Job Description

Our client a prestigious CRO is looking for a drug safety monitor to become familiar with all applicable regulations and company SOPs relevant to safety monitoring, adverse events and serious adverse event reporting in clinical studies and to become proficient and self-sufficient in conducting all procedures in relation to safety monitoring.

JOB FUNCTIONS/RESPONSIBILITIES:

• Familiarity with company Clinical Research SOPs, Study Specific Adverse Event Reporting SOPS, and appropriate regulations.
• Maintain adverse event database/ tracking system and paper files.
• Safety review of clinical data.
• Be cost effective.
• Keep the person to whom the Drug Safety Monitor reports informed of any safety related issues within the department which require attention.

QUALIFICATIONS/EXPERIENCE REQUIRED:

• Nursing/ paramedical background (entry level).
• Computer literacy.
• Good oral and written communication skills.

JOB GENERAL DETAILS:
£18 - 22K

Qualifications/Skills Required

• Nursing/ paramedical background (entry level).
• Computer literacy.
• Good oral and written communication skills.