Clinical Database Programmer (Mumbai)

Medpace, Inc.; Navi Mumbai; On-site; INR 900,000 - 1,500,000; Full time

Benefits offered by this job

Health & retirement benefits

PTO & wellness

Office-based with occasional WFH

Company events

Job summary

Medpace, Inc. in Navi Mumbai is seeking a full-time Clinical Database Programmer to join our Biometrics team.

You will develop, validate, and maintain clinical trial databases, support CDASH CRFs, and act as primary data-management contact for studies. Ideal candidates have a Life Sciences or CS degree, experience in Medidata Rave and Veeva EDC, strong C# programming, and excellent communication with meticulous attention to detail.

Qualifications

• Bachelor’s degree/Advanced degree in Life Sciences or Computer Science or equivalent.
• Rave study build and/or Veeva EDC experience in a similar position in Pharma/Healthcare sector preferred.
• Custom function (C# Programming) experience is preferred.
• Certified Medidata Rave Study Builders preferred.
• Excellent verbal and written communication skills; and
• Meticulous attention to detail.

Responsibilities

• Develop, program, validate and maintain clinical trial databases according to company standards;
• Maintain and contribute to company library of standard CDASH compliant CRFs; and
• Act as primary contact to the data management team for assigned studies, supplying all necessary technical support, and ensuring quality of the programming and adherence to company standards.

Skills

Verbal and written communication

Attention to detail

Education

Bachelor’s degree/Advanced degree in Life Sciences or Computer Science or equivalent

Tools

C# Programming

Medidata Rave

Veeva EDC

Job description

Job Summary

Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Database Programmer to join our Biometrics team. This position will work in a team to accomplish tasks and projects that are instrumental 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.

Responsibilities

• Develop, program, validate and maintain clinical trial databases according to company standards;
• Maintain and contribute to company library of standard CDASH compliant CRFs; and
• Act as primary contact to the data management team for assigned studies, supplying all necessary technical support, and ensuring quality of the programming and adherence to company standards.

Qualifications

• Bachelor’s degree/Advanced degree in Life Sciences or Computer Science or equivalent;
• Rave study build and/or Veeva EDC experience in a similar position in Pharma/Healthcare sector preferred;
• Custom function (C# Programming) experience is preferred;
• Certified Medidata Rave Study Builders preferred;
• Excellent verbal and written communication skills; and
• Meticulous attention to detail.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
  • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• • Office based environment with on-site mentors
  • Defined career paths with clear advancement opportunities
  • Industry renowned onboarding and training programs designed to accelerate professional development
  • Ongoing training and continuous learning opportunities throughout your career
  • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• • Competitive compensation programs that recognize and reward performance
  • Comprehensive health, wellness, retirement, and PTO benefits
  • Office based culture with occasional WFH that provides flexibility for eligible positions after training
  • Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.