CRA I
- Company
- ICON Clinical Research
- Location
- Germany,köln
- Salary
- Competitive
- Posted
- 18 Feb 2021
- Closes
- 20 Mar 2021
- Ref
- JR064243
- Discipline
- Clinical Research
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
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 Role
What you need
The Role
- Working independently and actively to coordinate activities to set up and monitor a study, completing accurate study status reports and maintaining study documentation
- Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
- Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
- Balancing sponsor generated queries efficiently and responsible for study cost-effectiveness
- Dependent 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 need
- +1 years of monitoring experience as a CRA
- Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
- You will possess excellent written and verbal communication in English and local language (German)
- Ability to produce accurate work to tight deadlines within a pressurized environment
- You will be asked to travel at least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license
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