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Drug Safety Associate III

unlimited holidays - extra holidays - extra parental leave - long remote period allowed
Remote: 
Full Remote
Experience: 
Expert & Leadership (>10 years)
Work from: 

Offer summary

Qualifications:

Bachelor's degree in life science or healthcare, Minimum 10 years experience in pharmaceutical industry, Up-to-date knowledge of PV regulations.

Key responsabilities:

  • Establish departmental procedures and oversee training
  • Support pharmacovigilance activities and signal detection
  • Provide leadership in PV activities within department
  • Participate in safety evaluation group discussions
  • Collaborate in writing safety analysis reports
Katalyst HealthCares & Life Sciences logo
Katalyst HealthCares & Life Sciences Pharmaceuticals SME https://www.katalysthls.com/
51 - 200 Employees
See more Katalyst HealthCares & Life Sciences offers

Job description

Responsibilities:
  • Establishes and maintains departmental procedures; oversees training and continuous improvement.
  • Support DSP in pharmacovigilance activities including: signal detection and tracking activities, literature surveillance, oversight of medical review performed by outsourced vendor
  • Collaborate with DSP safety physicians with PV activities as assigned
  • Writing safety analysis reports
  • Oversight of medical review and aggregate report activities performed by outsourced vendors
  • Support clinical project teams for investigational products; provide project teams providing expertise in PV activities
  • Collaborate with Clinical Research and Development, medical Affairs, Regulatory Affairs
  • Provide Leadership in the development, implementation, and maintenance of robust procedures for PV activities within the DSP department
  • Participate on the Safety Evaluation Group with local and global drug safety colleagues to monitor and discuss safety signal evaluation topics
  • Contribute to the writing and compilation of PADERs, Annual reports and PSURs/PBRER.
  • Author and review department SOPs as needed.
  • Participate in Regulatory Inspections, external audits and investigator meetings
  • Drug safety representative on Purdue intradepartmental committee for review and approval of clinical trial protocol language and clinical study processes
  • Acts as a Subject Matter Expert in PV regulatory inspections and internal/external audits.
  • Collaborates with internal stakeholders and Purdue subsidiaries to establish and maintain the Corporate AE Policy.
  • Collaborate with Drug Safety Operations and Drug Safety Systems as needed, to ensure appropriate metrics per SOP.

Requirements:

  • Bachelor's degree (advanced degree preferred) in life science or healthcare (e.g. nursing, pharmacy)
  • Minimum 10 years of experience in a pharmaceutical/biopharmaceutical company
  • Minimum 7 years of Drug Safety experience
  • Up-to-date knowledge of US and international PV regulations and best practices
  • Thinks globally and considers present and future impacts when making recommendations
  • Experience with PV vendor and business partner oversight and contract/agreement management
  • Strong negotiation and problem-solving skills
  • Analytical skills and attention to detail
  • Accountability – takes ownership of deliverables

Required profile

Experience

Level of experience: Expert & Leadership (>10 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Analytical Thinking
  • Motivational Skills
  • Accountability
  • Detail Oriented

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