FSP CRA Level I

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 ...

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. · ...

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 ...

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. · As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, · interpreting complex medical data, · and contributing to the a ...

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. · Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation. · ...

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 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 ...

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. · ...

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 ...

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 ...

+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 ...

+This job 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 · CRA must have adequate oncology monitoring experience. In addition, sufficient breast CA experience is strongly advised in order for the CRA to be successful on this complex metastatic breast CA study which ...

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 ...

Work Schedule · Standard (Mon-Fri)Environmental Conditions · OfficeJob Description · CRA must have adequate oncology monitoring experience. In addition, sufficient breast CA experience is strongly advised in order for the CRA to be successful on this complex metastatic breast CA ...

This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. · Work Schedule · Standard (Mon-Fri) · Environmental Conditions · Office · Job D ...

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 ...