Global Product Safety Science Lead

Sobi; Basel; On-site; CHF 190,000 - 250,000; Full time

Job summary

Sobi is seeking a Global Product Safety Science Lead to own product-level safety across the lifecycle. The role combines scientific leadership with hands-on execution, driving safety strategy and leading critical safety deliverables within cross-functional teams.

You will chair safety discussions, oversee signal detection and risk management, and ensure safety considerations are integrated into development decisions in line with GVP and global regulations.

Qualifications

• MD/PhD/PharmD or Master’s in Life Sciences/Public Health.
• Extensive pharmacovigilance and safety science experience in pharma/regulatory.
• Strong knowledge of global PV regulations (GVP, ICH E2E).
• Ability to analyze and interpret medical safety data with scientific rigor.
• Proficiency in Excel, SQL, and data visualization tools (Power BI/Spotfire).
• Experience leading cross-functional global product safety teams and safety strategy.
• Experience collaborating with partner companies for global markets.
• Experience presenting medical safety information at health authority meetings.

Responsibilities

• Lead safety strategy and ownership for assigned products across lifecycle.
• Perform and lead signal detection, evaluation, validation and escalation.
• Drive benefit-risk evaluations and risk-management strategies.
• Oversee key safety deliverables (PSURs, DSURs, RMPs) and regulatory responses.
• Translate safety data insights into actionable guidance for development and regulatory interactions.
• Lead clinical safety science interactions with partners and MDT collaboration.
• Chair product-level safety engagements and represent safety in governance councils.
• Mentor safety team members and develop capabilities within Safety Science.

Skills

Safety science

Pharmacovigilance

Signal detection

Data visualization

SQL

Power BI

Leadership

Cross-functional collaboration

Education

MD/PhD/PharmD

Life sciences degree

Tools

Excel

SQL

Power BI

Veeva Vault

Job description

Sobi is an international biopharmaceutical company, dedicated to providing access to innovative treatments that transform life for people with rare diseases in the areas of haematology, immunology and specialty care. With our head office in Stockholm, Sweden, Sobi also has premises in Basel, Switzerland. You can find more information about Sobi at www.sobi.com .

The Global Product Safety Science Lead (GPSSL) is responsible for performing and leading safety surveillance and benefit–risk activities for one or more assigned products across the product lifecycle.

This role combines scientific leadership and hands‑on execution and represents the primary product‑level safety owner.

The GPSSL drives safety strategy implementation in collaboration with other colleagues within Safety Science, chairs benefit–risk discussions and ensures high‑quality safety deliverables within cross‑functional product teams, including active participation in the Medical Development Team (MDT), ensuring that safety considerations fully integrated into development and lifecycle decisions, in compliance with GVP, GCP and global regulatory requirements.

The GPSSL works collaboratively with other members of the Sobi Global Pharmacovigilance team, and other internal functions across Sobi or externally to ensure proactive safety management, high‑quality regulatory safety deliverables and effective communication of clinical safety throughout the product lifecycle.

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.
• 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.

Qualifications

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
• 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
• 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