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Clinical Lead

ICON Public Limited Corporation

The Clinical Lead will supervisor all aspects of the Research Assistants workflow. Serves as the liaison for Research Assistant and works in conjunction with the...

The Clinical Lead will supervisor all aspects of the Research Assistants workflow. Serves as the liaison for Research Assistant and works in conjunction with the Principle Investigators(PIs), Project Manager(s) (PMs) and Clinical Research Coordinators (CRCs) to assign the appropriate clinical staff to execute the clinical trial. Ensures the quality of work of Research Assistants. Has frequent communication with a variety of individuals responsible for the execution of the clinical trial including, clinical research subjects, Principal InvestigatorI, Pharmacists, Study Managers, Clinical Research Coordinators, Clinical Operations Director, Clinical Manager and other staff as appropriate. * As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.

* As a Clinical Lead, the employee is expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.

* Travel (approximately 0%) domestic and/or international.

* Coordinate to ensure proper execution of clinical trial.

* Responsible for clarifying any clinical trial related issues to ensure proper execution of clinical trial.

* Apply all IEP CRU Standard Operating Procedures (SOP) applicable to job duties.

* Familiarize and understand protocol requirements.

* Participate in all internal and external clinical trial meetings, as appropriate.

* Ensure the collection of data and dataflow through the QC process (e.g. completion of internal queries).

* Participate in the QC execution and review of study documents (e.g. source documents, informed consents).

* Function as a Research Assistant as necessary to ensure adequate coverage of scheduled clinical trials.

* Give report to incoming Clinical Leads.

* Ensure compliance with all applicable regulations (e.g. OSHA, FDA, etc.).

* Follow any reasonable directives.

* To undertake other reasonable related duties as may be assigned from time to time.

Job posted: 2020-11-18

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