Location: Leeds, United Kingdom
Closing Date: 12 Nov 16
Salary (£): Competitive
We are looking for candidates with a minimum of 2 years of Clinical Monitoring Experience.
General On-Site Monitoring Responsibilities:
o Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
o Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
o Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review. Monitor data for missing or implausible data
o Ensure the resources of the Sponsor and Covance are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Covance travel policy
o University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure),
o a minimum of 2 years of Clinical Monitoring Experience
Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.
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