Drug Safety Associate

We are looking for highly dynamic and professionally sound applicants for a progressive role in Pharmacovigilance, Safety Reporting and Strategic Regulatory team

Your responsibility includes:
1.The role involves the following tasks -Complete all departmental project activities accurately in accordance with ICON SOPs, Study Specific Procedures, regulatory requirements, and Sponsors processes
2.Review and process serious adverse events, spontaneously reported adverse reactions and/or other medically related information per assigned tasks and study specific procedures
3.Provide input and review relevant safety tracking systems for accuracy and quality and assist with maintaining project files
4. Attend project team meetings and teleconferences as required
*Serve a source for investigational sites and ICON personnel on safety-related issues
*Assist with training/mentoring newly hired DSA staff, as requested
*Assist with identifying out of scope activities in conjunction with the MSS Functional Lead
*Assist with generation of study specific procedures
5.Liaise with Sponsor and attend Sponsor meetings, as required
*Perform safety review of clinical and diagnostic data
* Liaise with investigational site, reporter, and/or Sponsor as necessary regarding safety issues
6. Your Good command of English (oral and written) is much essential .

Your benefits of working in icon
ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a phenomenal career.

ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.