FSP Sr CRA Level I - São Paulo

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global team, you'll have the opportunity to perform and coordinate all aspects of the clinical m ...

Monitors investigator sites with a risk-based monitoring approach applies root cause analysis RCA critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. · ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2, · 700 clinical trials across 100+ countries in the last 5 years. · As part of our global team you'll have · the opportunity to perform and coordinate all aspects of the clini ...

The CRA (Level II) will be responsible for monitoring investigator sites with a risk-based approach, applying root cause analysis and problem-solving skills to identify site processes failure and corrective/preventive actions. · ...

The CRA (Clinical Research Associate) will monitor investigator sites with a risk-based monitoring approach. They will apply root cause analysis to identify site processes failure and corrective/preventive actions to bring the site into compliance. · They will ensure data accurac ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, · spanning 2,700 clinical trials across 100+ countries in the last 5 years. · Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation. · ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning · 2, · 700 clinical trials across · 100+ countries in the last five years. · J · Frequent drives to site locations. · )Frequent travel generally sixty-eight percent but more f ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs. As a Senior Clinical Research Associate (Level I), you'll conduct remote or on-site visits to assess protocol and regulatory compliance. You will manage procedures and guidelines from d ...

We have successfully supported the top pharmaceutical companies and more than biotechs spanning clinical trials across countries in years.Join our global team and perform coordinate different aspects of clinical monitoring site management process. · As Clinical Research Associate ...

Monitor investigator sites with a risk-based monitoring approach: apply root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. · ...

Work Schedule · Standard (Mon-Fri) · Environmental Conditions · Office · Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site · processes failure and corrective/preventi ...

Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. · ...

Work Schedule · Standard (Mon-Fri) · Environmental Conditions · Office · Join Us as a Senior Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation · We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spa ...

+Job summary · We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. · +Qualifications · Bachelor's degree in a life sciences related field or a Registered Nursing c ...

Work as a Sr CRA Level II with experience in Immunotherapy and Cell. · ...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. · Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and SOPs to assess the safety and efficacy of investigational pr ...

We are seeking a Clinical Research Associate III to join our team in Sao Paulo. The successful candidate will be responsible for conducting site visits, monitoring data quality and patient safety, and providing protocol and related study training to assigned clinical study sites. ...

We are seeking a Clinical Research Associate to join our team in Sao Paulo or Rio de Janeiro. As a CRA, you will be responsible for conducting site monitoring visits, building relationships with investigative sites, and ensuring quality and data integrity. · ...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. · ...

+As a Clinical Research Associate at Parexel, you'll be more than a monitor—you'll be a strategic partner and the primary point of contact for clinical sites throughout the entire trial lifecycle. · You'll own site performance, build meaningful relationships, · solve complex chal ...