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Senior EDC Lead

Job in Camden, Camden County, New Jersey, 08100, USA
Listing for: AbbVie
Full Time position
Listed on 2026-06-18
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

About Abb Vie

Abb Vie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience, and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit  Follow @abbvie on Linked In, Facebook, Instagram, X and You Tube.

Purpose

Abb Vie Data Science is the best-in‑class team within its cross‑industry peer group and is responsible for bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and innovation. This role is key to ensuring successful delivery against the program‑ and study‑level accountabilities assigned to Clinical Data Strategy Organization.

Responsibilities
  • Actively participates in the development of common data standards and ensures systems designs comply with the standards, as well as with associated protocol requirements. Ensures that the design team utilizes standards.
  • Establishes and maintains methodology used by the team to design and develop clinical trial systems, benchmarking against industry standards. Ensures that systems are specified to optimize on functionality, end user experience, and data flow. Ensures that the design team meets these expectations.
  • Ensures that TA‑ and program‑level consistency is achieved by the design team.
  • Accountable for the on‑time design and delivery of new clinical systems, integrations between systems, as well as any required changes to clinical systems (e.g., EDC, IRT, ePRO). Utilizes project management tools to track study progress and plan work. Anticipates and identifies issues that could affect timelines or quality and develops options and solutions.
  • Interacts with and influences CDO and cross‑functional team members to achieve program and study objectives. Ensures that assigned work product is synchronized with upstream and downstream dependencies.
  • Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs), and to functional quality standards. Stays abreast of new and/or evolving local regulations, guidelines and policies related to clinical development.
  • Responsible for coaching and mentoring members of the team, as well as contributes to their skill development.
  • Leads CDO and cross‑functional innovation and process improvement initiatives.
Qualifications
  • Bachelor’s degree in business, management information systems, computer science, life sciences or equivalent. Master’s preferred.
  • Must have 5+ years of hands‑on technical Study build in EDC. Experience with technical study build in Medidata RAVE is required. Veeva EDC technical study build experience is a plus.
  • In‑depth knowledge of clinical trial process.
  • In‑depth knowledge of CDASH (Required) and SDTM.
  • Demonstrated performance as a key contributor to initiatives and advancement of the organization.
  • Demonstrated ability to influence others without direct authority; demonstrated ability to successfully coach/mentor in a matrixed environment; demonstrated effective communication skills and analytical skills.
Compensation and Benefits
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range.

    This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short‑term incentive programs.

Note:

No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employer remains in the Company’s sole and absolute discretion until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

Abb Vie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit

US & Puerto Rico applicants seeking a reasonable accommodation,  to learn more:

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Position Requirements
10+ Years work experience
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