Manager, Safety Scientist

BeOne Medicines; United States; On-site; USD 128,000 - 168,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

401(k)

Job summary

BeOne Medicines is seeking a Manager, Safety Scientist to lead safety data evaluation, signal detection and regulatory reporting for assigned compounds. You will work with Product Safety Leads to ensure compliance with global regulations and internal processes.

You will interact with cross-functional teams and safety governance bodies, presenting safety data and contributing to strategic safety decisions on multiple programs.

Qualifications

• PharmD, RN or PhD/MS in a medical field or biological science and 2+ years in pharmacovigilance.
• Pharmaceutical product development experience.
• Knowledge of global regulatory requirements for pharmacovigilance.

Responsibilities

• Support signal detection and evaluation of safety data.
• Prepare safety assessments and risk analyses.
• Interface with PSLs and cross-functional teams to ensure thorough evaluation.
• Assist with regulatory submissions and safety sections of documents.
• Contribute to safety governance meetings and safety communications.

Skills

Signal detection

Safety data evaluation

Regulatory inquiries

Cross-functional collaboration

Education

PharmD, RN or PhD/MS in a medical field or biological science

Tools

Argus safety database

MedDRA

Excel

PowerPoint

Word

Veeva

Spotfire

PowerBI

Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description

The Manager, Safety Scientist supports assigned compounds in conjunction with Product Safety Leads (PSLs) to conduct signal detection, evaluation of safety data, assessment of safety risks, responses to regulatory inquiries, and regulatory-required periodic reporting. In this role, you will apply effective prioritization, critical thinking, and judgment-based decision making to execute these key deliverables in compliance with global regulations and internal processes. Effective communication and influence with internal and external stakeholders is an important capability for this role. This role represents GPS Safety Science internally and externally at a global level and functions as an authoritative and professional member of relevant teams.

Essential Functions Of The Job

Signal and Safety Data Evaluation

• Support the identification, analysis, and evaluation of safety data for signal detection from all applicable sources
• Perform signal detection and signal assessment along with required documentation following BeiGene process
• Support and propose data acquisition strategy, methodology, and approach for safety evaluations
• Support analysis of safety data and author safety assessment
• Collaborate with PSLs, scientists, pharmacoepidemiologists, and other cross functional personnel as appropriate to ensure thorough evaluation and aggregate analysis of safety data, demonstrating the ability to understand and communicate scientific issues and strategy
• Execute signal assessment analysis per strategy and assist with the preparation of presentations for Safety Management Team and Company Safety Committee
• Support the preparation and presentation of safety data at safety governance meetings (Safety Management Team and Company Safety Committee) and for Safety Monitoring Committee (SMC), Data Monitoring Committee (DMC)/Data and Safety Monitoring Board (DSMB)
• Apply judgment-based decision-making principles to contribute to key scientific/clinical discussions
• Apply effective communication skills to lead and facilitate safety team meetings
• Communicate relevant safety information to core team, business partners, and key stakeholders in a timely manner
• Support the development, update, and review of safety communication documents (e.g., Dear Investigator Letter, Informed Consent Form, Investigator's Brochure, Healthcare Professional communications [DHCP letter or DHPC], Labelling documents, Risk Management Plan, etc.) in collaboration with Safety Science team members and relevant cross-functional team members

Clinical Trial Support

• Support the review of safety data and monitor the safety of patients on allocated clinical trials
• Support the writing and review safety sections and provide safety expertise for development of Protocols, IBs, ICFs, Safety Analysis Plans (SAPs), Tables Figures and Listings (TFLs), Medical Monitoring Plans, CSRs (incl. China ADR Summary) and other relevant project/study documents and answer ad-hoc safety queries from ethics committees
• Contribute to safety sections and review aggregate reports, e.g., PBRERs, DSURs, PADERs
• Support the authoring and review of safety sections of regulatory submissions, e.g., IND/CTA (General Investigational Plans, China Risk Control Plans), NDA/MAA (SCS/ISS, RMPs, initial Package Inserts) collaborating with PSLs and other Clinical Study Team (CST) members
• Support the authoring of Storyboards and Briefing Books for HA interactions
• Support ad-hoc review of the Safety Management Plans
• Support investigator training

Risk Assessment, Regulatory Inquiries, and Periodic Reporting

• Assist with analysis of safety data and author relevant safety sections of global regulatory inquiries and periodic reports including Development Safety Update Reports (DSURs), Periodic Adverse Drug Experience Report (PADER)/Periodic Adverse Experience Report (PAER), Periodic Safety Update Reports (PSURs), Periodic Benefit Risk Evaluation Reports (PBRERs), and Risk Management Plans (RMPs)
• Provide high quality support for additional evaluation requests from health authorities (e.g., PRAC PSUSA) for assigned compounds
• Support strategy development, analysis, and response to safety questions from health authorities, IRBs/ECs.
• Assist with integrated Benefit/Risk assessments

Promote and Advance the Field of Pharmacovigilance

• Any other tasks assigned by manager to assist in departmental activities

Supervisory Responsibilities

• The position has no direct reports. The Manager, Safety Scientist is part of a team that performs high quality and timely scientific and operational safety analysis. This position works closely with the Safety Scientist group as part of a matrix team to conduct safety assessment and safety risk management activities per BeiGene process and applicable regulations.

Computer Skills

• Knowledge working with a safety database (i.e., Argus) for retrieval of safety information
• Intermediate knowledge of MedDRA and signal management system
• Advanced application capability with Excel, PowerPoint, Word, and electronic document management system (i.e., Veeva)
• Familiarity with data mining tools and analyses tools such as Spotfire and PowerBI

Qualifications

• PharmD, RN or PhD/ MS in a medical field or biological science and 2+ years as a Safety (Pharmacovigilance) Scientist.
• Pharmaceutical product development experience
• Experienced in global regulatory requirements for pharmacovigilance

Travel

• Less than 10%

BeOne Global Competencies

• Fosters Teamwork
• Provides and Solicits Honest and Actionable Feedback
• Self-Awareness
• Acts Inclusively
• Demonstrates Initiative
• Entrepreneurial Mindset
• Continuous Learning
• Embraces Change
• Results-Oriented
• Analytical Thinking/Data Analysis
• Financial Excellence
• Communicates with Clarity

Global Competencies

• Fosters Teamwork
• Provides and Solicits Honest and Actionable Feedback
• Self-Awareness
• Acts Inclusively
• Demonstrates Initiative
• Entrepreneurial Mindset
• Continuous Learning
• Embraces Change
• Results-Oriented
• Analytical Thinking/Data Analysis
• Financial Excellence
• Communicates with Clarity

Salary Range: $127,800.00 - $167,800.00 annually

BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact [e-mail].