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Senior Marketed Product Safety Specialist

Employer
IQVIA
Location
London
Start date
4 Dec 2020
Closing date
3 Jan 2021

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Discipline
Clinical Research, Pharmacovigilance
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

RESPONSIBILITIES

  • Work closely with project teams to determine appropriate terms and conditions of safety agreements
  • Develop and prepare safety agreements
  • Prepare and maintain PSMFs
  •  Review PSMFs prepared by other specialists
  • Primary customer interface on large, complex projects, responsible for developing and maintaining customer relationships
  •  Provide input to project plans to accurately reflect services provided. Oversee finalization and distribution of safety agreements
  • Assist in the negotiation of safety agreement text using approved processes and templates.
  • Represent safety agreements team at customer meetings as required
  • Provide input into project budgets involving safety agreements.
  • Provide advice, support and guidance to other staff involved in preparing safety agreements.
  • Mentor and train team members
  • May assume the responsibilities of EU QPPV or deputy QPPV as outlined in Quintiles Work Instruction: CS_WI_LS0013 Lifecycle Safety-Qualified Persons for Pharmacovigilance (QPPV)
  • Perform all other duties as assigned

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

  • Excellent knowledge of Lifecycle Safety processes
  • Excellent attention to detail and accuracy and maintain consistently high quality standards.
  • Excellent written and verbal communication skills.
  • Ability to work effectively on multiple projects simultaneously. Organize own workload and effectively time manage competing priorities
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

  •  Bachelor's degree or educational equivalent in health science or other directly related field and a minimum of 3 years' experience of Lifecycle Safety (Pharmacovigilance, CEVA, Medical Information, safety Publishing, Risk Management etc) with project management experience or equivalent combination of education, training or experience.

PHYSICAL REQUIREMENTS

  • Extensive use of keyboard requiring repetitive motion of fingers.
  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech
  • Regular sitting for extended periods of time.
  •  May require occasional travel.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

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