Senior Pharmacovigilance Project Manager
Senior Pharmacovigilance Project Manager
Senior Pharmacovigilance Project Manager
Senior Pharmacovigilance Project Manager
ICON
Pharmazeutische Produkte, Arzneimittel
Bell
- Art der Anstellung: Vollzeit
- 73.000 € – 87.500 € (von XING geschätzt)
- Hybrid
- Zu den Ersten gehören
Senior Pharmacovigilance Project Manager
Über diesen Job
Senior Pharmacovigilance Project Manager - United States (Remote)
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We have an incredible opportunity for a Senior Pharmacovigilance Project Manager to join ICON’s Full-Service Pharmacovigilance & Safety Reporting group. The Senior PV PM manages assigned projects that may range from simple to complex or portfolio and span across business units or functional areas. They are providing valuable insight into how areas impact one another. The Senior PV PM will provide leadership to project teams comprised of cross-functional resources with a focus on delivering a completed high-quality project, within cost and on time.
Location: United States (Remote)
What you will be doing:
- Act as primary project manager for simple to complex project(s)/portfolio(s) and Pharmacovigilance vendor management
- Establish and continually manage complex projects/programs expectations while delegating tasks and responsibilities as appropriate
- Provide team leadership, mentoring and assessment feedback to project management team and functional leads to meet project deliverables/timelines with high quality
- Pharmacovigilance SME for Safety Standalones and full-service proposals
- Attend, participate in, and lead the project teams in bid defense processes
- Contribute to the development of practices, templates, and tools to promote learning and process improvements
- As required for complex projects/programs define success criteria and deliver appropriate and effective level communication, status reports and presentations to key stakeholders. Monitor, track and control outcomes to resolve issues, conflicts, dependencies and critical path deliverables
- Maintain professional development in order to keep up to date of technologies, methods and best practices
Your profile:
- 5+ years of pharmacovigilance experience, with a focus on quality, compliance, and risk management
- Safety reporting experience
- A solid understanding of global regulatory reporting rules
- Detail-oriented with a focus on accuracy, thoroughness, and consistency
- Excellent written and verbal communication skills
- Time management skills with the ability to prioritize efficiently
- Proactive mindset with strong critical thinking abilities to identify issues early and make sound, data-driven decisions
- Bachelor’s degree
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
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Unternehmens-Details
ICON
Pharmazeutische Produkte, Arzneimittel