Sanofi

Global Periodic Reporting Lead

Sanofi$178K — $257K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of international pharmacovigilance experience for marketed drugs and clinical development projects
  • Proven collaboration skills across multidisciplinary teams
  • Experience in compiling and drafting Periodic Safety Reports (PSRs) and safety reports
  • Strong analytical skills with a solid grasp of clinical safety processes
  • Knowledge of global regulatory frameworks and ICH guidelines related to PSRs
  • Demonstrated leadership abilities, including team development and problem-solving
  • Effective communication and computer literacy skills.

Responsibilities

  • Ensure compliance and control in Periodic Safety Report (PSR) authoring and vendor oversight
  • Lead and mentor the Periodic Report Expert (PRE) Team in alignment with organizational goals
  • Develop outsourcing strategies for PSR authoring based on business priorities
  • Oversee annual regulatory planning for PSRs across the full company portfolio
  • Manage the PSR Planning Team, focusing on resource allocation and training needs
  • Act as system owner for PSUR webpage repository and tracking tools
  • Identify and drive efficiency improvements in PSR processes.

Benefits

  • Supportive, future-oriented team environment
  • Opportunities for career growth through promotions and lateral moves
  • Comprehensive rewards package recognizing employee contributions
  • Extensive health and wellbeing benefits including healthcare and wellness programs
  • At least 14 weeks of gender-neutral parental leave.
Full Job Description
Job title: Global Periodic Reporting lead

Location: Cambridge, MA / Morristown, NJ / Swiftwater, PA

About the Job

As Global Periodic Reporting Lead within our Pharmacovigilance team, you will ensure and develop robust , compliant, and controlled processes for Periodic Safety Report (PSR) authoring and vendor oversight. You will lead the Periodic Report Expert (PRE) Team through coaching and mentorship while managing the annual worldwide regulatory planning of PSRs for the entire company portfolio. You will develop and execute outsourcing strategies, uphold regulatory compliance, and drive process improvements to leverage efficiencies. Ready to get started?

Main Responsibilities:
  • Ensure and develop robust , compliant, and controlled processes for Periodic Safety Report (PSR) authoring and vendor oversight while upholding regulatory compliance expectation
  • Lead the Periodic Report Expert (PRE) Team through coaching, mentorship, and development planning according to individual and organizational priorities
  • Develop and execute outsourcing strategies for PSR authoring according to business criticality and resourcing needs
  • Establish and maintain the annual worldwide regulatory planning of PSRs for the entire company portfolio (clinical and postmarketing)
  • Manage PSR Planning Team with regard to PSR planning activities, resource allocation, and training needs
  • Serve as system owner for the PSUR Web page Repository and tracking tool database
  • Identify, implement, and support process improvements to leverage efficiencies and drive continuous improvement


About You

Experience:
  • Experience in international pharmacovigilance for marketed drugs and/or projects under clinical development
  • Proven track record in transversal collaboration
  • Experience compiling and drafting PSRs and safety reports

Technical and Soft Skills:
  • Excellent technical, clinical and critical analytical skills with keen understanding of clinical safety processes and analysis
  • Strong understanding of global regulatory framework governing PSRs and worldwide pre and post marketing safety reporting regulations and ICH guidelines
  • Leadership skills including team motivation, problem-solving, initiative-taking, and strong negotiation skills
  • Process improvement experience (LEAN, Continuous Improvement) and project management of multifactorial activities with successful prioritization
  • Excellent written and oral communication skills and computer literacy

Education:
  • Bachelor's degree in health science or related field

Languages:
  • Fluent English (written and spoken)


Why Choose Us?
  • Bring the miracles of science to life alongside a supportive, future-focused team.
  • Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
  • Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
  • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.


The salary range for this position is:
$178,500.00 - $257,833.33

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.

About Sanofi

Sanofi is a global pharmaceutical company that specializes in the research, development, and manufacturing of prescription drugs and vaccines. The company operates in over 170 countries and has a diverse portfolio of products that includes treatments for diabetes, cancer, cardiovascular disease, and rare diseases. Sanofi is committed to improving global health and has a strong focus on innovation and sustainability. The company has received numerous awards for its research and development efforts and is recognized as a leader in the pharmaceutical industry.
Learn more about Sanofi
Market Cap
$121.6 billion
Industry
Net Income
$12.3 billion
Founded
1990
5 Year Trend
+2.5%
Revenue
$37.3 billion
NASDAQ

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