Location - San Antonio, Texas.
Full Time Night Shift
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 industries.The Clinical Supervisor will supervise all aspects of clinician workflow as directed by the Principal Investigator (PI), Medical Director (MD) and Senior Clinical Manager. Serves as the liaison for Research Clinicians and works in conjunction with the (PIs), Project Manager(s) (PMs) and Clinical Research Coordinator (CRC) to assign the appropriate clinical staff to execute the clinical trial(s). Ensures the quality of work of Research Clinicians. Has frequent communication with a variety of individuals responsible for the execution of the clinical trial(s) including, clinical research subjects, PI, Pharmacists and other staff as appropriate
Overview of the Role
Coordinate with (PI), (CRC) and (PM) to ensure proper execution of clinical trial.
Responsible for clarifying any clinical trial related issues with PI, CRC and PM to ensure proper execution of clinical trial
Ensure the collection of data and dataflow through the quality control process (e.g. completion of internal queries).
Participate in the quality control execution and review of study documents (e.g. source documents, informed consents).
Role Requirements / Skills / Experience Required
Licensed Registered Nurse, Licensed Vocational Nurse or Licensed Paramedic is required
A minimum of one year experience in clinical research or related field.
A minimum of one year of management / leadership /assistant supervisor experience is preferred
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
06/Mar/13, 4:13:20 PM
ICON Clinical Research - 22 months ago
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Contract research organization (CRO) ICON is not iconic yet, but it would like to be. By the time a new drug hits the market, it has passed...