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Job Title		Senior Clinical research Physician

Job number		120143090

Posted		18/07/2008 (14:35)

Agency/Employer		ICON

Description		ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support clinical development - from compound selection to Phase I-IV clinical studies. ICON teams have successfully conducted over 1,900 development projects and over 2,300 consultancy engagements across all major therapeutic areas. ICON currently has over 5,200 employees, operating from 53 locations in 31 countries. ICON invites applications for the position of a (Senior) Clinical Research Physician to be based in our office in UK. 1. PURPOSE OF THE JOB: Provide the necessary support to ICON Project Teams on medical issues and input into ICON�s activities to ensure that projects of all phases (1-4) are conducted according to the highest ethical principles and in compliance with applicable legal and regulatory standards 2. JOB FUNCTIONS/RESPONSIBILITIES: Oversee safety issues of projects conducted by ICON which will include, but not be limited to, the following: Adverse event reporting to the sponsor Follow up of adverse events as necessary Communication of safety issues to the head of the department or designee Participate in the on-call system for providing 24/7 medical support Provide all necessary medical support functions as defined by project specific contractual obligations which will include, but not be limited to, the following: Medical information source Ongoing training for project teams in therapeutic areas as requested Review of study documentation (protocol, CRF. etc.) Contribute to investigator meeting presentations Ongoing safety review of individual patient laboratory reports generated by central laboratories CRF safety review Contribute any necessary medical input into integrated clinical and statistical reports Assist in making presentations to potential clients when appropriate Demonstrate a thorough understanding of ICON Standard Operating Procedures (SOPs) and ensure that all activities are conducted in accordance with current SOPs Demonstrate a thorough understanding of applicable regulatory standards in the country where clinical studies are to be conducted and ensure that all activities are conducted in compliance with current regulations Keep the person to whom the Clinical Research Physician reports informed of any issues within the department which require attention Line management of DSAs as appropriate 3. QUALIFICATIONS/EXPERIENCE REQUIRED: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions Medical degree and broad based post graduate experience Ability and willingness to travel on an as-need basis Ability to medically evaluate clinical data Good oral and written communication skills including proficiency in English Excellent presentation skills Preferably 2 years experience in a relevant clinical research role Good computer skills (MS: Outlook, Word, Excel)

Location		Eastleigh, Hampshire

Job type		Permanent

Contract length		N/A

Start date		ASAP



Contact name		Laura Hegan

Telephone		02380 688707

Ref no		SCRP

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