Senior CRA - £5,000 sign on bonus available

Senior CRA

At ICON, it's our people that set us apart.

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?

As a Clinical Research Associate at ICON, you'll 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 amazing company culture, where we work as one team to achieve industry-leading results.

The RoleWorking independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentationSubmission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requestedParticipate in preparing and reviewing study documentation and feasibility studies for new proposals as requiredBalancing sponsor generated queries efficiently and responsible for study cost-effectivenessDependent on level of experience you may assist in training and mentoring less expert CRA's and/or lead CRA's working on international projects

What you need18 months+ of monitoring experience in phase I-III trials as a CRA IIKnowledge of ICG GCP guidelines and expertise to review and evaluate medical dataOncology experienceYou will possess excellent written and verbal communication in EnglishAbility to produce accurate work to tight deadlines within a pressurized environment