Senior Clinical Data Associate – Worldwide Clinical Trials
Worldwide Clinical Trials is hiring for the role of Senior Clinical Data Associate for its clinical data management team in India. This full-time opportunity is open for candidates based in Kochi or Trivandrum and involves collaboration with global study teams across multiple time zones. The role is suitable for professionals with experience in clinical data management, data cleaning, query resolution, database quality review and clinical trial documentation.
As a Senior Clinical Data Associate, the selected candidate will support high-quality clinical research by helping ensure the accuracy, completeness and integrity of clinical trial data. The position includes close coordination with Clinical Data Managers, internal study teams, cross-functional stakeholders and external partners to support reliable data delivery for research and development programs.
Job Overview
| Company | Worldwide Clinical Trials |
| Position | Senior Clinical Data Associate |
| Job Requisition ID | JR103116 |
| Job Type | Full time |
| Work Mode | Hybrid; onsite office travel required for the first 6 months |
| Location | Kochi / Trivandrum |
| Application Mode | Online Application |
Key Responsibilities
- Manage and execute data cleaning activities, including query review, query resolution and database page review activities.
- Support Clinical Data Managers with study deliverables such as Data Management Plans, CRF reviews, eCRF completion guidelines and Data Transfer Agreements.
- Prepare and distribute study-specific data management metrics to internal and external stakeholders.
- Conduct User Acceptance Testing of Electronic Data Capture systems to support database quality and readiness.
- Review and reconcile third-party vendor data to ensure consistency and accuracy across study datasets.
- Perform Database Quality Assessments, identify data trends and support training initiatives to improve team performance.
- Review SAS listings and data checks, investigate issues and resolve them through appropriate query management.
- Mentor and train Clinical Data Associates while coordinating study-related activities across the team.
- Support end-of-study activities, including preparation and oversight of study archival media and associated tracking processes.
Required Qualifications
- Bachelor’s degree or higher in Biomedical Sciences, Life Sciences, Computer Science or a related discipline.
- Equivalent relevant experience may also be considered as stated by the employer.
Experience Required
Candidates should have a minimum of 2 years of relevant clinical data management or related industry experience.
Required Knowledge and Skills
- Knowledge of clinical data management processes and technologies used in clinical trials.
- Understanding of clinical trial documentation, including protocols, statistical analysis plans, case report forms and study reports.
- Experience in reviewing and resolving clinical data queries and supporting database quality activities.
- Strong attention to detail with the ability to manage multiple priorities and maintain data accuracy.
- Effective written and verbal communication skills for collaboration across cross-functional teams.
- Proficiency in English.
Why This Role Is a Good Opportunity
This role offers the opportunity to contribute to clinical research data quality within a global CRO environment. The position involves meaningful participation in clinical trial data review, database readiness, quality assessments and study close-out support. Candidates with clinical data management experience can also gain exposure to global teams, cross-functional study processes and mentoring responsibilities.
How to Apply
Interested candidates can apply online through the official Worldwide Clinical Trials application link provided below.
