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Ascentrik Research Services Hiring Clinical Data Associate in Pune

If you are searching for Clinical Data Associate jobs in Pune and want to build a long-term career in Clinical Research and Clinical Data Management, then this opportunity from Ascentrik Research Services could be worth exploring. The company is currently hiring Clinical Data Associates at its Wakad, Pune office and is looking for candidates from Pharmacy, Biotechnology, Clinical Research, Biochemistry, Genetics, Molecular Biology, and related Life Sciences backgrounds.

Clinical Data Management is one of the fastest-growing domains within the pharmaceutical and clinical research industry. As the number of global clinical trials continues to increase, organizations require skilled professionals who can collect, validate, organize, and analyze clinical data accurately. This role provides an excellent entry point for fresh postgraduates and professionals with up to one year of experience who want to gain exposure to drug development, clinical trials, scientific research, and healthcare analytics.

📌 Job Overview

Particulars Details
Position Clinical Data Associate
Company Ascentrik Research Services
Location Wakad, Pune, Maharashtra
Experience 0–1 Year
Vacancies 5
Employment Type Full-Time, Permanent
Salary ₹1.5 – ₹2.0 LPA
Industry Healthcare, Clinical Research & Life Sciences

🏢 About Ascentrik Research Services

Ascentrik Research Services works in the healthcare and life sciences research domain and supports scientific research initiatives through data collection, validation, analysis, and clinical intelligence activities. The organization focuses on delivering high-quality research outputs while maintaining strict quality standards and timelines.

For fresh graduates, this role provides valuable exposure to real-world clinical research projects and helps develop practical skills that are highly relevant across CROs, pharmaceutical companies, biotechnology firms, and healthcare consulting organizations.

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📋 Key Responsibilities

As a Clinical Data Associate, you will be responsible for supporting research and clinical trial activities through data collection, validation, monitoring, and quality review processes.

  • Organize and monitor different phases of clinical trials.
  • Track updates across ongoing clinical studies.
  • Collect scientific information from journals, conferences, and trial registries.
  • Validate clinical research data for quality and accuracy.
  • Perform quality checks before final submission.
  • Review efficacy, safety, biomarker, and bioavailability data.
  • Monitor developments across therapeutic areas such as oncology and immunology.
  • Conduct literature searches using PubMed and ClinicalTrials.gov.
  • Compile clinical trial information from multiple scientific sources.
  • Work within strict project timelines and quality standards.

🎓 Educational Qualifications

Candidates must possess a strong scientific background. Preferred qualifications include:

  • M.Pharm (Pharmaceutics, Pharmacology, or related disciplines)
  • M.Sc Biotechnology
  • M.Sc Biochemistry
  • M.Sc Molecular Biology
  • M.Sc Microbiology
  • M.Sc Clinical Research
  • M.Sc Drug Development
  • M.Sc Genetics
  • M.Sc Immunology

Additional Preferred Qualifications

  • Post Graduate Diploma in Clinical Research (PGDCR)
  • Post Graduate Diploma in Clinical Data Management
  • Published research paper in peer-reviewed journals
  • Knowledge of pre-clinical and clinical studies
  • Experience in secondary research activities

❌ Not Eligible

  • M.Pharm Pharmacognosy
  • M.Sc Botany
  • M.Sc Zoology
  • M.Sc Environmental Science
  • M.Sc Ecology

🧠 Skills Required

Apart from educational qualifications, candidates should possess the following skills:

  • Clinical Data Management knowledge
  • Clinical Research understanding
  • Clinical Trial Management awareness
  • eTMF knowledge
  • Scientific literature review expertise
  • PubMed searching skills
  • ClinicalTrials.gov database knowledge
  • Advanced Microsoft Excel proficiency
  • Strong analytical thinking
  • Problem-solving ability
  • Excellent written and verbal communication
  • Attention to detail and quality focus

🚀 Why Clinical Data Management is a Great Career Choice

Many freshers focus only on Pharmacovigilance, Regulatory Affairs, or Quality Assurance roles. However, Clinical Data Management has emerged as one of the most stable and growing career paths in the pharmaceutical industry.

Clinical Data professionals play a critical role in ensuring that data collected during clinical trials is accurate, complete, and regulatory compliant. Without high-quality clinical data, pharmaceutical companies cannot successfully evaluate the safety and effectiveness of new medicines.

The demand for Clinical Data Management professionals continues to increase due to the growth of global clinical trials, biotechnology research, and data-driven healthcare solutions.

🌟 Career Growth Opportunities

Professionals entering Clinical Data Management can build rewarding long-term careers within CROs, pharmaceutical companies, and biotechnology organizations.

Potential career progression may include:

  • Clinical Data Associate
  • Clinical Data Coordinator
  • Clinical Data Analyst
  • Clinical Data Management Executive
  • Clinical Data Manager
  • Lead Data Manager
  • Clinical Operations Specialist
  • Clinical Research Associate
  • Project Manager – Clinical Research

💰 Salary Information

According to the company notification, the offered salary range is:

₹1.5 – ₹2.0 LPA

While this may be considered an entry-level package, candidates can gain valuable industry experience that significantly improves future earning potential within Clinical Research and Data Management domains.

📝 How to Improve Your Chances of Selection

Candidates applying for Clinical Data Associate positions should focus on developing practical industry skills before attending interviews.

  • Learn basic Clinical Research concepts.
  • Understand Clinical Trial Phases.
  • Practice PubMed literature searches.
  • Learn ClinicalTrials.gov navigation.
  • Improve Microsoft Excel skills.
  • Study GCP (Good Clinical Practice) basics.
  • Review common Clinical Data Management terminology.
  • Prepare scientific literature review examples.

🔗 Application Link

📢 Final Thoughts

The Clinical Data Associate opportunity at Ascentrik Research Services offers an excellent starting point for Life Sciences, Pharmacy, Biotechnology, and Clinical Research professionals who want to enter the world of Clinical Data Management. The role provides exposure to clinical trials, scientific literature analysis, data validation, and research quality processes. For candidates looking to establish a career in Clinical Research and Drug Development, this opportunity can serve as a valuable first step toward long-term professional growth.

Vaibhav Totala
About Vaibhav
Vaibhav is the founder of Pharma Hiring Hub, a platform focused on Pharmacovigilance, Regulatory Affairs, Clinical Research, pharma careers, interview preparation and industry updates for life science professionals and freshers across India.
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