Key skills
Time Management
About this role
Role Overview
- Performing site selection, initiation, monitoring and close-out visits
- Supporting the development of a subject recruitment plan
- Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
- Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
- Collaborating with experts at study sites and with client representatives
Requirements
- University degree in scientific discipline or health care
- Experience in Pharma Industry, and/or Clinical Trials environment
- Very good computer skills including MS Office
- Excellent command of Spanish and English language
- Organizational, time management and problem-solving skills
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
- Flexibility to travel
- Driver’s license class B
Benefits
- Resources that promote your career growth
- Leaders that support flexible work schedules
- Programs to help you build your therapeutic knowledge
- Excellent working environment in a stabile, international, reputable company
- Mobile phone and attractive benefits package