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- Delivering training of investigators, site staff and project teams
- Work with complex studies in Infectious Diseases and Oncology
- Perform CRF review, source document verification and query resolution
- Site communication and management
- Site identification process
- Contact for clinical investigators, vendors and support services in regard to study progress
- Participate in feasibility research
- Preparation and delivering of presentations at Investigator's Meetings
- Preparation for and attendance at company's audits; resolution of audit findings
- Support to Regulatory Affairs in procurement of site regulatory documents
- Maintenance of study-specific automated tracking systems
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Full working proficiency in Portuguese and English
- Independent on-site monitoring experience in Brazil
- Experience in all types of monitoring visits in Phase II and/or III
- Availability to travel
- Experience in Oncology or Infectious Diseases is a plus
- Proficiency in MS Office applications
- Ability to plan and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
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Senior Clinical Research Associate - São Paulo, Brasil - PSI
Descrição
Job Description
Home-based in Brazil
Only CV's in English will be considered
We are looking for an experienced CRA ready to train and coordinate junior CRAs on site. Here you will have the opportunity to develop yourself as a trainer, mentor and leader. We are committed to develop our employees in their careers by providing tailored courses and mentoring.
Responsibilities will include:
Qualifications
Additional Information
Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with a rapid growing company that puts its people first.
Usuários da profissão Senior Clinical Research Associate em São Paulo
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André Luigi Cleto
Clinical Research Assistant