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Worldwide Clinical Trials

Contract research organization delivering clinical trials

Senior Clinical Programmer

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeKochi, Kerala, IndiaNo salary listedHybrid

About the Job

Requirements

  • Be educated to degree level or have relevant experience.
  • Have at least 5 years of experience with data management systems and software.
  • Understand CDISC SDTM 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, questioning of data validity, teamwork, computer literacy, numeracy, and willingness to adapt to various computer systems.

Responsibilities

  • Coordinate and perform processes associated with the configuration, maintenance, and validation of databases, database systems, and associated applications.
  • Liaise with relevant staff to allocate tasks, establish timelines, report progress, and identify outstanding issues.
  • Assist in training and mentoring Clinical Database Programmers in database configuration and the development, testing, and execution of SAS programs.
  • Assist in training and mentoring Data Management staff in database and SAS program specification.
  • Review specifications for the setup and modification of project-specific data-entry software, including edit-check specifications.
  • Review validation plans for edit-check and reconciliation-check specifications.
  • Develop, test, and run SAS programs for clinical data management, including data validation and reconciliation checks, data listings, and data transfers.
  • Configure internal and third-party electronic data capture software for Data Management, sponsors, and sites.
  • Test databases and related applications according to Information Technology and Data Management departmental 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 the transfer of electronic data to or from the company.
  • 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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