Are you passionate about clinical data, quality assurance, and cutting-edge research? A career as a Senior Data Monitoring Coordinator at Labcorp might just be the opportunity you’ve been waiting for! Based in Bangalore, this role offers you the chance to work at a global life sciences company that’s deeply committed to transforming healthcare through innovation and collaboration.
🏢 About Labcorp
Labcorp is a leader in the global life sciences space, offering advanced diagnostic solutions and drug development services. The company plays a vital role in helping medical professionals, hospitals, and research organizations make better decisions for patient care. Their mission is simple but powerful — “to improve health and improve lives.”
An inclusive work environment, diverse teams, and a culture that supports growth and wellbeing define the workplace at Labcorp. As an Equal Opportunity Employer, Labcorp welcomes candidates from all walks of life.
👩⚕️ About the Role: Senior Data Monitoring Coordinator
If you have a background in Life Sciences, Pharmacy, or Clinical Research and are interested in the field of data quality and compliance, this position is tailored for you. The Sr. Data Monitoring Coordinator will work closely with cross-functional teams and take responsibility for validating and maintaining the integrity of clinical trial data.
🧾 Key Responsibilities
This role isn’t just about working behind a screen — it’s about contributing to impactful projects in the healthcare ecosystem. Here’s what your core responsibilities would include:
- Monitoring clinical trial data to ensure accuracy, completeness, and reliability.
- Validating entries against regulatory standards such as ICH-GCP, FDA, and EMA protocols.
- Collaborating with teams like data managers, biostatisticians, and clinical research associates to resolve discrepancies.
- Preparing data review and discrepancy reports regularly.
- Maintaining documentation and audit trails to ensure traceability.
- Supporting database lock procedures and performing final reviews.
- Identifying patterns or trends in data inconsistencies.
📚 Qualifications and Skills Needed
To qualify for this opportunity, candidates need to bring a blend of academic background and technical skills:
- Educational Qualification: B.Pharm, M.Pharm, Pharm.D, MSc, or BSc in Life Sciences
- Experience: 6 months to 2 years in clinical data management or monitoring
- Hands-on knowledge of EDC platforms like Medidata Rave or Oracle Clinical
- Understanding of industry standards like CDISC, SDTM, and CDASH
- Strong analytical and troubleshooting skills
- Excellent attention to detail and documentation practices
- Good communication skills for cross-functional collaboration
💼 Why Choose Labcorp?
Choosing where you work isn’t just about the salary. It’s about the experience, the growth, and the impact you can create. Here’s why Labcorp stands out:
🌐 Global Reach
Labcorp’s solutions influence healthcare systems worldwide. By joining them, you’re not just building a career — you’re contributing to life-saving innovations.
📈 Career Progression
Labcorp encourages internal mobility, offers professional training programs, and provides clear pathways to help you advance your career.
🧑🤝🧑 Inclusive Culture
Whether you’re a fresher or a working parent, Labcorp’s inclusive policies create an environment where you can thrive professionally and personally.
⏰ Work-Life Balance
With flexible work schedules and competitive compensation packages (around ₹4–6 LPA), this role supports a balanced and fulfilling lifestyle.
🏙️ Job Location & Work Conditions
This role is based out of Bangalore, India — a growing hub for clinical research and data sciences. The environment is dynamic, professional, and fast-paced. Expect to work on challenging yet rewarding projects that keep you engaged and motivated.
🔍 Who Should Apply?
This role is ideal for:
- Recent graduates or early professionals looking to enter the clinical trials industry
- People passionate about data quality, compliance, and patient safety
- Candidates aiming for a stable yet growth-oriented career in life sciences
- Anyone with attention to detail, strong reporting skills, and a keen eye for regulatory protocols
🧭 Career Path After This Role
Once you’re in as a Sr. Data Monitoring Coordinator, you can branch out into roles like:
- Clinical Data Manager
- Lead CRA
- Regulatory Specialist
- Clinical Operations Manager
- Or even transition into areas like Medical Writing or Pharmacovigilance
Labcorp supports this horizontal and vertical movement within departments through regular upskilling programs and mentorship.
💬 What Makes This Role Special?
- You’re not just entering data; you’re guarding the integrity of clinical research.
- You work closely with real-world data that shapes regulatory submissions.
- You’re part of a mission that directly connects to public health improvements.
✨ Final Thoughts
A career as a Senior Data Monitoring Coordinator at Labcorp is more than just a job — it’s a chance to make an impact in the evolving world of healthcare and clinical research. If you’re someone with a scientific background and a strong eye for detail, this role could be your stepping stone into a meaningful and prosperous career.
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