Are you a science enthusiast with a keen eye for detail and a passion for advancing healthcare? Do you dream of contributing to life-saving drug development without being at the lab bench? Then a career as a Clinical Data Associate (CDA) might be your perfect match!
This dynamic role is the backbone of clinical trials, ensuring the accuracy and integrity of the data that drives medical breakthroughs.
What Exactly Does a Clinical Data Associate Do? 🤔
Imagine a world where new medicines can’t reach patients because their trials are disorganized or the data is unreliable. That’s where you come in!
Clinical Data Associates are crucial in managing the vast amounts of information generated during clinical trials. You’ll be the guardian of data quality, working behind the scenes to ensure every piece of information is accurate, complete, and compliant with regulatory standards.
Your Key Responsibilities:
📅 Organizing & Monitoring Clinical Trials
Track progress across different trial phases and ensure documentation and updates are properly maintained.
📝 Collecting & Authenticating Data
Gather vital information from sources like scientific publications, reports, and trusted databases such as PubMed and ClinicalTrials.gov.
🕵️ Conducting Quality Checks
Review datasets and documents meticulously. Identify discrepancies and resolve queries to maintain 100% accuracy.
📈 Tracking Updates & Amendments
Monitor changes in trial protocols, safety reports, and regulatory updates.
🌐 Utilizing Clinical Systems
Work with eTMF platforms, data management tools, and Excel-based tracking systems.
Why Is This Role So Important? 🌟
Every successful drug and medical innovation depends on reliable clinical data. Clinical Data Associates ensure that this data is clean, compliant, and credible — enabling researchers and regulators to make informed decisions about safety and efficacy.
Your work directly contributes to:
- Faster drug approvals
- Improved patient safety
- Stronger regulatory submissions
- Advancement of healthcare globally
Current Opportunity: Join Ascentrik Research Services – Pune (Wakad)
📍 Location: Pune (Wakad)
💼 Role: Clinical Data Associate
📊 Vacancies: 5
💰 Salary: ₹1.5–2 LPA
🎯 Experience: 0–1 year
Who Can Apply? 🎓
🎓 Preferred Qualification:
- M.Pharm (Pharmaceutics, Pharmacology preferred)
- M.Sc. (Biotechnology, Biochemistry, Molecular Biology, Microbiology, Clinical Research, Drug Development, Genetics, Immunology, etc.)
🚫 Not Eligible:
- M.Pharm (Pharmacognosy major)
- M.Sc. (Botany, Zoology, Environmental Science, Ecology majors)
📘 Bachelor’s Degree Holders:
If you hold a B.Pharm and have at least 1 year of relevant experience in:
- Clinical Research
- Clinical Data Management
- Pre-Clinical Research
- Drug Development
- Medical Writing
You are encouraged to apply!
Must-Have Skills 💪
✔ Clinical Data Management fundamentals
✔ Strong understanding of clinical trials
✔ Attention to detail
✔ Excel proficiency
✔ Documentation accuracy
Good-to-Have Skills 🌟
- Knowledge of eTMF systems
- Oncology & Immunology exposure
- Secondary research experience
- Published research paper
- PG Diploma in Clinical Research/CDM
- Excellent communication skills
- Deadline management ability
- Inquisitive & analytical mindset
Career Growth & Future Scope 🚀
A Clinical Data Associate role can lead to exciting career paths such as:
- Clinical Data Manager
- Clinical Project Coordinator
- Regulatory Affairs Specialist
- Clinical Research Associate (CRA)
- Pharmacovigilance Associate
With experience, professionals in Clinical Data Management can earn significantly higher packages and transition into leadership roles in CROs, pharmaceutical companies, and biotech firms.
Why Choose This Career?
✔ Work at the forefront of medical innovation
✔ High demand in pharma & CRO sectors
✔ Strong career progression
✔ Meaningful contribution to global healthcare
✔ Blend of science + data + research
If you’re passionate about science, detail-oriented, and ready to build a rewarding career in clinical research, this is your opportunity!
