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Worldwide Clinical Trials

Contract research organization delivering clinical trials

Manager Clinical Database Programming

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in USA$99k - $196k /yr

About the Job

Requirements

  • A bachelor's degree or equivalent relevant education and experience is required.
  • Experience leading or managing clinical database programming activities within a clinical research environment is required.
  • Strong knowledge of electronic data capture systems, database configuration, validation, testing processes, and data management workflows is required.
  • Ability to review technical specifications, validation documentation, and database-related deliverables accurately is required.
  • Strong problem-solving skills and a methodical, logical approach to identifying and resolving issues are required.
  • Attention to detail and commitment to data quality and integrity are required.
  • Strong communication, collaboration, stakeholder management, and customer-focused relationship-building skills are required.
  • Proficiency in English and strong written and verbal communication skills are required.

Responsibilities

  • Lead, mentor, and develop a team of Clinical Database Programmers through performance management, training, and capability development.
  • Coordinate project assignments, timelines, and resource allocation to ensure high-quality and timely delivery of database programming activities.
  • Oversee electronic data capture development and database configuration activities across internal and third-party platforms.
  • Review database build specifications, edit check specifications, validation plans, and reconciliation requirements to ensure quality and compliance.
  • Partner with sponsors, internal stakeholders, and external vendors to resolve issues, implement system enhancements, and support electronic data transfers.
  • Guide database testing, validation, maintenance, and deployment activities in accordance with departmental procedures and standards.
  • Contribute to the development of database libraries, system documentation, procedures, and best practices.
  • Drive process improvements, provide technical leadership for new solutions, and support ongoing monitoring of study and system metrics.
  • Support quality assurance, audit readiness, and continuous improvement initiatives across Clinical Database Programming.

About the Company

Worldwide Clinical Trials

Contract research organization delivering clinical trials

Worldwide Clinical Trials is a contract research organization that provides drug development services for pharmaceutical and biotech companies, focusing on running clinical trials to bring new medicines to market. Its core work centers on the science and logistics of clinical trials—designing studies, coordinating sites and investigators, and managing data and regulatory processes to advance drug candidates through development. The company differentiates itself through its specialized, science-driven approach and global expansion achieved via strategic acquisitions, building a larger network and broader capabilities to support complex trial programs. After a history of ownership changes, including a re-launch in 2007 and a majority stake sale in 2023, the firm aims to grow further under new ownership while continuing to offer focused clinical trial services that support medical advancement.

Company size
1,001-5,000
Company stage
Acquired
Total funding
Not listed
Headquarters
Morrisville, NC
Founded
1986

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