Clinical Database Programmer-EDC

Johnson & Johnson

Closes in 2 days Remote

Quick summary

Work type
Remote
Location
Warsaw, INRaynham, MAWest Chester, PA
Salary
$109,000–$174,800 / yr
Posted
6 days ago
Closes
Jun 18, 2026 (soon)

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $163k
This role $142k
$98k most similar roles pay here $216k

This role pays less than 66% of similar roles. Most pay $126,800–$198,800 — the shaded band above. At the midpoint, this role pays about $142k versus about $163k for comparable roles.

Based on 240 similar postings.

Employer

About Johnson & Johnson

Johnson & Johnson is a multinational corporation operating in three main segments: consumer health products, pharmaceuticals, and medical devices, known for brands like Tylenol, Band-Aid, and Janssen. Industry: Pharmaceuticals & Medical Devices

Johnson & Johnson currently has 63 open roles on FindRole.

Listed pay typically runs $117,000–$201,250 across 61 roles with salary data.

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View all roles at Johnson & Johnson

At a glance

TL;DR · Clinical Database Programmer-EDC

Join our DePuy Synthes team as a Lead Clinical Database Programmer with EDC in Warsaw, IN; Raynham, MA; or West Chester, PA. This senior-level position involves coordinating timelines and resources for clinical systems implementation and maintenance, collaborating with Data Management leadership to define data standards, and providing oversight of study-specific system set-ups across platforms like CTMS, eTMF, IxRS, and EDC. You will support vendor evaluations, develop project management plans, mentor peers, and ensure compliance with GCP and SDLC. The ideal candidate has a Bachelor’s degree in Statistics or Computer Science, at least 6 years of clinical research experience, proficiency in Medidata or Veeva systems, and knowledge of CDISC STDM. Strong communication skills and familiarity with Clinical Operations are preferred.

What you'll do

  • Define and document data and process standards with Data Management leadership.
  • Develop project management plans for trial execution including timelines and milestones.
  • Lead the deployment of EDC Systems, CTMS, eTMF, IxRS, and other relevant platforms.
  • Facilitate quality review processes by mentoring peers to minimize delays.
  • Serve as first line of contact from study initiation through go live for clinical systems.

What we're looking for

  • Bachelor’s degree in Statistics, Computer Science or related field with 6+ years of clinical research experience.
  • Proven experience managing projects and delivering critical milestones in a team environment.
  • Strong proficiency in Medidata or Veeva systems; advanced certification preferred.
  • Experience with at least one clinical system (EDC, CTMS, eTMF, IxRS); strong proficiency in multiple systems preferred.
  • Excellent verbal and written communication skills required.
  • Knowledge of GCP and SDLC preferred; CDISC STDM experience beneficial.

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