Life Science Jobs | Medpace is Hiring a Clinical Database Designer | Apply Now
Looking to grow your career in global clinical research? Medpace is hiring a Clinical Database Designer in Navi Mumbai, offering a high-impact opportunity for professionals seeking advanced life science jobs within a globally recognized CRO. This role under the Medpace career framework allows you to work on international clinical trials while strengthening your expertise in clinical research jobs and data management.
Job Details
- Job Title: Clinical Database Designer
- Location: Navi Mumbai, India
- Department: Data Management
- Job ID: 11745
About the Company
Medpace is a full-service global clinical research organization supporting Phase I–IV clinical development. The company partners with biotechnology, pharmaceutical, and medical device organizations worldwide. Medpace is known for its scientific rigor, regulatory expertise, and disciplined operational approach. With operations in over 40 countries, the organization offers international exposure. Medpace emphasizes innovation, quality, and patient-focused research. It provides structured growth pathways for long-term life science jobs.
Key Responsibilities
- Maintain eCRF and Edit Check Specification standard templates according to CDISC standards for data collection and data submission;
- Develop and maintain eCRF specifications on a study-by-study basis (e.g., reviewing protocol and customize library eCRFs to apply for the study) from database build through database lock (including Change Requests);
- Develop and maintain Edit Check Specifications from database build through database lock (including Change Requests) to ensure that all data collected are present, logical, and per expected protocol assessment schedule and completion guidelines;
- Perform validation of both the eCRF and the edits per the specifications ensuring that all possible entry scenarios are tested and documented. Accountable for providing reliable and concise feedback to clinical data programmer;
- Liaise and educate the Data Manager and Sponsor to ensure that eCRFs are well understood, and the EDC database is set up per Sponsor expectations (e.g., attend ongoing meetings with the Sponsor during setup of study);
- Liaise with Clinical Db Programmer to ensure that eCRF and Edit Check Specifications are clearly defined and can be accomplished in the referenced system;
- Design and develop customized project-level reports that are useful to the team via the reporting tools within the EDC systems (e.g., Business Objects, JReview);
- Lead eCRF specification review meetings with internal project team to discuss eCRF specifications; and
- Lead eCRF specification review meetings with external project team to discuss eCRF specifications and speak knowledgeably about decisions made and technical design options if Sponsor does not agree with current design.
Qualifications
Bachelor’s degree/Advanced degree in Life Sciences or equivalent
Skills
- At least one year experience building specifications and/or performing UAT for EDC databases
- Excellent verbal and written communication skills
- Meticulous attention to detail.
The Clinical Database Designer role at Medpace is a valuable opportunity for professionals seeking meaningful clinical research jobs with global exposure. With structured career paths, strong mentorship, and advanced clinical projects, this position stands out among life science jobs for candidates looking to grow within a trusted Medpace career environment.
