If you’re looking to build a strong career in clinical research and data management, here’s an exciting opportunity you shouldn’t miss! 🌟 The globally recognized CRO Medpace is expanding its footprint in India and hiring for the role of Data Coordinator – Core Laboratory at its Hyderabad office. This role is ideal for candidates with a Life Sciences or Pharmacy background who want to work on international clinical trials and gain global exposure.
🏥 About Medpace
Medpace is a full-service clinical contract research organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies worldwide. Known for its scientific-driven approach and operational excellence, Medpace plays a critical role in advancing drug development across Phase I to Phase IV trials.
With its growing presence in India, particularly in Hyderabad, Medpace is building a strong team of clinical research professionals. Joining at this stage offers candidates the opportunity to be part of a high-growth environment and contribute to global healthcare advancements.
📍 Job Location
Hyderabad, India 🌆
🎓 Eligibility Criteria
Candidates interested in applying should meet the following qualifications:
Bachelor’s or Master’s degree in:
Pharmacy (B.Pharm / M.Pharm)
Life Sciences (Biotechnology, Microbiology, Biochemistry, etc.)
Clinical Research or related field
⏳ Experience Required:
1 to 2 years in Clinical Data Management (CDM), CRO, or Pharma industry
This role is particularly suitable for professionals who already have some exposure to clinical trial data handling and are looking to step into a more global and structured work environment.
📝 Key Responsibilities
As a Data Coordinator – Core Laboratory, your day-to-day work will involve managing and ensuring the quality of clinical trial data. Key responsibilities include:
📊 Data Management & Validation
Handling data transfers from core laboratories
Validating datasets to ensure accuracy and completeness
🔍 Data Cleaning & Query Resolution
Identifying inconsistencies or missing data
Raising and resolving queries with stakeholders
📁 Documentation & Compliance
Maintaining study-related documents
Ensuring adherence to ICH-GCP and regulatory standards
🌐 Cross-functional Collaboration
Working closely with global teams including clinical operations, biostatistics, and programming
This role requires strong attention to detail, analytical thinking, and the ability to work in a team-oriented environment.
🌟 Why You Should Consider This Opportunity
Joining Medpace offers several advantages that can significantly boost your career:
🌍 Global Exposure
Work on international clinical trials across multiple therapeutic areas
📈 Career Growth
Structured learning programs and clear career progression paths
🧠 Skill Development
Hands-on experience with clinical data systems and regulatory frameworks
🏢 Growing Organization in India
Be part of a rapidly expanding team in Hyderabad
🤝 Collaborative Work Culture
Opportunity to interact with experts across the globe
📩 How to Apply
Interested candidates can apply directly through the official careers page:
🔗 https://careers.medpace.com/jobs/11923
Make sure your resume highlights relevant experience in clinical data management, data cleaning, and any exposure to clinical trials or regulatory compliance.
💡 Tips for Applicants
✔️ Tailor your CV with keywords like “Clinical Data Management,” “ICH-GCP,” and “Data Validation”
✔️ Mention any tools you’ve used (e.g., EDC systems, Excel, SAS basics if applicable)
✔️ Highlight teamwork and communication skills
✔️ Be ready to discuss your previous project experience in interviews
🧾 Final Thoughts
This opportunity with Medpace is ideal for candidates who want to transition into a globally aligned clinical research role. With Hyderabad emerging as a major hub for CROs and pharmaceutical companies, this position offers both stability and growth.
If you meet the criteria and are passionate about clinical research, don’t wait—apply now and take a step forward in your career! 🚀
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