Global Safety Officer, Rare
Company: Sanofi
Location: Morristown
Posted on: April 25, 2025
Job Description:
Job title: Global Safety Officer, Rare
Location: Bridgewater, NJ
About the Job
Are you ready to shape the future of medicine? The race is on to
speed up drug discovery and development to find answers for
patients and their families. Your skills could be critical in
helping our teams accelerate progress.
We are an innovative global healthcare company with one purpose: to
chase the miracles of science to improve people's lives. We're also
a company where you can flourish and grow your career, with
countless opportunities to explore, make connections with people,
and stretch the limits of what you thought was possible. Ready to
get started?
Main Responsibilities:
- Provide pharmacovigilance (PV) and risk management expertise to
internal and external customers
- Safety expert for product; must have an attitude of continuous
learning and understand the product attributes and science
- Maintain knowledge of product, product environment, and recent
literature
- Maintain expertise in drug safety and PV, and understanding of
international safety regulations and guidelines
- Lead cross functional Safety Management Teams (SMTs), Global PV
(GPV) teams and internal Safety Analysis Teams (SATs)
- Communicate with and represent PV position within
project/product teams, with external partners, key opinion leaders,
Health Authorities, and during internal and external
negotiations
- Provide strategic and proactive safety input into development
plans
- Support due diligence activities and PV agreements
Impact:
- Ongoing assessment of the safety status of the product
- Review, preparation, contribution and/or approval of clinical
development documents including clinical development plans, SAPs,
study protocols, investigator brochures, data monitoring plans,
study reports, integrated summary of safety, summary of clinical
safety, and labeling
- Review, preparation, and/or contribution to questions/requests
from health authorities, ethics committees/ IRBs, external
partners
- Management of product safety alerts
- Ensuring the GPV's position is well articulated to and
understood by its internal and external stakeholders
- Continued visibility and establishment of the credibility of
GSO role/function and consequently GPV
Signal Detection and Assessment:
- Responsible for overseeing from multiple contributors signal
detection and analysis
- Collaborate with Center of Excellence for Signal Detection and
Data Mining and the Safety Epidemiology group
- Identify and implement proactive safety analysis strategies to
further define the safety as well as Benefit Risk profile.
- Lead the review of aggregate safety data and related activities
as well as coordinate safety surveillance activities Qualifications
Knowledge and Skills
About You
- Excellent clinical judgment
- Articulate and clearly understood in telephone
communications
- Capability to synthesize and critically analyze data from
multiple sources supported by sound clinical reasoning
- Ability to communicate complex clinical issues and analysis
orally and in writing
- Able to develop and document sound risk assessment
- Demonstrates initiative and capacity to work under pressure and
with a good sense of Prioritization of business critical
deliverables
- Demonstrates leadership within cross-functional team
environment
- Excellent teamwork and interpersonal skills are
required
- Fluency in English (written and spoken). Formal Education And
Experience Required
- M.D. Degree or equivalent. (i.e. MB.BS or DO)
- MD, Board Certified/Board eligible, or international
equivalent, is preferred
- M.D., minimum 2-3 years' of unsupervised clinical practice (not
residency) and a minimum of 3 years in total experience in
international or large market pharmacovigilance, or at least 4
years of clinical development experience
- Exceptionally, candidates may be considered if they have proven
excellence in a similar prior position, even if they have less than
3 years international PV experience.
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.
BRIDGEWATER, NJ ONLY - Office Location Update
Sanofi's Bridgewater, NJ office is scheduled to relocate to
Morristown, NJ on or around March 24, 2025 and this role will then
be based in Morristown, NJ.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and
Affirmative Action employers committed to a culturally diverse
workforce. All qualified applicants will receive consideration for
employment without regard to race; color; creed; religion; national
origin; age; ancestry; nationality; marital, domestic partnership
or civil union status; sex, gender, gender identity or expression;
affectional or sexual orientation; disability; veteran or military
status or liability for military status; domestic violence victim
status; atypical cellular or blood trait; genetic information
(including the refusal to submit to genetic testing) or any other
characteristic protected by law.
#GD-SG
#LI-GZ
#LI-Onsite
#vhd
All compensation will be determined commensurate with demonstrated
experience. Employees may be eligible to participate in Company
employee benefit programs, and additional benefits information can
be found here.PandoLogic. Keywords: Security Guard, Location:
Morristown, NJ - 07963 , PL: 597218988
Keywords: Sanofi, Waterbury , Global Safety Officer, Rare, Other , Morristown, Connecticut
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