
Principal Research Coordinator
2 semanas atrás
As a Clinical Research Associate, you will play a pivotal role in the success of our clinical trials. Your primary responsibilities include developing and maintaining strong relationships with study sites to ensure continuity and achievement throughout all phases of clinical research trials.
Key Responsibilities- Foster collaboration with study sites to guarantee seamless trial execution.
- Pursue site management and monitoring activities in compliance with ICH-GCP, sponsor SOPs, local laws, and regulations.
- Cultivate an in-depth understanding of study protocols and related procedures.
- Collaborate with other sponsor roles to achieve 'Site Ready' status.
You will also participate in site selection and validation activities, providing valuable insights. Conduct comprehensive site visits, including initiation, monitoring, and close-out visits, and document findings accurately and efficiently.
Main Requirements- A Bachelor's degree in life sciences, biology, or a related field is required.
- Previous experience as a Clinical Research Associate is highly beneficial.
- Fluency in Portuguese and advanced English (verbal and written) skills are essential.
- A thorough understanding of clinical research processes, phases of clinical trials, and current ICH Good Clinical Practice & country-specific clinical research laws and guidelines is necessary.
We seek a motivated and experienced professional to join our team in Sao Paulo, Brazil. If you possess a passion for clinical research and exceptional communication skills, we encourage you to apply for this exciting opportunity.
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