Global Product Safety Science Lead

Sobi; United States; Remote; USD 140,000 - 210,000; Full time

Job summary

Sobi seeks a Product Safety leader to oversee safety signal detection, governance and risk management for assigned products. You will drive safety data analysis, regulatory deliverables, and cross-functional collaboration across Medical, Regulatory and External partners.

The role requires strong pharmacovigilance expertise, global regulatory knowledge, and ability to lead cross-functional teams in a fast-paced, international setting; English proficiency and excellent communication are essential.

Qualifications

• MD, PharmD, PhD or Master’s in Life Sciences/Public Health.
• Solid experience in pharmacovigilance and safety science.
• Strong knowledge of global PV regulations (GVP, ICH E2E).
• Proficiency in analyse, synthesize medical & scientific safety data and contribute to interpretation.
• Strong communication & stakeholder collaboration skills.
• Proficiency in Excel, database querying (e.g., SQL), and basic data visualization (Power BI, Spotfire), AI-related tools.

Responsibilities

• Lead safety signal detection and oversight for assigned products.
• Prepare and review safety deliverables (PSURs, DSURs, RMPs).
• Integrate safety into MDT and product lifecycle decisions.
• Lead product safety governance and decision-making (BRTs, BRC).
• Collaborate with external partners on safety deliverables.
• Support regulatory interactions and audits at product level.

Skills

English proficiency

Analytical skills

Communication skills

Leadership

Risk assessment

Cross-functional collaboration

Education

MD

PharmD

PhD

Master’s in Life Sciences/Public Health

Tools

Excel

SQL

Power BI

Spotfire

AI tools

Job description

Product-level safety ownership

• Perform and lead signal detection, evaluation, validation and escalation activities for assigned product(s).
• Set the strategy for safety signal detection methodology, signal tracking and oversight of safety signals for assigned products.
• Drive, perform and document benefit‑risk evaluations and ensure appropriate risk‑management strategies are implemented.
• Lead and perform assessments for the preparation, review and approval of key safety deliverables (e.g. PSURs, DSURs, RMPs, regulatory responses).
• Translate safety data insights into actionable recommendations for product‑level benefit–risk discussions and regulatory interactions.
• Lead the clinical safety science interactions with partner companies for the assigned products (if applicable) ensuring sharing of safety information per the SDEA and the set up and collaborative functioning of the JSMT.
• Provide safety scientific input to ISS Evaluation Committee as required.
• In case of product quality escalations, work cross functionally to understand impacts on patients, and (if required) lead the preparation of a medical impact Health Hazard Assessment statement.

Cross-functional execution (MDT)

• Act as the Safety Science representative in the Medical Development Team (MDT) and ensure integration of safety into product development and lifecycle decisions.
• Provide clinical safety input into study design, conduct, analysis and interpretation, including study‑level Safety Lead responsibilities where applicable.
• Provide medical and pharmacovigilance expertise e.g. for the clinical safety strategy of the product clinical development program, the development of the Target Product Profile (TPP), the development and maintenance of the RSI, including IB and CDS

Governance and decision-making

• Chair product‑level Benefit Risk Teams (BRTs) and ensure effective operation per SOPs.
• Represent the BRT at Benefit Risk Council (BRC).
• Serve as the primary decision-maker for product-level safety issues, including signal validation and escalation.

Collaboration and delivery

• Lead interactions with external partners and service providers related to assigned product safety deliverables.
• Support regulatory interactions, inspections and audits at product level.

People and capability development

• Mentor colleagues and support capability development within the product safety team.

Continuous improvement & data-driven decision making

• Actively use and continuously develop proficiency in safety systems, data visualization tools, and AI‑enabled analyses (e.g. Veeva Vault(s), analytics dashboards) to support robust and efficient signal detection, safety assessments, and decision‑making for assigned products.
• Identify opportunities for process, data and system improvements within Safety Science.

Level of autonomy: works independently with accountability for assigned products, escalating complex or cross‑product issues as appropriate.

Education/Learning Experience/Work Experience

Required:

• MD, PharmD, PhD or Master’s in Life Sciences/Public Health
• Solid experience in pharmacovigilance and safety science within a pharmaceutical or regulatory environment
• Strong knowledge of global PV regulations (e.g., GVP, ICH E2E), pharmacovigilance processes and practices
• Proficiency to analyse, synthesize medical & scientific safety data and contribute to scientific interpretation
• Strong communication & stakeholder collaboration skills
• Proficiency in Excel, database querying (e.g., SQL), and basic data visualization (e.g., Power BI, Spotfire), AI-related tools
• Experience working with development programs and with products with market approvals
• Experience leading cross functional global product safety management teams, successfully delivering medical safety strategy, with experience across safety signal process, aggregate report writing, safety risk communication and safety risk management

Desired:

• Experience working with partner companies to successfully develop and market products across global markets
• Experience presenting medical safety information at Health Authority meetings
• Demonstrated expertise in the understanding, interpretation, and application of various country/regional pharmacovigilance requirements

Skills/Knowledge/Languages

Required:

• High quality written and spoken English
• Strong analytical skills
• Effective communicator (oral, writing, presentations) at all levels of the business
• Ability to work effectively to fulfil ambitious goals
• Sound and balanced judgment skills; able to assess and handle risks; self-confident, proactive and decisive
• Demonstrated ability to lead safety activities and scientific discussions
• Strong team-leadership capabilities. Demonstrated relationship builder both internally and externally; a strong collaborator within PV function, leadership and the wider organisation

Sobi is an international …