If you’re a recent post-graduate in Pharmacy, Biotech, or Chemistry looking to enter the clinical research field, your opportunity has arrived. Ascentrik Research Pvt. Ltd.—a trusted name in research analytics—is hiring freshers for Clinical Data Management roles in Pune. This is an exciting entry-level opportunity to work with a globally respected firm and contribute to life-saving clinical studies.
🧬 About Ascentrik Research Pvt. Ltd.
With offices in Pune, Navi Mumbai, and Noida, Ascentrik Research is a data-driven research solutions company that delivers customized analytics to top Fortune 500 companies and multinational clients across healthcare and pharma sectors. Known for its high-quality research services and clinical intelligence, Ascentrik has built a strong reputation in clinical data management, oncology studies, and regulatory support.
This organization doesn’t just offer a job—it offers a structured launchpad for building your clinical research career in a globally competitive environment.
💼 Job Role: Clinical Data Associate (Entry-Level)
🏙️ Location: Pune, Maharashtra
🕐 Experience: 0 – 1 Years (Freshers Welcome)
🎓 Qualification: M.Pharm, MSc (Chemistry, Biochemistry, Biotechnology)
🔍 Job Type: Full-Time, Onsite
💰 Perks: Work-life balance, challenging tasks, career mentorship, insurance
🧾 Key Responsibilities
As a Clinical Data Associate, your primary responsibility is to handle, verify, and analyze clinical trial data from various sources. This is a foundational role in any drug development process.
Here’s what you’ll be doing:
- 🧪 Organize and track all clinical trial phases, ensuring timelines are met and data is accurate.
- 📚 Collect and verify data from journals, clinical databases, conferences, and public repositories like PubMed and ClinicalTrials.gov.
- ✅ Conduct 100% quality checks on documents before final submission.
- 🔍 Track updates related to drug trials, safety outcomes, biomarkers, and efficacy results.
- 📊 Ensure all trial-related insights are in compliance with clinical safety and performance standards.
- 🧠 Work under deadlines and manage multiple data tasks simultaneously.
This role provides real-world exposure to data handling in the pharmaceutical and life sciences industries—critical for anyone wanting to progress into clinical research, medical writing, pharmacovigilance, or regulatory affairs.
🎓 Required Skills & Qualifications
To succeed in this role, candidates must bring academic knowledge and basic technical competency to the table. Here’s what’s expected:
- 📘 A Master’s degree in Pharmacy, Chemistry, Biochemistry, or Biotechnology.
- 👩🎓 Fresh graduates or those with up to 1 year of experience in clinical data handling or research roles.
- 🔬 Familiarity with clinical trial design, medical terms, and oncology studies is a bonus.
- 🌐 Understanding of research tools like PubMed, ClinicalTrials.gov, and scientific journal databases.
- 💬 Strong communication and organizational skills for handling internal documentation and reporting.
- 💻 Good command over Microsoft Office and basic internet research techniques.
- 🏆 Additional certifications in clinical research or GCP (Good Clinical Practices) will be an added advantage.
🌟 Why Join Ascentrik Research?
Joining Ascentrik Research as a fresher gives you direct access to live projects involving real-world data from clinical studies. Unlike many entry-level jobs that restrict roles to observation, Ascentrik lets you work on important data workflows from the beginning.
Here’s why it’s a great choice:
✔ Freshers Accepted: No need to worry about 2-3 years’ experience clauses. If you’re trained and passionate, you’re welcome.
✔ Fortune 500 Client Exposure: Get hands-on experience on projects used by global pharma and biotech giants.
✔ Career Growth: Strong mentorship and upskilling pathways within the firm—perfect for moving into senior roles or specialized areas.
✔ Work Culture: Fast-paced but friendly—ideal for learning and collaboration.
✔ Healthcare Impact: Every dataset you work on contributes to drug development that may save lives.
🧭 Career Growth & Next Steps
Once you gain 1–2 years of experience in this role, you can grow into more advanced positions such as:
- Clinical Data Analyst
- Clinical Project Coordinator
- Regulatory Affairs Associate
- Medical Writer
- Pharmacovigilance Specialist
This foundational job also prepares you for international clinical trials, regulatory documentation, and future certifications like CCRP, GCP, or ICH.
📌 Is This Job Right for You?
This role is perfect for you if:
✅ You are a postgraduate in life sciences with strong academic performance.
✅ You are familiar with the basics of clinical research and medical terminologies.
✅ You want to gain real-world pharma exposure with global clients.
✅ You are looking for a long-term career in healthcare data, research, or regulatory affairs.
✅ You are comfortable working with deadlines and multitasking.
💬 Final Thoughts
Starting your career in clinical data management at a company like Ascentrik Research is not just a smart move—it’s a strategic one. With industry exposure, mentorship, and impactful projects, you’ll gain both the skills and the confidence needed to thrive in the life sciences industry.
Whether your ultimate goal is clinical trials, pharmacovigilance, regulatory writing, or biotech analytics, this job sets you on the right path from day one.
If you’re passionate about healthcare innovation, research integrity, and making a real-world impact—this is your cue to get started.
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