Description
We are seeking a Clinical Research Associate to join our team.
As a Clinical Research Associate, you will be responsible for:
- 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, such as 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
To qualify for this role, you will need:
- A university degree in a scientific discipline or healthcare
- 2-4 years of independent on-site monitoring experience
- Very good computer skills, including MS Office
- Excellent command of Portuguese and English languages
- 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
In return, you can expect:
- Resources that promote your career growth
- Leaders that support flexible work schedules
- Programs to help you build your therapeutic knowledge
- An excellent working environment in a stable, international, reputable company
- A company car, mobile phone, and attractive benefits package