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Experience Level
Senior
Qualifications
The ideal candidate will possess a strong background in clinical research with proven experience in managing clinical trials. Key responsibilities include: Independently manage all aspects of study site operations to ensure patient safety and data quality. Provide guidance on audit readiness and assist in preparation for audits. Develop and maintain trial management tools and status reports. Oversee site start-up procedures, including feasibility assessments and investigator recruitment.
About the job
Join our expanding team at pfm as a Senior Clinical Research Associate and play a crucial role in advancing clinical studies across Brazil. This remote position allows you to leverage your extensive experience in managing complex clinical trials while ensuring adherence to the highest standards of patient safety and data integrity.
As a Senior CRA, you will be responsible for overseeing the start-up and implementation of clinical studies, conducting on-site monitoring, and providing ongoing site management. You will collaborate closely with Clinical Trial Managers and Project Managers to support trial activities, with an emphasis on mentoring and training junior staff members.
About pfm
pfm is a leader in clinical research services, dedicated to advancing medical science and improving patient outcomes. With a focus on innovation and excellence, we are committed to providing our clients with the highest quality research services across Latin America.
Clicking Apply Now takes you to AutoApply where you can tailor your resume and apply.
Unlock Your Potential
Generate Job-Optimized Resume
One Click And Our AI Optimizes Your Resume to Match The Job Description.
Is Your Resume Optimized For This Role?
Find Out If You're Highlighting The Right Skills And Fix What's Missing
Experience Level
Senior
Qualifications
The ideal candidate will possess a strong background in clinical research with proven experience in managing clinical trials. Key responsibilities include: Independently manage all aspects of study site operations to ensure patient safety and data quality. Provide guidance on audit readiness and assist in preparation for audits. Develop and maintain trial management tools and status reports. Oversee site start-up procedures, including feasibility assessments and investigator recruitment.
About the job
Join our expanding team at pfm as a Senior Clinical Research Associate and play a crucial role in advancing clinical studies across Brazil. This remote position allows you to leverage your extensive experience in managing complex clinical trials while ensuring adherence to the highest standards of patient safety and data integrity.
As a Senior CRA, you will be responsible for overseeing the start-up and implementation of clinical studies, conducting on-site monitoring, and providing ongoing site management. You will collaborate closely with Clinical Trial Managers and Project Managers to support trial activities, with an emphasis on mentoring and training junior staff members.
About pfm
pfm is a leader in clinical research services, dedicated to advancing medical science and improving patient outcomes. With a focus on innovation and excellence, we are committed to providing our clients with the highest quality research services across Latin America.