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Senior CRA and CRA II - home based in Finland

ICON Public Limited Corporation

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

As a Senior 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:

* 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

* Assist in training and mentoring less expert CRA's and lead CRA's working on international projects

What you need

* 2.5 years + of monitoring experience in phase I-III trials as a CRA (18 months + for CRA II)

* Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data

* You will possess excellent written and verbal communication in English

* Ability to produce accurate work to tight deadlines within a pressurized environment

* You will be asked to travel at least 60% of the time (domestic -fly and drive) and should possess a valid driving license

Benefits of Working in ICON:

Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.

We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.

But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

Job posted: 2021-08-05

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