Drug Safety Associate
About the role
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- Complete all departmental project activities accurately in accordance with ICON SOPs, Project Specific Procedures, regulatory requirements, and Sponsors processes.
- Review and process safety events (pre-marketing, post-marketing, device and drug) and/or other medically related information per assigned tasks and project specific procedures.
- Provide input and review relevant safety tracking systems for accuracy and quality and assist with maintaining project files.
- Perform safety review of clinical and diagnostic data as part of case processing.
- Generation of project specific procedures
- Act as Pharmacovigilance lead for regional projects, or assist as needed with global projects
- Support creation of post-marketing safety activities, such as PSMF, RMP and PBRER.
- Support QPPV as required.
- Support development of clinical trial activities such as DSURs, 6-monthly line listings, by liaising with other ICON departments and/or other Sponsor vendors
- Liaise with investigational site, reporter, and/or Sponsor as necessary regarding safety issues.
- Liaise with ICON Medical Monitor, project manager, and other departments, as appropriate.
- Assist with identifying out of scope activities in conjunction with the PV Project lead (as applicable).
- Actively identify out of scope activities
- Attend project team and Sponsor meetings (including Investigator meetings) and teleconferences as required.
- Train/Mentor Drug Safety Associate staff
- Participation in interdepartmental activities (e.g. quality control processes, quality assurance (audits), miscellaneous project activities)
- Assist management with weekly and monthly project status reports including quality review findings and metrics
- Assist with development and conduct of safety presentation for start-up meetings, Investigator meetings and other meetings
- Perform other activities as identified and requested by management.
- You will possess a minimum of 2 year pharmacovigilance experience or other equivalent clinical or pharmaceutical experience along with a RN, Bachelor’s in Nursing, , or RPH or PharmD, or equivalent experience as a licensed healthcare professional.
- Knowledge of medical terminology and coding systems
- Basic computer skills (Microsoft Word, Excel, Outlook, Access)
- Good communication skills
- Detail oriented
- Fluent in written and verbal English
- Work effectively within a team environment
Application process
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