Centralized Study Analyst

We are looking for a highly skilled and experienced Centralized Study Analyst to join our team at a reputed pharmaceutical company in the Pharmaceutical & Life Sciences industry. The ideal candidate will have a strong background in clinical trial management and analysis, with excellent analytical and problem-solving skills.

Roles and Responsibility

• Manage and analyze clinical trial data to ensure accuracy and compliance with regulatory requirements.
• Coordinate with cross-functional teams, including project managers, biostatisticians, and medical writers, to ensure timely and successful study delivery.
• Develop and maintain databases and systems to track and manage study data.
• Conduct quality control checks on study data to identify and resolve issues.
• Collaborate with stakeholders to develop and implement process improvements.
• Provide training and support to junior staff members on study procedures and protocols.

Job Requirements

• Bachelor's degree in life sciences or a related field.
• Minimum 2 years of experience in clinical trial management and analysis.
• Strong knowledge of Good Clinical Practice (GCP) principles and regulations.
• Experience with clinical trial management systems (CTMS) and electronic data capture (EDC).
• Excellent analytical, problem-solving, and communication skills.
• Ability to work independently and as part of a team.