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 robust 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 complex statistical models and databases to support study design and analysis.
Collaborate with stakeholders to identify and resolve issues related to study conduct, data quality, or patient safety.
Prepare and review study reports, including protocol deviations,



adverse event reports, and final study reports.
Ensure compliance with Positive Clinical Practice (GCP) guidelines and regulatory requirements throughout all aspects of study conduct.

Job Requirements
Bachelor's degree in life sciences, pharmacy, or a related field.
Minimum 2 years of experience in clinical trial management and analysis, preferably in a pharmaceutical company setting.
Robust knowledge of GCP guidelines, regulatory requirements, and ICH guidelines.
Excellent analytical, problem-solving, and communication skills.
Ability to work independently and collaboratively as part of a team.
Proficiency in statistical software packages, such as SAS or R, is an asset.

📌 Centralized Study Analyst Bengaluru (India)
🏢 Naukri Healthcare Jobs
📍 India