Clinical Research Study Coordinator - Optometry (Johns Creek, GA) at Pharmaceutical Research Associates, Inc. in Raleigh, North Carolina

Posted in Other 12 days ago.





Job Description:

Pharmaceutical Research Associates, Inc.

Clinical Research Study Coordinator - Optometry (Johns Creek, GA)

US-Remote


Job ID: 2021-84383
Type: US-Southeast
# of Openings: 1
Category: Clinical Trial Support

Alcon

Overview

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.



Responsibilities

What will you be doing?

Maintain the Investigator Site File (ISF):

  • Obtain essential documentation
  • Confirm all required documentation is complete prior to the Study Initiation Meeting (SIM)
  • Update ISF throughout the study as needed to meet regulatory and sponsor requirements
  • Confirm all documentation is complete at study close-out
  • Schedule and participate in the SIM
  • Prepare study specific documents (i.e. enrollment log, dispensing log, and subject final log) and subject information/supplies

Manage test article:

  • Verify receipt of test article
  • Prepare information and materials for subject dispensing
  • Maintain test article inventory throughout the study, re-ordering as needed
  • Perform test article reconciliation at study completion
  • Assist with subject scheduling

Participate in the execution of the study as delegated by the Principal Investigator on the delegation log:

  • Facilitate monitoring visits
  • Back-up for Clinical Research Scheduling Coordinator
  • Other duties as delegated by management



Qualifications

What do you need to have?

Qualifications:

  • Bachelor’s Degree or equivalent relevant experience
  • 2 years’ of experience with clinical research
  • Customer focused
  • Ability to multi-task and work in a fast paced environment
  • Team player




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.

PI149855814
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