Senior Clinical Data Associate

Roles and Responsibilities :

• Manage clinical trial data from various sources, ensuring accuracy, completeness, and compliance with regulatory requirements.
• Collaborate with cross-functional teams to resolve issues related to data quality, integrity, and timelines.
• Develop and maintain databases using CDM tools such as Veeva or RAVE for storing and analyzing clinical trial data.
• Ensure adherence to company policies, procedures, and industry standards for clinical data management.

Job Requirements :

• 3.9-5 years of experience in Clinical Data Management (CDM) or a related field.
• Strong understanding of GCP principles and regulations governing clinical trials.
• Proficiency in managing large datasets using CDM systems like Veeva or RAVE.