Medpace Hiring Clinical Database Programmer

Clinical Database Programmer | Life Sciences | Mumbai
Medpace hiring Clinical Database Programmer in Mumbai. Life Sciences grads, Pharma/CRO experience preferred. Apply now for growth opportunities.
URL Slug: medpace-clinical-database-programmer

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Join Medpace as a Clinical Database Programmer in Mumbai and be part of a global CRO driving innovation in clinical research. This role offers hands-on experience in programming, validation, and data management for critical clinical trials. If you are detail-oriented, skilled in Rave or Veeva EDC, and want to advance your career in Pharma/CRO, this position is designed for you.

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Company Overview

Medpace is a full-service global clinical contract research organization (CRO) providing Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries. With over 30 years of experience, Medpace is committed to accelerating the development of safe and effective medical therapeutics through scientific and disciplined approaches.

Key Highlights:

• Headquartered in Cincinnati, Ohio, with over 5,000 employees across 40+ countries

• Expertise across major therapeutic areas: oncology, cardiology, metabolic disease, CNS, anti-viral, anti-infective

• Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021-2024)

• Recipient of CRO Leadership Awards from Life Science Leader magazine

Medpace values people, purpose, and passion, fostering an inclusive environment where employees contribute to advancing patient health globally.

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Job Role & Responsibilities

As a Clinical Database Programmer, you will work closely with the Biometrics and Data Management teams to ensure accurate, high-quality clinical trial databases that meet regulatory and company standards.

Key Responsibilities:

• Develop, program, validate, and maintain clinical trial databases

• Maintain and enhance the company library of CDASH-compliant CRFs

• Serve as the primary technical contact for assigned studies with the Data Management team

• Ensure adherence to company standards and quality expectations in all programming tasks

• Troubleshoot and resolve database issues efficiently

• Support clinical operations and cross-functional teams to meet study timelines

Technical Requirements:

• Strong proficiency in Medidata Rave study build or Veeva EDC systems

• Experience with custom functions using C# programming is preferred

• Certified Medidata Rave Study Builder certification is a plus

• Meticulous attention to detail to ensure database integrity and compliance

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Eligibility / Qualifications

Educational Requirements:

• Bachelor’s or Advanced Degree in Life Sciences, Computer Science, or related field

• Courses: B.Sc. (Biology, Biotechnology, Microbiology), B.Tech (Bioinformatics), M.Sc. (Life Sciences, Biostatistics), BCA, MCA

Experience Requirements:

• Prior experience in clinical database programming in Pharma, Biotech, or CRO environment

• Hands-on experience with Rave or Veeva EDC systems

• Knowledge of CDASH standards and clinical data management processes

Skills & Competencies:

• Strong verbal and written communication skills

• Excellent analytical, problem-solving, and organizational skills

• Ability to work independently and collaboratively in a fast-paced clinical research environment

• Familiarity with regulatory compliance requirements for clinical data

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Location & Work Setup

Location: Navi Mumbai, Maharashtra, India
Work Type: Full-time, office-based

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Why Medpace?

Joining Medpace offers more than a job – it’s a chance to grow professionally while contributing to life-saving research.

Perks and Benefits:

• Flexible work environment and competitive compensation

• Structured career paths with professional development opportunities

• PTO packages, health and wellness initiatives, and employee appreciation programs

• Recognition through awards and professional achievements

• Exposure to global clinical research projects across multiple therapeutic areas

Career Growth: Medpace encourages learning and skill development, ensuring employees stay at the forefront of clinical research innovations.

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Application Process

To apply for the Clinical Database Programmer role at Medpace:

1. Submit your updated resume highlighting relevant clinical database programming experience

2. Wait for a review by a Medpace team member; shortlisted candidates will be contacted for next steps

3. Prepare for technical assessments focusing on Rave/Veeva EDC systems, CDASH compliance, and programming skills

CTA Optimization: Apply today to join a globally recognized CRO and accelerate your career in clinical research! Opportunities are limited – secure your spot now.

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FAQs

Q1. What are the eligibility criteria for this role?
A1. Bachelor’s or Advanced Degree in Life Sciences or Computer Science with relevant clinical database programming experience.

Q2. Is Medidata Rave or Veeva experience mandatory?
A2. Yes, experience in Rave study build or Veeva EDC is highly preferred for this position.

Q3. Can fresh graduates apply?
A3. This position requires prior experience; fresh graduates may explore entry-level roles at Medpace.

Q4. Where is the job located?
A4. Navi Mumbai, Maharashtra, India – full-time, office-based.

Q5. What skills are essential for success?
A5. Strong programming skills, attention to detail, familiarity with CDASH-compliant CRFs, analytical thinking, and excellent communication.

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Medpace Clinical Database Programmer – Summary Table