Clinical Research Associate Jobs at Medpace with Visa Sponsorship
Clinical Research Associate jobs at Medpace support clinical trials across therapeutic areas including oncology, cardiology, and metabolic disease. The company has a track record of sponsoring work visas for this function, making it a realistic target if you need sponsorship to work in the U.S.
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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 Clinical Research Associate Jobs at Medpace
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Research Associate Jobs at Medpace.
Get Access To All JobsTips for Finding Clinical Research Associate Jobs at Medpace
Align Your Credentials to GCP Standards
Medpace expects CRAs to demonstrate ICH E6 Good Clinical Practice training and hands-on monitoring experience before an offer stage. Certifying through ACRP or SOCRA before you apply signals you can step into site visits without a ramp-up period.
Target Therapeutic Areas Medpace Actively Monitors
Medpace runs a high volume of oncology, metabolic disease, and cardiovascular trials. Framing your resume around monitoring experience in those specific areas makes your application directly relevant rather than generically clinical research.
Clarify Your OPT or Grace Period Timeline Early
If you're on F-1 OPT, confirm your authorization end date before your first interview. Medpace's HR team needs enough runway to file an H-1B cap-subject petition or request a timely cap-exempt filing if you qualify, so surface your timeline in the recruiter screen.
Understand How Medpace Structures Sponsorship Offers
Medpace typically sponsors through the standard H-1B cap process, which means a new petition filed in April with an October 1 start date. If you're interviewing in late spring or summer, discuss bridge options with HR so there's no gap in your work authorization.
Use Migrate Mate to Identify Open CRA Roles
Filtering for Clinical Research Associate openings that explicitly include visa sponsorship saves time you'd otherwise spend cold-emailing recruiters. Migrate Mate lets you search Medpace CRA listings confirmed for sponsorship, so you apply where your visa situation is already a known fit.
Prepare Your LCA Documentation Before the Offer
Your employer files the Labor Condition Application with DOL before USCIS can adjudicate your H-1B petition. Ask Medpace's immigration team early in the process whether they use internal counsel or outside firms, so you're ready to supply degree certificates and transcripts without delays.
Frequently Asked Questions
Does Medpace sponsor H-1B visas for Clinical Research Associates?
Yes, Medpace sponsors H-1B visas for Clinical Research Associates. The company has a consistent track record of filing petitions for this role, which qualifies as a specialty occupation under USCIS criteria given its degree requirements in life sciences or a related field. Cap-subject filings follow the standard April lottery cycle with an October 1 start date.
Which visa types does Medpace commonly use for Clinical Research Associate roles?
Medpace uses H-1B as the primary long-term work visa for CRAs. F-1 OPT and CPT are accepted during the pre-H-1B phase, and J-1 visa exchange visitor status can apply to qualifying candidates. TN visa classification is available for Canadian and Mexican nationals whose CRA role meets the USMCA scientist or technologist category. Green Card sponsorship through EB-2 or EB-3 is also part of the pathway for longer-tenured employees.
What qualifications does Medpace expect for Clinical Research Associate positions?
Medpace generally looks for a bachelor's degree in a life sciences field such as biology, nursing, or pharmacy, paired with prior clinical monitoring or site coordination experience. ICH E6 GCP certification is expected, and therapeutic area experience in oncology, cardiology, or metabolic disease is a strong differentiator. Remote and on-site monitoring competence both matter given Medpace's hybrid trial management model.
How do I apply for Clinical Research Associate jobs at Medpace?
You can browse current Clinical Research Associate openings at Medpace through Migrate Mate, which filters for roles that include visa sponsorship so you know upfront whether your immigration situation is supported. From there, applications typically go through Medpace's own careers portal. Tailoring your application to the specific therapeutic area listed in the job description noticeably improves response rates from their recruiting team.
How do I time my H-1B filing if I receive a Medpace offer while on OPT?
If your OPT is still valid when Medpace extends an offer, the company can file your H-1B petition during the April registration window. USCIS's cap-gap rule then automatically extends your F-1 OPT work authorization through September 30 if your OPT would otherwise expire before your H-1B start date. Communicate your OPT expiration date to Medpace's HR team as early as the offer conversation to ensure the filing timeline works.