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Worldwide Clinical Trials

Contract research organization delivering clinical trials

Clinical Programming Manager

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeNo salary listedIn-person

About the Job

Requirements

  • Be educated to degree level or have relevant experience.
  • Have at least 2 years of management experience.
  • Have at least 8 years of experience with Data Management Systems and Software.
  • Understand Clinical Data Interchange Standards Consortium Study Data Tabulation Model standards.
  • Have experience with the SAS programming language.
  • Demonstrate written and verbal communication skills, a methodical and logical approach to problem solving, attention to detail, willingness to question data validity, teamwork, customer focus, delivery on commitments, relationship building, communication and influencing, innovation and change, computer literacy, numeracy, and adaptability to various computer systems.

Responsibilities

  • Manage and develop the performance of Clinical Database Programmers through performance management, capability building, training, and development.
  • Liaise with relevant staff to allocate tasks, establish timelines, report progress, and identify outstanding issues.
  • Assess the technical merits and development of, and changes to, internal and third-party software applications and databases.
  • Manage allocated electronic data capture development work to achieve timely delivery.
  • Review specifications for setting up and modifying project-specific data-entry software, including edit-check specifications.
  • Review validation plans for edit-check and reconciliation-check specifications.
  • Configure internal and third-party database and electronic data capture software for Data Management, sponsors, and sites.
  • Test databases and related applications according to Information Technology and Data Management standard operating procedures for initial setup and maintenance.
  • Run database upload programs and process error reports.
  • Liaise with third-party vendors to resolve issues and implement software changes.
  • Liaise with sponsors or their designates regarding electronic data transfers to or from the company.
  • Develop and maintain database libraries in assigned applications.
  • Participate in planning, progress reporting, system monitoring, and study metrics monitoring.
  • Contribute to the development and technical leadership of new processes and implementation of new solutions.
  • Support Data Management in producing and maintaining system procedures and documentation in accordance with applicable standard operating procedures.
  • Assist with Quality Assurance and audit requirements.
  • Perform other duties as assigned.

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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