We are looking for a highly motivated and detail-oriented Clinical Project Associate to join our team at Ruputed Pharmaceutical Company. The ideal candidate will have a strong background in the pharmaceutical industry and excellent project management skills.
Roles and Responsibility
Coordinate clinical trial activities, including site initiation, monitoring, and close-out visits.
Develop and maintain study timelines, budgets, and resource allocation plans.
Collaborate with cross-functional teams, including data management, biostatistics, and medical writing.
Ensure compliance with regulatory requirements and company policies.
Manage and resolve issues related to study start-up, protocol deviations, or patient safety concerns.
Prepare and present reports on study progress, risks, and mitigation strategies.
Job Requirements
Bachelor's degree in life sciences, pharmacy, or a related field.
Proven experience in clinical trials, preferably in a pharmaceutical company setting.
Robust knowledge of Positive Clinical Practice (GCP) principles and regulations.
Excellent communication, organizational, and problem-solving skills.
Ability to work effectively in a fast-paced workplace and prioritize multiple tasks.
Proficiency in Microsoft Office and other relevant software applications.