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Open nowPosted yesterday

Senior Clinical Data Associate

Worldwide Clinical Trials233 open roles

Where
Kochi
Work mode
Hybrid
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Your applicationOpen nowSenior Clinical Data AssociateWorldwide Clinical Trials · Kochi

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  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Worldwide Clinical Trials's own form.

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The clock on this job

Early applications get read.

13.8% of postings close within 7 days. Measured by our own scanner across the market. Worldwide Clinical Trials postings stay open a median of 43 days.

Share of postings closed within
  1. 2.2%1 day
  2. 4.7%3 days
  3. 13.8%7 days
  4. 22.3%14 days
  5. 37.8%30 days
  6. 59.0%60 days
This job: posted yesterday

Worldwide Clinical Trials median: 43 days open

The posting

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world.

With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research.

Make an Impact as a Senior Clinical Data Associate at Worldwide

Play a key role in ensuring the quality, accuracy, and integrity of clinical trial data that supports critical research and development programs. In this position, you will partner closely with Clinical Data Managers and cross-functional study teams to help deliver reliable data that drives confident decision-making.

You will take ownership of complex data review and cleaning activities, contribute to data management processes, and help maintain high standards across assigned studies. Your expertise will also support collaboration with internal and external stakeholders to ensure project objectives are met efficiently and accurately.

Beyond day-to-day study responsibilities, you'll have the opportunity to mentor junior team members, coordinate study activities, and contribute to continuous quality improvements within the clinical data management function.

Where You'll Work

This is a ONSITE role open to candidates based in Trivandrum/Kochi. You will collaborate with global teams across multiple time zones.

Travel to the office is required onsite for the first 6 months.

What You'll Do

  • Manage and execute data cleaning activities, including query review, query resolution, and database page review activities.
  • Support Clinical Data Managers with key study deliverables, including 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 (UAT) of Electronic Data Capture (EDC) systems to support database quality and readiness.
  • Review and reconcile third-party vendor data, ensuring consistency and accuracy across study datasets.
  • Perform Database Quality Assessments (DQA), identify data trends, and support training initiatives to improve team performance.
  • Review SAS listings and data checks, investigating and resolving issues 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.

What You'll Bring

  • Bachelor’s degree or higher in Biomedical Sciences, Life Sciences, Computer Science, or a related discipline, or equivalent relevant experience.
  • Minimum 2 years of relevant clinical data management or related industry experience.
  • 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 (CRFs), and study reports.
  • Experience 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 with the ability to collaborate across cross-functional teams.
  • Proficiency in English.

Discover the Difference

We love knowing that someone is going to have a better life because of the work we do. Discover the Difference at Worldwide Clinical Trials. Explore additional opportunities on our careers page, visit http://www.worldwide.com/careers, or connect with us on LinkedIn.

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