Research Specialist Jobs at Medpace with Visa Sponsorship
Research Specialist jobs at Medpace support clinical trial operations across a range of therapeutic areas. The company has a consistent track record of sponsoring work visas for this function, making it a realistic target if you're on OPT, H-1B visa, or pursuing longer-term permanent residency pathways.
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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 Specialist Jobs at Medpace
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Research Specialist Jobs at Medpace.
Get Access To All JobsTips for Finding Research Specialist Jobs at Medpace
Align Your Degree to Clinical Research Directly
Medpace Research Specialist roles typically require a life sciences or health-related degree. Before applying, confirm your transcripts show coursework in biology, pharmacology, or a related field, since USCIS scrutinizes specialty occupation ties closely for CRO roles.
Target Therapeutic Areas Medpace Actively Staffs
Medpace concentrates heavily in oncology, cardiovascular, and metabolic disease studies. Positioning your research background within these areas in your resume makes your application more relevant to the teams that have active hiring cycles and open requisitions.
Request Sponsorship Confirmation Before Final Interviews
Medpace sponsors across multiple visa categories, but not every hiring manager controls that decision. Ask your recruiter explicitly which visa types are supported for the specific Research Specialist role before you reach the offer stage to avoid late-stage delays.
Use Migrate Mate to Filter Verified Sponsorship Openings
Search Migrate Mate to browse Research Specialist positions at Medpace that have confirmed sponsorship history. Filtering by visa type lets you prioritize roles where your specific status, whether F-1 OPT, H-1B, or TN, has precedent at this employer.
Plan OPT Timing Around Medpace Hiring Cycles
F-1 graduates have a 60-day grace period after program completion before OPT authorization kicks in. If your graduation date falls mid-quarter, coordinate your application timeline so your OPT start date aligns with Medpace onboarding windows, which tend to follow study startup schedules.
Prepare for PERM Labor Market Evidence Early
If your goal is an EB-2 or EB-3 Green Card through Medpace, the DOL PERM process requires the employer to document that no qualified U.S. worker was available. Understanding this before you accept an offer helps you set realistic multi-year sponsorship expectations with your hiring team.
Frequently Asked Questions
Does Medpace sponsor H-1B visas for Research Specialists?
Yes, Medpace sponsors H-1B visas for Research Specialist roles. The position typically qualifies as a specialty occupation given the degree requirements tied to clinical research work. Because H-1B approval depends on USCIS review of the specific role and your credentials, you should confirm sponsorship intent with your recruiter early in the process rather than assuming it after an offer is extended.
How do I apply for Research Specialist jobs at Medpace?
Applications go through Medpace's careers portal, where Research Specialist openings are listed by therapeutic area and site location. You can also browse verified sponsorship-eligible openings on Migrate Mate, which filters Medpace roles by visa type so you can identify positions where your specific immigration status has sponsorship precedent before you invest time in applying.
Which visa types does Medpace commonly use for Research Specialist roles?
Medpace supports several visa categories for Research Specialists, including H-1B, F-1 OPT and CPT, TN visa for Canadian and Mexican nationals, J-1 visa for exchange visitors, and EB-2 or EB-3 Green Card pathways for longer-term sponsorship. The right category depends on your nationality, degree level, and where you are in your career. TN visa is available immediately for qualifying Canadian and Mexican nationals without a lottery requirement.
What qualifications does Medpace expect for Research Specialist positions?
Most Research Specialist roles at Medpace require a bachelor's degree in a life sciences field such as biology, chemistry, nursing, or pharmacology. Some positions, particularly those focused on data or regulatory work, may prefer a master's degree. Prior clinical trial experience or familiarity with Good Clinical Practice guidelines strengthens an application significantly. For visa purposes, your degree must align specifically with the duties of the role to satisfy USCIS specialty occupation standards.
How long does the visa sponsorship process take when joining Medpace as a Research Specialist?
Timeline depends on your visa category. F-1 OPT authorization from USCIS can take up to 90 days, so apply well before your program ends. H-1B standard processing runs three to six months, while premium processing brings that down to roughly 15 business days for an additional fee. Green Card sponsorship through PERM is a multi-year process. Aligning your start date expectations with your recruiter before signing an offer avoids onboarding conflicts.