Senior CRA
Job Details
Full Job Description
At ICON, it’s our people that set us apart. Our diverse teams
enable us to become a better partner to our customers and help us to
fulfil our mission to advance and improve patients’ lives.
Our
‘Own It’ culture is driven by four key values that bring us together
as individuals and set us apart as an organisation: Accountability &
Delivery, Collaboration, Partnership and Integrity. We want to be the
Clinical Research Organisation that delivers excellence to our clients
and to patients at every touch-point. In short, to be the partner of
choice in drug development.
That’s our vision. We’re driven by
it. And we need talented people who share it.
If you’re as driven
as we are, join us. You’ll be working in a dynamic and supportive
environment, with some of the brightest and the friendliest people in
the sector, and you’ll be helping shape an industry.
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
• 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
• At least 2 years of independent, on-site monitoring
experience in phase I-III trials 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
• 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
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.
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.
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 through the form below.
#LI-DK2
Are you a current ICON Employee? Please click here to apply: link
We
want to be the Clinical Research Organisation that drives more client
projects to market or accelerated decision than anyone else in the
industry. In short, to be the partner of choice in drug development.
That’s our vision. We’re driven by it. And we need talented people who
share it.
If you’re as driven as we are, join us. You’ll be
working in a great environment, with some of the brightest and the
friendliest people in the sector, and you’ll be helping shape an
industry.
Senior CRA
355 ICR South Africa - SAF
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