Clinical Research Director Jobs at Medpace with Visa Sponsorship
Medpace hires Clinical Research Directors to lead full-service clinical trial execution across therapeutic areas, and the company has a consistent track record of sponsoring work visas for qualified candidates in this function. If you're an international professional targeting this role, Medpace is a serious path worth pursuing.
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Get Access To All JobsJOB SUMMARY
Medpace is continuing to add experienced CTM Directors and Sr. Project Managers to join our Clinical Trial Management Group to office in Denver, CO. This position will be responsible for mentoring CTMs as well as overseeing projects and sponsor relationships. Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience, and more. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.
This position is a full-time office-based role in our Denver, CO office, with some work-from-home flexibility following tenure with the company.
Responsibilities
- Mentor Clinical Trial Managers, Project Coordinators, and other study team members in the Denver, CO office
- Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
- Serve as primary Sponsor contact for operational project-specific issues and study deliverables
- Maintain in depth knowledge of protocol, therapeutic area, and indication
- Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
- Develop operational project plans
- Manage risk assessment and execution
- Manage study vendors where applicable
- Manage site quality and monitoring deliverables
- Work collaboratively with HR to support recruitment of new staff in Denver office
- Serve as an escalation point for Clinical Operations in the Denver office
- Implement and support Medpace corporate strategies in Denver office
- Organize a cross-functional leadership team to align and support all associates in the Denver office.
BASIC QUALIFICATIONS
- Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred
- Experience in Phases 1-4; Phases 2-3 preferred
- 5+ years as a project/clinical trial manager within a CRO
- Management of overall project timeline
- Bid defense experience
- Strong leadership skills
COMPENSATION
A target salary range of $175,000 - $250,000 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 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.
DENVER PERKS
Denver Office Overview
- 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
- 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 continuing to add experienced CTM Directors and Sr. Project Managers to join our Clinical Trial Management Group to office in Denver, CO. This position will be responsible for mentoring CTMs as well as overseeing projects and sponsor relationships. Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience, and more. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.
This position is a full-time office-based role in our Denver, CO office, with some work-from-home flexibility following tenure with the company.
Responsibilities
- Mentor Clinical Trial Managers, Project Coordinators, and other study team members in the Denver, CO office
- Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
- Serve as primary Sponsor contact for operational project-specific issues and study deliverables
- Maintain in depth knowledge of protocol, therapeutic area, and indication
- Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
- Develop operational project plans
- Manage risk assessment and execution
- Manage study vendors where applicable
- Manage site quality and monitoring deliverables
- Work collaboratively with HR to support recruitment of new staff in Denver office
- Serve as an escalation point for Clinical Operations in the Denver office
- Implement and support Medpace corporate strategies in Denver office
- Organize a cross-functional leadership team to align and support all associates in the Denver office.
BASIC QUALIFICATIONS
- Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred
- Experience in Phases 1-4; Phases 2-3 preferred
- 5+ years as a project/clinical trial manager within a CRO
- Management of overall project timeline
- Bid defense experience
- Strong leadership skills
COMPENSATION
A target salary range of $175,000 - $250,000 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 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.
DENVER PERKS
Denver Office Overview
- 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
- 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.
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Get Access To All JobsTips for Finding Clinical Research Director Jobs at Medpace Jobs
Align your credentials to Medpace's therapeutic focus
Medpace specializes in oncology, cardiology, and metabolic disease trials. Frame your CV around therapeutic area depth and protocol leadership in those spaces, not just general CRO experience. Reviewers here distinguish between trial oversight and genuine scientific direction.
Target Medpace's Cincinnati headquarters strategically
A significant share of Medpace's Clinical Research Director openings are based at their Cincinnati campus. If you're on OPT or need a timely H-1B transfer, applying to roles tied to that hub can simplify the filing process and reduce multi-site coordination delays.
Clarify your visa status early in the process
Medpace runs structured interview pipelines for director-level roles. Raise your visa situation before the final offer stage, not after. Confirming whether you need H-1B transfer, cap-exempt filing, or a new petition saves both parties from late-stage surprises.
Understand how TN status applies to your background
If you're a Canadian or Mexican national with a qualifying science or research degree, TN status can get you into a Clinical Research Director role faster than H-1B sponsorship. DOL's TN occupation list covers several categories relevant to clinical research scientists.
Prepare for PERM if a Green Card path matters to you
For EB-2 or EB-3 sponsorship, Medpace must demonstrate through DOL's PERM process that no qualified U.S. worker is available. Director-level roles can satisfy this more cleanly than generalist positions, but timelines from PERM filing to priority date can stretch beyond two years.
Use Migrate Mate to surface open roles efficiently
Clinical Research Director openings at Medpace aren't always posted consistently across job boards. Use Migrate Mate to filter specifically for Medpace roles that include visa sponsorship, so you're applying to verified positions rather than guessing from incomplete listings.
Clinical Research Director at Medpace jobs are hiring across the US. Find yours.
Find Clinical Research Director at Medpace JobsFrequently Asked Questions
Does Medpace sponsor H-1B visas for Clinical Research Directors?
Yes, Medpace sponsors H-1B visas for Clinical Research Directors. The role qualifies as a specialty occupation given the degree requirements in clinical, scientific, or regulatory fields. If you're already on an H-1B with another employer, Medpace can file an H-1B transfer petition, which allows you to start working as soon as the transfer is filed and receipt is received.
How do I apply for Clinical Research Director jobs at Medpace?
Applications go through Medpace's careers portal at medpace.com. Most Clinical Research Director listings require you to submit a resume and complete a short application form. You can also find verified Medpace openings that include visa sponsorship by browsing through Migrate Mate, which filters specifically for roles open to international candidates needing work authorization.
Which visa types are commonly used for Clinical Research Director roles at Medpace?
The most common visa categories for this role at Medpace are H-1B, TN (for Canadian and Mexican nationals with qualifying degrees), and F-1 OPT for candidates completing graduate programs in clinical or life sciences. For candidates seeking permanent residence, Medpace has sponsored EB-2 and EB-3 Green Cards through the PERM labor certification process for director-level positions.
What qualifications does Medpace expect for Clinical Research Director candidates?
Medpace typically expects a graduate degree in a clinical, scientific, or health-related field alongside substantial experience managing Phase II or Phase III trials from protocol development through regulatory submission. Therapeutic area expertise in oncology, cardiology, or metabolic disease carries significant weight. Candidates who have led cross-functional teams and interfaced directly with sponsors are consistently prioritized over those with purely operational backgrounds.
How do I estimate the timeline from job offer to work authorization at Medpace?
Timeline depends on your visa category. An H-1B transfer from an existing petition can take two to four weeks for USCIS receipt, with work authorization available immediately upon filing. A new H-1B cap subject petition requires waiting for the next October 1 start date. TN status for Canadian nationals can be obtained at the border in a single day. OPT authorization is already in place before the offer, so there's no additional USCIS filing required.
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