Navi Mumbai, Maharashtra, India · On-site
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Software Engineer to join our Information Technology team. The Software Engineer position will work on Administrative S…
Skills: C#, SQL, ASP.NET, Angular, Webservices
Navi Mumbai, Maharashtra, India · On-site
Our corporate activities are growing rapidly, and we are currently seeking a full-time Software Testing Manager to join our Information Technology team in Mumbai. This position will manage a team of software testing engi…
Skills: Software Testing Management, SDLC, Validation Planning, User Acceptance Testing, Traceability Matrices
Cincinnati, Ohio, United States · On-site
Candidates with a PhD in Statistics or Biostatistics - join us virtually on Wednesday, July 15th to learn about our Biostatistician role here at Medpace, based in Cincinnati. Medpace will be hosting a Virtual Hiring Even…
Skills: SAS Programming, Statistical Methodology, Clinical Development Planning, Study Protocol Review, Data Analysis
Cincinnati, Ohio, United States · On-site
Medpace is a rapidly growing global full-service Contract Research Organization with our global headquarters in Cincinnati, OH and operations in more than 40 countries. As we continue to expand our recruitment efforts, w…
Skills: Background Check Processing, Interview Scheduling, Recruitment Assistance, Document Management, Microsoft Word
City of London, England, United Kingdom · On-site
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Contract Specialist to join our Clinical Operations team. This position plays a key role in the study start-u…
Skills: Contract Negotiation, Budget Negotiation, Clinical Trial Management, Administrative Support, Communication Skills
Seoul, South Korea · On-site
We are currently seeking a full-time, office based Regulatory (Study Start up) Submissions Coordinator to join our Clinical Operations team in the Seoul office. This role is a vital part of the team to accomplish tasks a…
Skills: Regulatory Submissions, Clinical Trial Activation, English Communication, Microsoft Office, ICH-GCP Guidelines
Munich, Bavaria, Germany · On-site
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time office-based Regulatory Submissions Coordinator to join our Clinical Operations team in Munich. This position plays a key r…
Skills: Regulatory Submissions, Clinical Trial Management, Document Collection, Compliance Monitoring, German Language Proficiency
Cincinnati, Ohio, United States · On-site
The Laboratory Technologist at Medpace Reference Laboratories plays a pivotal role in research based drug development within the pharmaceutical industry. Due to our recent growth, we are in need of qualified and focused …
Skills: Clinical laboratory testing, Standard Operating Procedures (SOPs), Laboratory information system, Quality control, Preventative maintenance
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The role involves designing, developing, and supporting software applications for administrative systems and modernizing aging applications. Responsibilities include gathering user requirements, executing test plans, and following the full software development life cycle.
Candidates must have a Bachelor's degree in Computer Science and at least 2 years of experience with C#, Angular, and relational databases. Proficiency in Azure, Entity Framework, and SDLC is highly desired.
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Software Engineer to join our Information Technology team. The Software Engineer position will work on Administrative Systems and modernization of aging applications. Strong attention to detail, desire for process ownership, and interest in implementing new technology are highly valued.
This is an incredible opportunity to join, contribute, and shape a new team, while also being a part of a large, fast-growing organization. You will be joining an organization where your contribution makes a significant impact in positively impacting people's lives, as new treatments and therapeutics are developed.
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.
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
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What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Accelerating Drug, Biologic and Medical Device Clinical Development
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 6,300 people across 46 countries.
Offices: 5375 Medpace Way, Cincinnati, OH 45227, US
Accelerating Drug, Biologic and Medical Device Clinical Development
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 6,300 people across 46 countries.
Offices: 5375 Medpace Way, Cincinnati, OH 45227, US
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