M

Medpace

Global CRO delivering full-service clinical trials

Clinical Application IT Support

IT Service Desk & End User SupportConfirmed live in the last 24 hours
Full-timeNavi Mumbai, Maharashtra, IndiaNo salary listed

About the Job

Requirements

  • A bachelor's degree in Information Technology, Computer Science, Biomedical Engineering, Life Sciences, or a related field, or equivalent experience.
  • One to three years of application or technical support experience; experience in a CRO, pharmaceutical, or clinical research environment is preferred.
  • Strong analytical and problem-solving abilities.
  • Excellent communication skills and the ability to work cross-functionally with staff, vendors, and external users from multiple countries.
  • Good organizational skills, attention to detail, and flexibility.
  • Ability to work concurrently on several issues and projects, each with specific requirements.
  • Competence in software installation and troubleshooting.
  • Demonstrated ability to learn new technologies and applications.
  • Knowledge of Microsoft Windows operating systems.

Responsibilities

  • Provide technical support for clinical research and core lab platforms, including medical imaging, ECG, connected medical devices, mobile applications, and virtualized workstations.
  • Deliver customer service to internal users, central readers, and investigator sites located globally.
  • Troubleshoot and resolve technical and workflow issues, escalating to appropriate teams when needed.
  • Log, track, and document incidents and service requests through resolution using the ticketing system.
  • Perform software installation, configuration, testing, and validation in accordance with company procedures.
  • Act as a liaison between end users, internal development teams, core infrastructure teams, and external vendors while maintaining the interests of end users.
  • Coordinate escalations and follow up with stakeholders to ensure seamless operations across clinical trials.
  • Create and maintain support documentation, knowledge base articles, and user guides.
  • Ensure support activities comply with applicable regulatory standards, including GCP, 21 CFR Part 11, and HIPAA/GDPR.
  • Perform other system-related tasks to meet company objectives.

Desired Qualifications

  • Hands-on familiarity with virtualized environments, mobile/device support, and ticketing systems.
  • Understanding of regulatory standards such as GCP, 21 CFR Part 11, and HIPAA/GDPR.
  • Experience in a CRO, pharmaceutical, or clinical research environment.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

Recently Posted Jobs

Explore more opportunities at Medpace

See more jobs