are you looking to start or advance your career in clinical data management jobs in India? SIRO Clinpharm Pvt. Ltd., a leading global CRO, is hiring a Clinical Data Coordinator for a full-time remote role. This is a fantastic opportunity for graduates with experience in clinical trials, electronic data capture (EDC), and data review who want to work in a dynamic, regulatory-driven environment.
Key Responsibilities
As a Clinical Data Coordinator at SIRO Clinpharm, you will:
- Perform data review of clinical trial data, including query management.
- Review reconciliation of external data vs. EDC data.
- Assist in creating study documents, reports, and metrics.
- Support database lock activities (interim & final).
- File and maintain study documents in eTMF and project archives.
- Conduct quality reviews of eTMF documents.
- Document meeting minutes and track data management activities.
- Support inspection readiness during audits and regulatory inspections.
- Assist with data collection systems setup & testing.
- Ensure GxP compliance and SOP adherence.
Educational Qualifications & Experience
- Associate or Bachelor’s degree (Life Sciences, Pharma, Computer Science preferred).
- 1+ years of clinical data management experience (or equivalent training).
- Familiarity with EDC systems.
- Knowledge of FDA & ICH regulations, industry best practices, and data management standards preferred.
Skills & Competencies
- Strong attention to detail & organizational skills.
- Good time management and adaptability.
- Proficiency in Microsoft Office and data management tools.
- Excellent teamwork, problem-solving, and interpersonal skills.
Benefits of Joining SIRO Clinpharm
- Opportunity to work in a global CRO environment.
- Exposure to end-to-end clinical trial data management.
- Remote flexibility with corporate training and mentorship.
- Growth opportunities in clinical research & pharmacovigilance domains.
