EDC Developer / Programmer

Celerion

Phoenix (AZ)

Remote

USD 80,000 - 100,000

Full time

14 days+

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Job summary

A leading clinical research organization is seeking a full-time Electronic Data Capture (EDC) Database Developer. You will design and administer EDC trials, ensuring high-quality data management. Ideal candidates have a Bachelor's degree and at least 3 years of clinical data management experience, with proficiency in SQL and EDC systems. This remote position allows for periodic travel for meetings and training.

Qualifications

  • 3 years of clinical data management experience required.
  • Ability to develop SQL programming for projects.
  • Experience with EDC systems preferred.

Responsibilities

  • Serve as a subject matter expert in Veeva Clinical Data Management Suite.
  • Perform eCRF design and EDC build programming.
  • Ensure secure database imports from vendor transfers.

Skills

SQL programming
EDC systems experience
Clinical data management
Communication
Organizational skills

Education

Bachelor’s degree in a related field

Tools

Veeva CDMS
Medidata RAVE

Job description

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Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!

We are looking for a performance-oriented, innovative and self-motivated team player to join our Clinical Data Sciences team as a full-time Electronic Data Capture (EDC) Database Developer / Clinical Programmer. You will be responsible for administration of EDC Database including evaluation, analysis, design and/ or recommendations to achieve goals and excellent results in a fast-paced, ever-changing environment.

This is a full time, remote opportunity, but may travel for training and key meetings.

As an EDC Database Developer, you will build and administer EDC trials for client contracted projects including protocol/requirements evaluation, electronic case report form (eCRF) design and build with corresponding edits. This role will have technical interaction with vendors that are supporting the applications and troubleshoot/ escalate problems on systems to appropriate partners. This role will provide expert guidance to the design, development, validation, implementation and maintenance of study set-up. Additionally, this role will manage the deployment of EDC trials and set up interface connections between EDC and other systems.

Responsibilities
  • Serve as a subject matter expert in Veeva Clinical Data Management Suite (CDMS), including Veeva Electronic Data Capture (EDC) and Veeva Clinical Database (CDB)
  • Perform all activities related to eCRF design and EDC build programming for assigned projects
  • Perform EDC edit check programming for assigned projects based on edit check specifications for both simple and complex edit checks
  • Create test data to verify both screen design and edit check programming prior to deploying to User Acceptance Testing (UAT)
  • Set up test environments and coordinate project team members for execution of test scripts
  • Program and configure listings and reports using clinical reporting tools such as Veeva Clinical Database (CDB)
  • Ensure secure and high-integrity database imports from vendor transfers using Celerion data transfer standards
  • Assist with the validation of upgrades to hardware/ software including validation documentation development, review and execution
  • Maintain global clinical trial database standards (CDISC)
Requirements
  • Bachelor’s degree in a related field preferred
  • 3 years of clinical data management experience
  • Ability to program using SQL required
  • Experience with EDC systems (i.e. Veeva CDMS, Medidata RAVE, etc.)
  • Experience with Veeva EDC and Veeva CDB preferred
  • Proficient computer skills with understanding of clinical systems and data administration
  • Must be organized, an effective written and oral communicator
  • Must have the ability to multi-task, within a fast-paced environment, and build strong relationships

Celerion Values: Integrity Trust Teamwork Respect

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, protected veteran status, or disability.

Seniority level
  • Mid-Senior level
Employment type
  • Contract
Job function
  • Engineering and Information Technology
Industries
  • Biotechnology Research, Pharmaceutical Manufacturing, and Research Services
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