Manager, EDC Database Programming

Initial Therapeutics, Inc.; Basking Ridge (NJ); On-site; USD 127,280 - 190,920; Full time

Job summary

Initial Therapeutics, Inc. is seeking a Manager of EDC Database Programming. This role requires oversight of electronic data capture systems for clinical studies, ensuring high-quality builds and adherence to specifications.

The ideal candidate will have a background in Life Sciences, with at least 5 years of experience in EDC study build and database programming. A master’s degree is preferred. The position involves collaboration with CROs and service providers to deliver high-quality outcomes.

Qualifications

• Minimum of 5 years of EDC study build and database programming experience in the pharmaceutical or CRO industry.
• Strong background in clinical programming and project management.
• Ability to work collaboratively at different levels and manage multiple priorities.

Responsibilities

• Manage study build activities ensuring quality and adherence to specifications.
• Collaborate with CROs and service providers for timely and high-quality study builds.
• Lead functional and user acceptance testing, including edit check and custom function programming.

Skills

EDC study build experience

Clinical Programming expertise

Data validation programming

Communication skills

Project Management

Education

Bachelor's Degree in Life Sciences

Master's Degree

Tools

CTMS

EDC

Clinical Data Repository

CDASH & CDISC standards

Job description

Job Title: Manager, EDC Database Programming

Job Requisition ID: 1733

Posting Start Date: 7/2/26

Job Summary

The Manager, EDC Database Programming is a member of the Biostatistics and Data Management team and serves as a subject matter expert for the oversight, guidance, and design of study build activities for all clinical studies Electronic Data Capture systems and other related technologies, Clinical Data Programming and Reporting. The scope of work includes ownership and oversight of the study design, build, edit check and custom function programming activities, including the review of CRF specifications and data validation specifications. In addition, the position involves assisting with functional and user acceptance testing, and managing quality deliverables in partnership with RAVE Administrator, Study Data Managers, and functional service providers. The individual will also engage in the governance, management, and advancement of DS Global Library Standards. This position will work closely with other members of the Biostatistics and Data Management, external CRO partners, service providers, and other stakeholders.

Responsibilities

• Provide guidance and manage accountability for the study build activities ensuring high quality, consistency, and adherence to eCRF specifications established for each study.
• Manage all study build deliverables for the timely delivery and implementation of high-quality study builds for all studies in conformance with DS standards and eCRF specifications.
• Manage and maintain administrative, operational deliverables, and timelines pertaining to study build activities, edit check programming, and custom function development, including proactive review, testing, and supporting documentation.
• Collaborate with the study data managers, external CROs, and service providers to ensure study build configuration is reviewed, tested, and completed with high quality in a timely manner.
• Guide the operational execution of the steps and procedures for consistency and accuracy pertaining to the delivery of high-quality study builds for all studies.
• Proactively identify and resolve issues that may influence and/or impact study build quality and other deliverables.
• Serve as a subject matter expert and provide oversight, guidance, and design of study build activities for all studies.
• Establish and confirm design specifications of study build activities including core configuration, eCRFs, Data Validation Specifications (DVS), and Reporting.
• Establish and confirm the configuration of the EDC study build in conformance with study design specifications for eCRFs, DVS, Custom Functions, tSDV, RAVE Safety Gateway, Integrations, and Reporting.
• Establish and implement edit check and custom functions programming standards.
• Review and provide input to quality database designs for fit and feasibility within the EDC application and ensure consistency with established standards.
• Ensure that the system interfaces are designed and configured for optimal use and not in conflict with the study build and relevant specifications.
• Lead and/or provide oversight to functional and user acceptance testing activities including edit check and custom function test scripts, programming, and validation tasks; ensure CRF screens for the study conforms to the CRF specifications and configuration.
• Lead and/or provide oversight on the impact analysis and risk assessment of study build change requests, maintain documentation, and facilitate the implementation of changes as per the change control procedures.
• Track, debug, and resolve issues pertaining to study build and programming tasks for all studies.
• Identify opportunities for continuous process improvements, improve work procedures, QC procedures, checklists to track milestones, status, and issues; ensure traceability, and study build performance metrics.
• Contribute to the development of content and training pertaining to all aspects of the study build activities in partnership with the study data managers and the functional service provider(s).

Qualifications

Education Qualifications — Bachelor's Degree in Life Sciences or related field required; Master's Degree preferred.

• Minimum of 5 years of EDC study build and database programming experience and data validation programming in the device/pharmaceutical/CRO industry (Required).
• Expertise in Clinical Programming, methods, and techniques (Required).
• Knowledge of industry standard clinical technologies including CTMS, EDC, Clinical Data Repository (CDR); knowledge of CDASH and CDISC data standards; knowledge and understanding of data acquisition and integration tools and technologies (Required).
• Work collaboratively with people at different levels of experience, different disciplines, and cultures.
• Self‑directed; able to work independently.
• Strong communication, negotiation, and conflict resolution skills.
• Ability to manage multiple priorities.
• Strong background in Clinical Programming, Project Management, and data acquisition methods.

Salary Range

USD$127,280.00 - USD$190,920.00

Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.