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  Clinical Research Associates - Nationwide  
  Clinical Research Manager - San Diego and South San Francisco  
  Safety Monitor II - North Carolina  
  Clinical Research Physician-Hampshire, UK - South East  
  Clinical Project Managers (All levels) Belgium, Germany, UK - South East, UK - East Anglia, UK - Scotland (Central)  
       
       
    Clinical Research Physician-Hampshire

Salary: Negotiable
Location: United Kingdom, UK - South East
Reference: LD 12215

  Background:
Clinical Research International, a global l contract research organization requires a Clinical Research Physician within the Pharmacovigilance Department in Hampshire, in order to provide the necessary clinical support to the Company’s Project Teams on medical issues and input into company activities to ensure that clinical studies are conducted according to the highest ethical principles and in compliance with applicable legal and regulatory standards.
LOCATION AREA: UK South / UK South-East / Hampshire / M3 / Southampton region /  Winchester region
JOB ROLE: This role reports to the Medical Director / Associate Medical Director.

Principal responsibilities include:
Overseeing safety issues of clinical studies conducted by the Company which will
include, but not be limited to, the following:
a. Adverse event reporting to the sponsor
b. Follow up of adverse events as necessary
c. Communication of safety issues to Medical Affairs Manager (USA) and Medical Director (Europe)
d. Participate in the on-call safety monitoring procedure.
Providing all necessary medical support functions as defined by Company Senior
Management which will include, but not be limited to, the following:
a. Medical information source
b. Ongoing training for project teams in therapeutic areas as requested
c. Review of study documentation (protocol, CRF etc.)
d. Contribute to investigator meeting presentations
e. Ongoing safety review of individual patient laboratory reports generated by central laboratories (if requested by the Sponsor)
f. CRF safety review
g. Contribute any necessary clinical interpretation into integrated clinical and statistical reports
h. Assist senior management in making presentations to potential clients when appropriate.
Demonstrating a thorough understanding of Company Standard Operating Procedures (SOPs) and ensuring that all activities are conducted in accordance with current SOPs.
Demonstrating a thorough understanding of applicable regulatory standards in the country where clinical studies are to be conducted (e.g. Code of Federal Regulations for studies conducted in the USA) and ensure that all activities are conducted in compliance with current regulations.
Keeping the person to whom the Clinical Research Physician reports to informed of any issues within the department requires attention.
  QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
Medical degree and broad based post- graduate experience.
SAE experience is essential.
Ability and willingness to travel on an as-need basis.
Ability to review and evaluate clinical data.
SKILLS & PERSONAL ATTRIBUTES:
 Good oral and written communication skills (verbal and written).
Ability to liaise with Associate Medical Director and/or Medical Director.
BENEFITS OF THE ROLE: This is a wonderful opportunity for a physician to work in clinical research, in the knowledge that the contribution you make will be vital to the safety of global drug development. 

For applications or further information please email your CV Click Here....

 

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