Medpace is growing rapidly, and we are currently seeking a full-time, office-based SDET to join our Information Technology (IT) team in our Mumbai office. The SDET position is a vital role whose success relies upon your knowledge, experience, and dedication. The Medpace IT department delivers software solutions that enable and empower both internal and external customers to manage their business processes most effectively and efficiently. Our SDETs ensure these custom solutions are designed, built, and implemented correctly.
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 5,000 people across almost 40 countries.
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work weve 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.
Keyskills: python software development analytical languages time management automation testing custom interpersonal skills javascript cypress java automation selenium application white box testing sdet regression software solutions api web application testing programming
Medpace’s dedicated teams serve as an extension of your team – we engage quickly and provide strategic thinking – ensuring start-up times are met, superior quality, and the most efficient delivery of every phase of your clinical trial. Our therapeutic and regulatory experts are ...