Job description

Role & responsibilities:

- 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.

📌 Clinical Data Management (Chennai)
🏢 Desirous Global Consulting
📍 Chennai