Accessability Links
Cookies on our website
By continuing to use this website we will assume you are happy to receive cookies as outlined in our cookie policy
Accept Policy

Senior Clinical Research Associate - All US locations

US-Pennsylvania-North Wales; US-California-Los Angeles; US-Texas-Dallas; US-California-San Francisco; US-Texas-Houston; US-North
Permanent
Reference: 053610
This vacancy has now expired.
Description
As a global provider of drug development solutions, our work is serious business. But that doesn’t mean you can’t have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?
 
We are looking for passionate, resilient, and inspiring individuals to join our team. As a Senior Clinical Research Associate at ICON, you will work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP. We pride ourselves on our supportive company culture, where we work as one team to achieve industry-leading results.
 
The role
  • Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
  • Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
  • Managing sponsor generated queries
  • Taking responsibility for study cost effectiveness
  • Preparation and review of study documentation and feasibility studies for new proposals
  • Potential to assist in training and mentoring fellow CRAs
What you need
  • University degree in life science or related discipline OR RN/LPN with 4 years related experience
  • Minimum 12 months of onsite monitoring experience
  • Previous monitoring experience in medium sized studies, including study start-up and close-out
  • Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
  • Excellent written and verbal communication
  • Ability to work to tight deadlines
  • Availability to travel at least 65-70% of the time
Why join us?
Ongoing development is vital to us, and as a CRA you will have the opportunity to progress your career, with the potential to move into other related areas to enhance your skill set. Our benefits package is competitive, our scope is international and we genuinely care about our people and their success. Working for ICON you will be provided with a comprehensive benefits package including premium salary, bonus, 401K with employer match, generous PTO, paid holidays, company cell phone, FSA and college savings plan.
 
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
 
#LI-JS1
 
Similar jobs
(A) Account Executive (Clinical-West Coast, US)

US-California-San Francisco; US-North Carolina-Raleigh

Permanent

View Job Shortlist

(Senior) Principal Scientist, Patient Centered Outcomes

US-Maryland-Gaithersburg; US-North Carolina-Raleigh

Permanent

View Job Shortlist

Account Manager C&SR

US-North Carolina-Raleigh, ICR

Permanent

View Job Shortlist

Author Relations Project Manager, Clinical Outcome Assessments

US-North Carolina-Raleigh, ICR

Permanent

View Job Shortlist

Biostatistician, Real World Evidence

US-Kentucky-Lexington; US-New York-New York City; US-California-San Diego

Permanent

View Job Shortlist

 

Back to Top