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 solid 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 Good 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.
- Strong 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)
🏢 Naukri Healthcare Jobs
📍 Bengaluru