Are you looking to build a career in Clinical Data Management (CDM) within the clinical research industry? Here’s an exciting full-time hybrid opportunity for the role of Associate Clinical Data Coordinator available in Kochi, Mumbai, and Bangalore, India. 🚀
This opportunity is ideal for candidates interested in clinical trial data management, sponsor collaboration, and global research operations.
Clinical Data Management plays a critical role in ensuring the accuracy, integrity, and regulatory compliance of clinical trial data, which directly impacts drug approvals and healthcare advancements.
📍 Job Locations
- Kochi, India
- Mumbai, India
- Bangalore, India
Work Model: Hybrid
Employment Type: Full-Time
These locations are major hubs for clinical research organizations (CROs) and pharmaceutical companies, providing strong career exposure and networking opportunities. 🌍
💼 Job Role: Associate Clinical Data Coordinator
As an Associate Clinical Data Coordinator, you will support clinical data teams in managing and maintaining high-quality datasets for clinical trials.
This role requires strong attention to detail, analytical thinking, and effective collaboration with project teams and sponsors.
Your work will help ensure that clinical trial data remains accurate, compliant, and ready for regulatory submissions.
🔎 Key Responsibilities
📌 Data Cleaning & Quality Checks
- Perform regular data cleaning activities
- Verify accuracy and completeness of clinical datasets
- Deliver clean and validated datasets to sponsors within deadlines
Clean data is essential for reliable clinical trial results and regulatory approvals.
📌 Project Coordination
- Assist the Data Manager in study-related activities
- Coordinate with cross-functional teams
- Support smooth workflow across departments
Strong communication helps maintain efficient study timelines. 🤝
📌 Backup & Support Role
- Provide support to Senior Data Coordinators or Team Leads
- Handle assigned tasks independently when required
- Maintain accountability for deliverables
This responsibility allows professionals to gain leadership exposure early in their careers.
📌 Quality & Compliance
- Ensure project deliverables meet quality standards and sponsor expectations
- Participate in internal study meetings
- Attend sponsor or internal audits
- Stay updated with training requirements and eSOP guidelines
Compliance with GCP standards is critical in clinical research. 📑
📌 Risk Tracking & Issue Resolution
- Track study progress and project milestones
- Identify potential risks or delays
- Take corrective actions with guidance from the Data Team Lead (DTL)
Proactive problem-solving ensures smooth project execution. 🔍
🎓 Eligibility Criteria
Ideal candidates usually have:
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field
- Basic understanding of Clinical Data Management
- Familiarity with clinical trial processes
- Strong communication and analytical skills
- Ability to work effectively in a team environment
Fresh graduates with relevant internships or 1–2 years of clinical research experience are encouraged to apply.
💡 Required Skills
✔ Attention to detail
✔ Analytical thinking
✔ Communication and teamwork
✔ Knowledge of data cleaning and validation processes
✔ Understanding of GCP guidelines (preferred)
🌱 Career Growth Opportunities
Starting as an Associate Clinical Data Coordinator can lead to multiple career paths within the clinical research field:
- Clinical Data Coordinator
- Senior Data Coordinator
- Data Team Lead (DTL)
- Clinical Data Manager
- Clinical Project Manager
Clinical Data Management is one of the fastest-growing sectors in pharmaceutical research, driven by increasing global clinical trials and regulatory requirements. 📈
🌍 Why Apply for This Role?
✨ Hybrid work flexibility
✨ Exposure to global sponsors
✨ Career growth in clinical research
✨ Participation in audits and regulatory processes
✨ Hands-on experience in clinical trial data lifecycle
Mumbai and Bangalore are major pharmaceutical and IT hubs, while Kochi is emerging as a growing center for clinical research operations.
🔗 Apply Here
Kochi:
https://jobs.iqvia.com/en/jobs/R1524135-0
Bangalore:
https://jobs.iqvia.com/en/jobs/R1524135-1
Mumbai:
https://jobs.iqvia.com/en/jobs/R1524135-2
📝 Final Thoughts
If you are passionate about clinical research and data accuracy, the Associate Clinical Data Coordinator role offers an excellent platform to build your expertise in clinical data management and regulatory compliance.
With openings across Kochi, Mumbai, and Bangalore, this opportunity provides geographical flexibility, industry exposure, and long-term career growth. 🌟
Start your journey in clinical research and contribute to advancing global healthcare through reliable clinical trial data.
