Senior Clinical Data Co-ordinator Wanted at Worldwide Clinical

Worldwide Clinical Trials Recruitment – Senior Clinical Data Co-ordinator

Worldwide Clinical Trials is hiring a Senior Clinical Data Co-ordinator for its Clinical Data Management team in India. The full-time, on-site opportunity is available in Kochi and Trivandrum, Kerala. Candidates with at least five years of experience in data management systems and software, knowledge of CDISC SDTM standards, and SAS programming experience can apply. The role involves clinical database configuration, validation, SAS programming, data reconciliation, and coordination with sponsors and clinical data management teams.

Company Overview

Worldwide Clinical Trials is a global contract research organization (CRO) with more than 3,500 professionals working to support clinical research and improve patient outcomes. The company focuses on delivering clinical trial services through quality, innovation, collaboration, and scientific expertise.

Job Details

Job Role & Responsibilities

The Senior Clinical Data Co-ordinator will coordinate and perform activities related to the configuration, maintenance, and validation of clinical databases, database systems, and associated applications.

Key responsibilities include:

• Coordinate with relevant staff to allocate tasks, establish timelines, report progress, and communicate outstanding issues.

• Assist in training and mentoring Clinical Database Programmers in database configuration and SAS program development, testing, and execution.

• Support Data Management staff in preparing database and SAS program specifications.

• Review specifications for setting up and modifying project-specific data entry software, including edit checks.

• Review validation plans for edit checks and reconciliation checks.

• Develop, test, and run SAS programs for clinical data management, including data validation, reconciliation checks, data listings, and data transfers.

• Configure internal and third-party electronic data capture (eDC) and database software for Data Management teams, sponsors, and clinical sites.

• Test databases and related applications according to IT and Data Management departmental standard operating procedures (SOPs).

• Execute database upload programs and process error reports.

• Coordinate with third-party vendors to resolve issues and implement software changes.

• Communicate with sponsors or their representatives regarding electronic data transfers.

• Support the preparation and maintenance of system procedures and documentation in accordance with applicable SOPs.

• Assist with quality assurance activities and audit requirements.

• Perform other duties as assigned.

Eligibility & Qualifications

Candidates should meet the following requirements:

• Education: Degree-level education or relevant experience.

• Experience: At least 5 years of experience working with data management systems and software.

• Clinical Data Standards: Understanding of CDISC SDTM standards.

• Programming Skills: Experience with the SAS programming language.

Required Skills & Competencies

Applicants should demonstrate the following skills:

• Good written and verbal communication skills.

• A methodical and logical approach to problem-solving.

• Ability to learn new tasks quickly and adapt to different computer systems.

• Strong attention to detail and a questioning approach to data validity.

• Good numerical and computer literacy.

• Ability to work efficiently and collaboratively.

• Customer focus and commitment to delivering on responsibilities.

• Relationship-building, communication, and influencing skills.

• Willingness to embrace innovation and organizational change.

Work Location

The position is listed as on-site and is available in:

• Kochi, Kerala

• Trivandrum, Kerala

This is a full-time opportunity with Worldwide Clinical Trials.

How to Apply

Interested and eligible candidates can apply through the official Worldwide Clinical Trials careers portal.

Apply for Senior Clinical Data Co-ordinator – Worldwide Clinical Trials

Applicants should review the official job description and ensure they meet the experience, CDISC SDTM, and SAS programming requirements before submitting their application.

Job Summary