Clinical Study Professional

We are looking for a highly skilled and experienced Clinical Study Personnel 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 studies and a passion for delivering high-quality results.

Roles and Responsibility

• Conduct site monitoring visits to ensure compliance with study protocols and regulations.
• Collaborate with investigators, sponsors, and other stakeholders to resolve issues and ensure timely study completion.
• Develop and maintain accurate records of study data, including progress reports and final study reports.
• Provide training and support to site staff on study procedures and best practices.
• Ensure adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Participate in quality assurance activities to identify areas for improvement and implement changes.

Job Requirements

• Bachelor's degree in a related field such as life sciences or pharmacy.
• Proven experience in clinical studies, preferably in a pharmaceutical company setting.
• Strong knowledge of GCP guidelines, regulatory requirements, and ICH guidelines.
• Excellent communication and interpersonal skills, with the ability to work effectively with cross-functional teams.
• Ability to work independently and make sound decisions in fast-paced environments.
• Strong analytical and problem-solving skills, with attention to detail and accuracy.