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Worldwide Clinical Trials Hiring for CDM

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Clinical Data Manager

Worldwide Clinical Trials

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences or Relvant degree

Kochi and Trivandrum

3 Years+

Verified Job

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Worldwide Clinical Trials is hiring a Clinical Data Manager for its clinical research operations in Kochi and Trivandrum, Kerala. This is a full-time, hybrid position focused on overseeing clinical data management activities across complex global clinical trials and ensuring accurate, timely project delivery.

Candidates with a bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, along with at least three years of relevant experience, can apply.

Worldwide Clinical Trials Recruitment 2026 – Job Details

ParticularsDetails
CompanyWorldwide Clinical Trials
Job TitleClinical Data Manager
Job Requisition IDJR103235
LocationsKochi and Trivandrum
Work ArrangementHybrid
Job TypeFull-time
ExperienceMinimum 3 years
QualificationBachelor’s degree or higher in a relevant discipline, or equivalent relevant experience
IndustryPharmaceutical, biotechnology, or medical device industries

Position

Clinical Data Manager

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The Clinical Data Manager oversees clinical data management activities from study start-up through conduct and close-out, ensuring data quality, timely database lock, appropriate resource allocation, and compliance with project timelines and budgets.

Key Responsibilities

  • Clinical Data Management Oversight: Manage data management activities across multiple complex global clinical trials and programmes.
  • Trial Documentation: Prepare Data Management Plans (DMPs), database specifications, edit check specifications, CCGs, and DTAs.
  • Data Quality and Cleaning: Oversee data cleaning activities and ensure effective User Acceptance Testing (UAT).
  • Vendor Reconciliation: Develop external vendor reconciliation specifications for Serious Adverse Events, IRT, and central laboratory data.
  • Database Lock: Ensure database lock activities are completed within established timelines.
  • Project Monitoring: Track project metrics, scope, budgets, risks, and progress, escalating concerns to Data Management leadership.
  • Stakeholder Collaboration: Represent the Data Management team in internal and external study meetings and coordinate with cross-functional teams.
  • Process Improvement: Participate in and lead process reviews and provide improvement recommendations to management and subject matter experts.

Eligibility and Qualifications

Candidates applying for the Worldwide Clinical Trials Clinical Data Manager position must meet the following requirements:

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  • Educational qualification: Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a related discipline.
  • Alternative qualification: Equivalent relevant experience.
  • Work experience: At least three years in clinical data management or a related role.
  • Relevant industries: Pharmaceutical, biotechnology, or medical device industries.

Required Skills

  • Excellent attention to detail.
  • Strong written and verbal communication skills.
  • Working knowledge of clinical data management best practices and technologies.
  • Understanding of clinical trial processes and protocols.
  • Familiarity with clinical trial documents, including protocols, statistical analysis plans, Case Report Forms (CRFs), and study reports.
  • Ability to collaborate with internal and external cross-functional teams.
  • Analytical thinking and problem-solving skills
APPLICATION DETAILS

How to apply

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