Looking for a challenging role in clinical trial management? The position of Project Specialist I in Bangalore offers an excellent opportunity for individuals with a background in bioscience, computer science, or related fields. This role involves coordinating site and operational activities in clinical trials, ensuring that the trials run smoothly from start to finish. The job requires attention to detail, strong communication skills, and a dedication to maintaining high-quality service.
Essential Duties and Responsibilities
As a Project Specialist I, you will handle a variety of tasks to ensure the seamless execution of clinical studies:
- Study Start-Up and Documentation: Assist in preparing study materials and ensure timely completion of site qualifications by following up on outstanding documents.
- Site and Data Management: Coordinate trainings for site personnel, track and monitor study-related data, and resolve data discrepancies.
- Data Processing: Oversee the collection and maintenance of cardiovascular data, ensuring compliance with protocols.
- Project Administration: Support Project Managers by coordinating site start-up activities, tracking data, and participating in project meetings.
- Communication and Client Relations: Maintain communication with clinical sites, sponsors, and the study team, and provide timely updates on project progress.
- Reporting and Tracking: Generate and distribute reports, track project data, and identify trends that require action.
Qualifications and Skills
Experience:
- Familiarity with clinical trials, drug development, or clinical research is advantageous.
- Proficiency in software packages such as Microsoft Office, especially Excel, is required.
Skills:
- Strong interpersonal, leadership, and organizational skills.
- Ability to work independently and in teams with minimal supervision.
- Excellent attention to detail, goal-oriented, and adaptable to changing priorities.
