environment
- Competitive PTO packages – starting at 20+ days
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Competitive compensation and benefits package
- Structured career paths with opportunities for professional growth
- Discounts for local businesses
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.
Do you enjoy working in a fast-paced environment where you are empowered to make strategic decisions and contribute to a growing and profitable company? Join us at Medpace! Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, Global Study Start-Up Project Manager to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace.
Incentives can include: Competitive bonus program, sign-on bonus, and equity awards.
Location: Remote
Responsibilities
- Efficiently manage successful execution of global start-up, maintenance, and close-out studies;
- Effectively lead others in a matrix environment;
- Perform quality checks on submission documents and site essential documents;
- Prepare and approve informed consent forms;
- Serve as a Sponsor point of contact for start-up and regulatory submissions items;
- Review pertinent regulations to develop proactive solutions to start-up challenges;
- Prepare new business proposals and present during bid defenses, general capabilities meetings, and audits;
- Contribute to the growth and development of departmental staff, processes and systems.
Qualifications
- Bachelor's degree required, advanced degree in Life Sciences preferred
- 5+ years of experience in clinical research, preferably in a Senior/Lead role at a CRO in Study Start-Up
- Project management experience and demonstrated role in developing others
- Strong oral and written communication skills required
Travel: Minimal
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 5,000 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.
Medpace Perks
- Flexible work environment
- Competitive PTO packages – starting at 20+ days
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Competitive compensation and benefits package
- Structured career paths with opportunities for professional growth
- Discounts for local businesses
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.
See All 5 Mid Level Study Start Up Jobs
Find roles that match your experience and apply in just a few clicks.
Find Mid Level Study Start Up JobsMid Level Study Start Up Job Market
Who's Hiring
Top Industries Hiring
- Healthcare & Medical Services
- Biotechnology & Pharmaceuticals
Mid Level Study Start Up Jobs: Frequently Asked Questions
How do I get a mid level study start up job?
Position yourself as someone who has owned a complete startup deliverable, not just supported one. Highlight experience coordinating site activation, managing vendor relationships, or leading regulatory submissions without constant oversight. Applications that name specific protocols you have managed, therapeutic areas you know well, and cross-functional teams you have worked alongside stand out to hiring managers at this level.
Which companies hire mid level study start ups?
Companies hiring mid level study start ups right now include Medpace, based on current listings on Migrate Mate as of August 2026. Hiring at this level comes from a mix of contract research organizations, pharmaceutical sponsors, and specialized clinical operations firms that need professionals who can manage site portfolios independently.
Are there remote mid level study start up jobs?
Yes, remote and hybrid arrangements are common at this experience level. About 20% of mid level study start up openings are remote or hybrid as of August 2026, reflecting an industry shift toward distributed clinical operations teams. Roles focused on document management, regulatory coordination, and vendor oversight tend to offer the most location flexibility.
How do I move up to a mid level study start up role?
Growth into mid level comes from building depth in a specific phase of the startup process, whether that is feasibility, site qualification, or IRB submission, and then taking measurable ownership of outcomes. Professionals who demonstrate they can manage a site from activation to enrollment independently, document lessons learned, and mentor newer coordinators consistently make the jump from entry level to mid level within a few years.
Which industries hire the most mid level study start ups?
Mid Level study start up roles concentrate in Healthcare & Medical Services and Biotechnology & Pharmaceuticals, based on current listings on Migrate Mate as of August 2026. Those sectors drive demand because they run large, multi-site trials that require experienced professionals who can manage startup timelines and regulatory requirements without step-by-step guidance.