This is an exciting opportunity toworkwithin a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industrie
s.You will be responsible for coordinating and ensuring execution of all clinical study protocol activities within Good Clinical Practice (GCP) and the Food and Drug Administration (FDA) regulations and requirements, Sponsor expectations and ICON Development Solutions Standard Operating Procedures (SOPs) in the Omaha, NE location.
Overview of the Role
Communicate protocol requirements to clinical and laboratory staff.
Participate in the early planning phases of clinical study by providing assistance in the preparation of study proposal timelines, scheduling and other study requirements as appropriate.
Evaluate, coordinate, and ensure the completion of all protocol related tasks to include: design of procedural timeline; design of forms and source documents used in the clinical research process; maintain clinical study enrolment log; and assist Data Coordinators regarding CRFs and regulatory documents.
Coordinate with Study Manger to ensure appropriate timelines are being met as per contractual obligations.
Role Requirements / Skills / Experience Required
Previous research experience and Certified Clinical Research Coordinator (CCRC) preferred OR Bachelor’s degree with at least two (2) years medical experience.
Excellent written, oral communications, interpersonal and problem solving skills.
Detailed oriented with excellent organizational and prioritization skills.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
In addition you will have the opportunity to develop within your role and take on further responsibilities or develop your skill set within other related departments of ICON.
Following your application if you are successful you will be invited to an initial telephone interview with one of our dedicated recruiters who will be able to provide you with more details of this opportunity.
Clin - Pharmacology
18/Dec/12, 9:39:42 AM
ICON Clinical Research - 2 years ago
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