Clinical Research Director Jobs at Medpace with Visa Sponsorship
Clinical Research Director jobs at Medpace 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:
Our European clinical activities are growing rapidly, and we are currently seeking full-time, home-based Clinical Research Associates to join our Clinical Monitoring team, in the country of Georgia.
This position will be instrumental in growing the team in Georgia and accomplishing tasks and projects that are vital to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
The Clinical Research Associate at Medpace is offered the unique opportunity to be involved at every stage of the drug development process by providing unrivalled support to our customers. If you want an exciting career where you use your medical or health background and education, travel extensively and are instrumental in the clinical trials process, this could be the opportunity for you. Our successful Clinical Research Associates possess varied backgrounds in the medical and related healthcare fields. Individuals who have succeeded in the CRA role include Registered Nurses, Dieticians, Pharmacists, Faculty of Science Graduates and Research Assistants. An extensive training program provides the platform to carry out your duties effectively and confidently.
Please note that this role is not US based and you must be located in the country of Georgia to be considered.
Responsibilities:
- Conduct pre-study, initiation, monitoring, and closeout visits for research sites
- Perform source document verification and case report form review
- Perform regulatory document review
- Conduct study drug inventory
- Perform adverse event and serious adverse event reporting and follow-up
- Assess patient recruitment and retention
QUALIFICATIONS
- Minimum a Bachelor of science in health-related field, MD or equivalent
- Minimum of 1 year independent CRA monitoring
- Broad knowledge of medical terminology and clinical patient management
- Basic knowledge of drug therapy techniques and clinical research methodologies
- Comprehensive knowledge of Local Regulations and ICH GCP
- Excellent oral and written communication skills
- Fluency in Georgian and English
- Great attention to detail
- Must hold a valid driver’s license
- We kindly ask to submit applications in English
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.
MEDPACE PERKS:
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
AWARDS: Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, 2024 and 2025. 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:
Our European clinical activities are growing rapidly, and we are currently seeking full-time, home-based Clinical Research Associates to join our Clinical Monitoring team, in the country of Georgia.
This position will be instrumental in growing the team in Georgia and accomplishing tasks and projects that are vital to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
The Clinical Research Associate at Medpace is offered the unique opportunity to be involved at every stage of the drug development process by providing unrivalled support to our customers. If you want an exciting career where you use your medical or health background and education, travel extensively and are instrumental in the clinical trials process, this could be the opportunity for you. Our successful Clinical Research Associates possess varied backgrounds in the medical and related healthcare fields. Individuals who have succeeded in the CRA role include Registered Nurses, Dieticians, Pharmacists, Faculty of Science Graduates and Research Assistants. An extensive training program provides the platform to carry out your duties effectively and confidently.
Please note that this role is not US based and you must be located in the country of Georgia to be considered.
Responsibilities:
- Conduct pre-study, initiation, monitoring, and closeout visits for research sites
- Perform source document verification and case report form review
- Perform regulatory document review
- Conduct study drug inventory
- Perform adverse event and serious adverse event reporting and follow-up
- Assess patient recruitment and retention
QUALIFICATIONS
- Minimum a Bachelor of science in health-related field, MD or equivalent
- Minimum of 1 year independent CRA monitoring
- Broad knowledge of medical terminology and clinical patient management
- Basic knowledge of drug therapy techniques and clinical research methodologies
- Comprehensive knowledge of Local Regulations and ICH GCP
- Excellent oral and written communication skills
- Fluency in Georgian and English
- Great attention to detail
- Must hold a valid driver’s license
- We kindly ask to submit applications in English
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.
MEDPACE PERKS:
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
AWARDS: Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, 2024 and 2025. 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 60+ Clinical Research Director Jobs at Medpace
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Research Director Jobs at Medpace.
Get Access To All JobsTips for Finding Clinical Research Director Jobs at Medpace
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.
Frequently 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 visa (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.