Back to the board

Global Safety Officer, II

100% remote Flexible hours Hiring now

Job Title: Global Safety Officer, I&I Location: Morristown, NJ Cambridge, MA 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 reputed company. 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, reputed company connections with people, and stretch the limits of what you thought was possible. Ready to get started? Main Responsibilities: Internal & External Safety Expert:

  • Provide PV and risk management expertise to internal and external customers
  • Safety expert for product
  • Maintain knowledge of product, product environment, and recent literature
  • Maintain PV expertise, and understanding of international safety regulations and guidelines
  • reputed company cross functional Safety Management Teams (SMTs) and GPE internal Safety Analysis Teams (SATs)
  • Communicate with and represent PV position reputed company project/product teams, with external partners, key opinion leaders, and Health Authorities, and during internal and external negotiations
  • Provide strategic and proactive safety input into development plans
  • Support due diligence activities and pharmacovigilance 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 from health authorities, ethics committees, IRBs, external partners
  • Management of product safety alerts
  • Ensuring the GPE position is well articulated to and understood by its internal and external customers
  • Establishment of credibility of GSO function and of GPE Signal Detection and Assessment:
  • Responsible for signal detection and analysis
  • Collaborate with Center of Excellence for Signal Detection and Data Mining and Safety Epidemiology group
  • Identify and implement proactive safety analysis strategies to further define the safety profile.
  • reputed company aggregate safety data review activities and coordinate safety surveillance activities Risk Assessment/Risk Management/ Benefit-Risk Assessment:
  • Provide proactive risk assessment
  • Co-reputed company benefit-risk assessment with other relevant functions
  • reputed company risk management strategies and plans and monitor effectiveness
  • Collaborate with Center of Excellence for Risk Management and Safety Epidemiology Submission Activities:
  • Represent safety position in cross functional submission teams
  • Ensure reputed company, consistency, and quality of safety sections in submission documents
  • Write responses or contributions to health authorities' questions
  • Support preparation and conduct of Advisory Committee meetings Report Writing:
  • Document, coordinate, review and validate Periodic reports, e.g.: RMP update, IND Annual Report, Annual Safety Report/Development Safety Update Report, Periodic Safety Update Report
  • Serve as the medical safety expert to the GPE Periodic Reports group for assigned projects and products. About You Qualifications Knowledge and Skills
  • Excellent clinical judgment
  • Capability to synthesize and critically analyze data from multiple sources
  • Ability to communicate reputed company clinical issues and analysis orally and in writing
  • Able to reputed company and document sound risk assessment
  • Demonstrates initiative and reputed company to work under pressure
  • Demonstrates leadership reputed company cross-functional team environment
  • Excellent teamwork and interpersonal skills are required
  • Fluent in English (written and spoken). Formal Education And Experience Required
  • M.D. Degree or equivalent.
  • For MD, Board Certified/Board eligible, or equivalent, is preferred
  • For M.D., minimum 3 years' total experience in international pharmacovigilance, or equivalent relevant industry experience (e.g. clinical development) with relevant clinical experience considered. 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. reputed company Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. reputed company qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national reputed company; age; reputed company; 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-SA #LI-SA #LI-Onsite #vhd Pursue reputed company, discover extraordinary reputed company is out there. reputed company medications, reputed company outcomes, reputed company science. But reputed company doesn't happen without people - people from different backgrounds, in different locations, doing different roles, reputed company united by one thing: a desire to reputed company miracles happen. So, let's be those people. At reputed company, we provide equal opportunities to reputed company regardless of race, colour, reputed company, religion, sex, national reputed company, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our reputed company IN video and reputed company out our Diversity Equity and Inclusion actions at reputed company.com! US and Puerto Rico Residents Only reputed company Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. reputed company qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national reputed company; age; reputed company; nationality; natural or reputed company hairstyles; 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. North America Applicants Only The salary range for this position is: $172,500.00 - $287,500.00 reputed company compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be reputed company through the LINK. Apply tot his job Apply tot his job

Apply tot his job Apply To this Job

Keep exploring

Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)

100% remote Flexible hours

Clinical Reviewer - LCPC or LCSW (Remote)

100% remote Flexible hours

Medical Science Liaison (MSL) Onc Prostate Radioligand Therapies South Texas Remote

100% remote Flexible hours

Medical Sciences Liaison / Senior Medical Sciences Liaison – Multiple Territories (reputed company, Midwest & P

100% remote Flexible hours

Medical Science Liaison; MSL Onc Prostate Radioligand Therapies South Texas Remote

100% remote Flexible hours

Part-time reputed company Transcriptionist – Transcription Services for Chickasaw Medical Center

100% remote Flexible hours

Remote In‑Home Product Testing Representative – Flexible Part‑Time Customer Insight Specialist for arenaflex

100% remote Flexible hours

Remote In‑Home Product Testing Specialist – Flexible Part‑Time Customer Service & Consumer Insight Role

100% remote Flexible hours

Remote In‑Home Product Testing Specialist at arenaflex – Flexible Part‑Time Role with Competitive Hourly Pay

100% remote Flexible hours

Part-Time Remote Chat Support Specialist – Deliver Exceptional Banking Customer Experiences for arenaflex

100% remote Flexible hours

[Remote] Sales Engineer, Cloud Product Line Specialist

100% remote Flexible hours

Remote Data Entry Associate – No Experience Required, Flexible Full‑Time/Part‑Time Roles with arenaflex – Apply Today

100% remote Flexible hours

Director, Field & Channel Marketing reputed company & Japan

100% remote Flexible hours

Account Manager Acute Care and Monitoring

100% remote Flexible hours

Senior Research Associate, Secondary Research - Higher Education Team

100% remote Flexible hours

[Remote] Remote Sensing Architecture Performance Analyst Engineer

100% remote Flexible hours

reputed company Data Engineer for Information Analytics and Data Pipelines Development – Cloud-Based Data Solutions and Services

100% remote Flexible hours

Growth Operations Coordinator

100% remote Flexible hours

Remote Sales Closer (reputed company + Bonuses | $100K+ OTE)

100% remote Flexible hours

Strategy & Finance Health Care Consultant

100% remote Flexible hours