Global Safety Officer in Bridgewater, NJ

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 • Lead cross functional Safety Management Teams (SMTs) and GPE internal Safety Analysis Teams (SATs) • Communicate with and represent PV position within 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. • Lead aggregate safety data review activities and coordinate safety surveillance activities Impact: • Signal detection and analysis • Development of safety action plans and implementation, as appropriate • Enable effective development of product safety • Enable appropriate risk management • Enable up-to-date risk communication (e.g. labeling)

Risk Assessment/Risk Management/ Benefit-Risk Assessment: • Provide proactive risk assessment • Co-lead benefit-risk assessment with other relevant functions • Develop risk management strategies and plans and monitor effectiveness • Collaborate with Center of Excellence for Risk Management and Safety Epidemiology Impact: • Optimization of the product benefit risk profile • Development of REMS, Risk Management and Development Risk Management plans • Identification and implementation of risk mitigation or other corrective actions as necessary • Regulatory compliance • Monitoring of risk mitigation tool effectiveness and adjustment of strategy, as needed

Submission Activities: • Represent safety position in cross functional submission teams • Ensure generation, consistency, and quality of safety sections in submisssion documents • Write responses or contributions to health authorities’ questions • Support preparation and conduct of Advisory Committee meetings Impact: • Review, data analysis, preparation and/or contribution, and/or update of safety sections of relevant documents: • For products under clinical development: Clinical Development Plan, study protocol, Statistical Analysis Plan, data monitoring plan, investigator brochure, Informed Consent Form, study report, Integrated Summary of Safety, Summary of Clinical Safety, risk management plan, label, periodic reports • For marketed products: Response to health authority question/request for information, Core Safety Information updates, periodic reports

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. Impact: • Regulatory Compliance.

Non-MD GSO can only be assigned to the following product areas: generics, consumer healthcare, vaccines and “mature products”, where mature products are defined as those no longer under patent or other data exclusivity protection AND where there is no on-going significant investment in development or marketing.

Required:

• Ability to communicate complex clinical issues and analysis orally and in writing
• Excellent clinical judgment
• Capability to synthesize and critically analyze data from multiple sources
• Able to develop and document sound risk assessment
• Demonstrates leadership within cross-functional team environment

Rangam Consultants is a minority, women-owned, disability workforce solutions global organization. Specialized in attracting and retaining talents globally for a rewarding career in IT, Engineering, Scientific, Clinical, Healthcare, Administrative, Finance, Business Management, and many more, while integrating veterans and individuals with disabilities into the workforce. Indeed, we connect career aspirants to relevant job opportunities, be it jobs in USA, UK, India, or Ireland. Also remote jobs, work-from-home jobs, or contract jobs in different verticals and industries.
Rangam strives to put job seekers first, giving them free access to search for jobs, post resumes, and research companies.Every day, we connect millions of people to new opportunities.