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.
Our Clinical Delivery team is world class and as a Clinical Research Associate
within our EMEA Clinical Delivery team you will have the opportunity to work
within a structure that is built to support growth and development of our
team. We ensure that we leverage our top talent to enable the expansion of
skill sets and advanced training as much as possible.
Our Clinical Research Associates are ultimately responsible for the successful
management of investigator sites throughout the trial lifecycle. You will have
the opportunity to work on a range of therapeutic areas and supported on your
ICON journey by both a dedicated functional manager and also the cutting edge
and user friendly technology that we have here at ICON.
Key Responsibilities Include
* Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out.
* Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan.
* Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
* Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues.
* Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines
You will be operating as a key part of a global study team and plays a
fundamental role in our clients’ drug development processes.
To Enable Success In This Position You Will Have
Here at ICON we want our employees to succeed and ensure that they are set up
for this success through constant training, development and support.
* Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.
* A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
* You will be educated to degree level, have equivalent experience or be a licensed healthcare professional.
ICON is an equal opportunity and inclusive employer and is committed to
providing a workplace free of discrimination and harassment. All qualified
applicants will receive equal consideration for employment without regard to
race, color, religion, sex, sexual orientation, gender identity, national
origin, disability or protected veteran status.
Benefits Of Working In ICON
Our success depends on the knowledge, capabilities and quality of our people.
That’s why we are committed to developing our employees in a continuous
learning culture – one where we challenge you with engaging work and where
every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive
total reward package that comprises, not only an excellent level of base pay,
but also a wide range of variable pay and recognition programs. In addition,
our best in class employee benefits, supportive policies and wellbeing
initiatives are tailored to support you and your family at all stages of your
career – both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer
and is committed to providing a workplace free of discrimination and
harassment. All qualified applicants will receive equal consideration for
employment without regard to race, color, religion, sex, sexual orientation,
gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable
accommodation for any part of the application process, or in order to perform
the essential functions of a position, please let us know.
