Research Jobs at Medpace with Visa Sponsorship
Research jobs at Medpace encompass clinical development, regulatory science, and laboratory operations, with a sponsorship track record that spans multiple work visa categories. If you're an international candidate targeting a Research role here, the company has a clear history of supporting foreign national employees through the visa process.
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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 65+ Research Jobs at Medpace
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Research Jobs at Medpace.
Get Access To All JobsTips for Finding Research Jobs at Medpace
Align your credentials with GCP requirements
Medpace operates under Good Clinical Practice standards, so USCIS specialty occupation determinations for Research roles here often hinge on whether your degree and experience map directly to clinical trial protocols or regulatory submissions, not just general science.
Target therapeutic area teams strategically
Medpace organizes Research hiring around specific therapeutic areas like oncology, cardiology, and CNS. Applying to roles within your documented research focus strengthens your specialty occupation case and signals a credible fit to the hiring team.
Request OPT extension timing from your DSO early
If you're on F-1 OPT, coordinate with your Designated School Official well before your current authorization expires. Medpace's onboarding timelines can run several weeks, and a gap between your offer acceptance and OPT extension approval creates unnecessary complications.
Prepare for PERM documentation during offer negotiation
For EB-2 or EB-3 sponsorship, DOL's PERM process requires evidence that no qualified U.S. workers were available. Ask your Medpace recruiter about their standard PERM timeline upfront so you're not caught off-guard by the 12-to-18-month process window.
Use Migrate Mate to identify open Research roles
Medpace posts Research openings across multiple functions and sites. Use Migrate Mate to filter specifically for Medpace Research positions that include visa sponsorship, so you're not manually sifting through listings that won't support your immigration status.
Verify your I-94 status before starting a new position
If you're changing employers to join Medpace on an H-1B transfer, confirm your current I-94 admission period is valid and your transfer petition is filed before your last day. USCIS portability rules protect you once the new petition is received, not approved.
Frequently Asked Questions
Does Medpace sponsor H-1B visas for Research roles?
Yes, Medpace sponsors H-1B visas for Research positions, particularly in clinical research, regulatory affairs, and biostatistics. Research roles at Medpace typically qualify as specialty occupations under USCIS guidelines because they require at least a bachelor's degree in a directly related scientific or technical field. If you're already on H-1B with another employer, Medpace can file an H-1B transfer petition so you can start without waiting for cap-subject processing.
How do I apply for Research jobs at Medpace?
You can apply directly through Medpace's careers portal or find their open Research listings filtered by visa sponsorship on Migrate Mate. When applying, tailor your resume to the specific therapeutic area or functional group the role sits within, such as clinical operations, medical writing, or data management. Medpace's recruiting process typically involves a phone screen followed by one or more panel interviews with the research team.
Which visa types does Medpace commonly use for Research positions?
Medpace has sponsored H-1B, F-1 OPT, F-1 CPT, TN visa, J-1 visa, and employment-based Green Card categories including EB-2 and EB-3 for Research roles. F-1 OPT is common for recent graduates entering clinical research associate or data coordinator positions. TN visa is available for Canadian and Mexican nationals in qualifying research occupations. H-1B is the primary long-term work visa for ongoing Research employment.
What qualifications does Medpace expect for Research roles?
Most Research positions at Medpace require a bachelor's degree or higher in life sciences, pharmacy, nursing, statistics, or a directly related field, depending on the role. Clinical Research Associate and similar positions often expect prior CRA experience or therapeutic area exposure. Advanced roles in regulatory affairs or biostatistics may require a master's degree or PhD. Your degree field needs to directly align with the job function to support a specialty occupation visa petition.
How do I handle visa timing if I receive a Research offer from Medpace?
Start date coordination matters significantly at a contract research organization like Medpace. If you're on F-1 OPT, confirm your authorization end date before accepting so your employer can file an H-1B petition under cap-subject or cap-exempt rules if needed. H-1B cap-subject petitions have an October 1 start date, which may create a gap if your OPT expires mid-year. Medpace's HR team typically coordinates with outside immigration counsel, so raise your visa situation early in the offer process.