Overseeing the collection, validation and processing of clinical trial data.
Developing and implementing data management procedures for clinical trials.
Supporting and facilitating the review of medical coding for validity and completeness.
Ensuring compliance with applicable regulations, protocols and standard operating procedures in India.
Maintain the highest data quality standards throughout the data lifecycle, from data collection to database lock.
Stay updated on industry best practices, technological advancements and regulatory requirements related to clinical data management.
Preferred candidate profile
Certification in clinical data management (like CCDM).
Knowledge of CRF design, MS Project and analytical capabilities.
Knowledge of CDISC standards and data interchange formats (e.g., SDTM, ADaM).
Familiarity with clinical trial design and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP).
Understanding of data privacy and protection regulations (e.g., GDPR).
Effective communication and interpersonal skills to collaborate with other teams.
Job Types: Full-time, Part-time, Permanent, Fresher
Pay: ₹25,000.00 - ₹33,000.00 per month
Expected hours: 24 per week
Benefits:
Flexible schedule
Food provided
Health insurance
Leave encashment
Provident Fund
Work Location: In person
Beware of fraud agents! do not pay money to get a job
MNCJobsIndia.com will not be responsible for any payment made to a third-party. All Terms of Use are applicable.