Are you passionate about clinical research data management and ensuring top-notch quality control in pharma? The EDC Coordinator position offers an exciting opportunity to support clinical trials by managing electronic data capture (EDC) systems, resolving queries, and maintaining data accuracy. Based in India’s thriving pharma sector, this full-time role (ID 2025-2876) is perfect for professionals with a background in life sciences or healthcare, looking to advance in clinical research quality control jobs. Join a dynamic team optimizing workflows for regulatory compliance and data integrity in clinical trials.
Responsibilities
As an EDC Coordinator in quality control, you’ll play a pivotal role in clinical research data management. Key duties include:
- Supporting clinical research site staff with accurate data entry, query resolution, and validation checks to ensure high data quality in EDC systems.
- Ensuring all data management processes adhere to Good Clinical Practice (GCP), FDA, and sponsor-specific regulations for compliance in clinical trials.
- Monitoring data discrepancies, performing data cleaning activities, and optimizing electronic data workflows.
- Collaborating with clinical research teams, sponsors, and IT teams to enhance data collection, reporting, and security in pharma quality control.
- Identifying and resolving EDC system issues, escalating to vendors or IT teams as needed for seamless operations.
- Performing other duties as assigned to support overall clinical research objectives.
Qualifications
To excel in this EDC Coordinator job in clinical research quality control, candidates should possess:
Required Skills/Abilities
- Strong understanding of clinical trial data collection, GCP guidelines, and regulatory requirements like FDA and IRB.
- Excellent analytical skills and attention to detail for ensuring data accuracy and compliance in EDC systems.
- Ability to work independently and collaboratively in a fast-paced clinical research setting.
Education and Experience
- High school diploma required; Bachelor’s degree or technical degree in life sciences, healthcare, or related field preferred.
- Strong attention to detail, organizational skills, and ability to follow protocols; familiarity with research regulations (GCP, IRB, FDA) is a plus.
- 1-2 years of experience in clinical research, healthcare, or laboratory settings, with exposure to data management in pharma.
Benefits
This full-time EDC Coordinator position offers competitive perks to support your career in clinical research quality control:
- Comprehensive health insurance and wellness programs.
- Opportunities for professional development in GCP and EDC training.
- Flexible work hours in a collaborative pharma environment.
- Paid time off, retirement plans, and performance bonuses.
