Clinical Research Coordinator
We are now recruiting for a Clinical Research Coordinator (CRC)
for Rocky Mount site. This full time Permanent opportunity, reports
directly to the Clinical Operations Manager, with the primary aim;
to coordinate multiple studies according to the study protocol,
perform collection of clinical data points and to provide a
seamless, customer service to the patients attending site.
Our mission is to function as an Integrated Site Network, the
role of our Coordinators are paramount to achieving our
As a CRC Level 1, you will be responsible, day to day for the
- Performs study start-up duties including the production of a
recruitment tool, and progress notes, as well as phone screening
patients and identifying participants for trials on site
- Proactively develops and executes recruitment plans that meet
and exceed enrollment goals
- Completes training on Clinical Trial Management System and
maintains proper skills to update database, complete participant
reimbursement, capture referral source of participants, and create
calls lists to promote recruitment.
- Attends investigator meetings
- Performs technical requirements of the study protocol, i.e.,
lab work (phlebotomy and processing), blood pressure,
electrocardiograms, Holtor monitoring, pulmonary function testing,
allergy testing, urine/serum pregnancy testing, strep throat
screening, or any procedure necessary for the protocol as ordered
by the investigator or specified by a protocol
- Documents laboratory data and adverse reactions, presents this
information to an investigator in a timely manner, and immediately
notifies investigators, the Institutional Review Board and sponsor
of any serious adverse events
- Builds and maintains strong relationships with Investigators
and provides ongoing communication about trial status and
Successful applicants will have the following:
- Bachelor's life science degree, or relevant industry-field
- 1 years' work experience in clinical research or pharmaceutical
environment would be desirable
- High level of attention to detail
- Personable, able to build rapport with patients with ease
- Motivated about a career in clinical research
- Excellent planner, organized approach to work
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.