Clinical Study Builder | India | Permanent
Location: Remote, India
Employment Type: Full-Time, Permanent
Industry: Clinical Research / CRO
Company: Indero (Formerly Innovaderm)
About the Role
Indero is seeking a skilled Clinical Study Builder to join our global clinical research team. In this role, you will collaborate closely with data management and statistical teams to design, develop, and implement electronic case report forms (eCRFs), visit schedules, and data quality checks for clinical research studies. You will primarily work on Medidata Rave CDMS, with potential exposure to Medrio and Veeva EDC systems.
As a Clinical Study Builder, you will ensure that all study builds are aligned with regulatory requirements, industry guidelines, and company SOPs while meeting sponsor expectations and timelines. This is a home-based position in India, with occasional meetings outside standard business hours.
Key Responsibilities
Develop and configure eCRFs, folders, edit checks, derivations, integrations, migrations, and reports per protocol specifications.
Set up Coder, Local Lab, and Targeted SDV modules in Rave CDMS.
Lead eCRF design and review meetings, providing guidance on best practices.
Provide technical support and user training for study teams.
Collaborate with Lead Data Managers and vendor partners to ensure smooth testing and deployment of study builds.
Troubleshoot and resolve technical issues promptly.
Participate in writing and updating Rave CDMS SOPs.
Ensure compliance with Good Clinical Practices (GCP), ICH guidelines, and other applicable regulatory standards.
Required Qualifications & Experience
Education: B.Sc. or M.Sc. in Life Sciences, Pharmacy, Biotechnology, or related fields.
Experience: 2–4 years of hands-on experience in Rave CDMS study build.
Skills:
Certified Rave Study Builder preferred.
Practical experience with Medidata Rave, Medrio, or Veeva EDC.
Strong understanding of case report form design, database programming, and clinical trial workflows.
Ability to lead multiple study builds or post-release changes simultaneously.
Highly organized with excellent project management and time management skills.
Strong verbal and written communication in English.
Knowledge of drug development processes, regulations, and standards in clinical research.
About Indero
Indero (formerly Innovaderm) is a global clinical research leader in dermatology and rheumatology. With over 25 years of experience, we provide end-to-end clinical trial services including protocol design, patient recruitment, trial monitoring, and biometrics. Our dual-focus CRO model ensures specialized expertise while maintaining global reach across North America, Europe, Asia Pacific, and Latin America.
Why Join Us:
Work in a collaborative, innovative, and responsive environment.
Flexible work schedule and remote work from India.
Opportunities for professional development and skill growth.
Exposure to global clinical trial standards and cutting-edge CRO operations.
Location: Home-based, India (attendance at occasional evening meetings required)
Work Authorization: Must be legally eligible to work in India
Equal Opportunity Employer: Indero is committed to diversity, equity, and providing accommodations for candidates with disabilities.
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Netherlands |Remote Australia :
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Sheffield |Oxfordshire :
Witney |Ontario :
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Japan | Saitama |Tokyo :
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