Safety Project Manager

• Bachelor's Degree Health science or other directly related field or equivalent experience
• 4 to 6 years' clinical research experience in a Contract Research Organization or Pharmaceutical company combining 4 years of Lifecycle Safety (Pharmacovigilance, CEVA, Medical Information, Safety Publishing, Risk Management etc.) and 2 years' project management experience
• Strong knowledge of applicable global, regional and local clinical research regulatory requirement; i.e.Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines, IQVIA Standard Operating Procedures.
• Working knowledge of Lifecycle Safety service lines; willingness to increase knowledge across Lifecycle Safety service lines and develop new skills.
• Excellent team management and leadership skills, conflict management.
• Strong project management; planning and organizational skills.
• Effective verbal and written communication skills including ability to network and lead teleconferences.
• Effective collaborative, organizational and delegation skills.
• Ability to establish and maintain effective working relationships with coworkers, managers and customers.
• Ability to deliver on multiple projects and manage competing priorities.
• Effective business focus, marketing, sales skills.
• Proven strong presentation; report writing skills and customer focus skills.
• Ability to achieve results through communication, facilitation, negotiations in a matrix service delivery environment with shared accountabilities.
• Independent judgment, negotiating, decision-making, and problem solving skills.
• Effective business acumen and financial analytical skills, tactical planning, budgeting.
• Customer focused with effective relationship building skills.
• Effective motivating, influencing and conflict resolution skills.
• IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
• We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
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IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

• IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
• All information and credentials submitted in your application must be truthful and complete.
• Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
• We appreciate your honesty and professionalism.
• location
• and/or schedule (full or part-time)

Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.