Senior Manager, Safety Data Science (FTC Maternity Cover)

Reposted 12 Days Ago
Be an Early Applicant
Bucharest, București, ROU
Hybrid
Senior level
Healthtech • Pharmaceutical
The Role
Lead safety surveillance and signal detection for assigned products across their lifecycle. Analyze clinical, database, and literature data to assess safety, prepare regulatory and leadership summaries, author global aggregate safety reports, advise on benefit-risk and labeling, collaborate with cross-functional teams, and mentor junior safety scientists.
Summary Generated by Built In
Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

The Senior Manager, Safety Data Science partners with cross functional stakeholders in support of the product safety profile and benefit risk throughout product lifecycle through signal detection, signal evaluation, and preparation of written and verbal summaries of signal management activities and risks to patient safety to present to senior management and regulatory authorities globally. 

  • Responsible for standard surveillance activities for a product’s life cycle (one or more assigned compounds and products) through review of safety data from clinical trials, safety databases, and the literature.
  • Collaborates with safety and clinical teams to develop strategies and approaches for signal assessments and regulatory requests by analyzing data from multiple sources.
  • Independently analyzes data for signal assessment and leads preparation of materials of ad hoc regulatory safety requests using data from multiple sources.
  • Utilizes medical judgment to determine the impact of the safety issue on the product’s benefit-risk profile.
  • Communicates findings of surveillance activities and safety assessments to product teams and leadership to inform on necessary risk minimization activities, including label changes.
  • Collaborative preparation and maintenance of safety sections of Clinical Summary of Safety, Clinical Study Reports, Company Core Data Sheets and Risk Management Plan.
  • Independently authors, strategizes and reviews global aggregate safety reports in accordance with regulatory requirements and standard operating procedures
  • Independently prepares summaries of key safety data for PST, SRB, senior management, Advisory and other similar meetings
  • Partners to lead safety-related activities/initiatives internal to PPS.
  • Proficient in pharmacovigilance regulations, guidelines, and company standard operating procedures
  • In depth understanding of compounds within assigned therapeutic areas, including safety profile and where applicable, labeling, literature, clinical and regulatory issues.
  • Mentors and trains new safety scientists.

Qualifications

  • Degree in a Health Sciences (e.g., Pharmacy, Epidemiology, Nursing);
  • Knowledge of the drug development process which includes conducting clinical trials, scientific strategy and operations management for the planning, execution and reporting of clinical development programs, regulatory requirements for submission, product launch and post marketing support. 
  • Demonstrates ability to connect regulatory obligations and safety science to support safety decision making.
  • Understanding of tools, standards and approaches used to efficiently evaluate drug safety is desirable.
  • Serves as a resource to cross-functional colleagues by soliciting input and providing recommendations and conclusions. Demonstrates effectiveness in working in a multidisciplinary, matrix team situation.
  • Demonstrates effectiveness in working in a multidisciplinary, matrix team situation
  • Effective oral and written communication skills with the ability to manage multiple projects simultaneously .
  • Microsoft WORD and EXCEL skills and Basic Project Management skills.
  • Able to work independently with minimal direct supervision.

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Skills Required

  • Degree in a Health Sciences (e.g., Pharmacy, Epidemiology, Nursing)
  • Proficiency in pharmacovigilance regulations, guidelines, and SOPs
  • Knowledge of the drug development process including clinical trials and regulatory requirements
  • Ability to connect regulatory obligations and safety science to support safety decision making
  • Understanding of tools, standards and approaches used to evaluate drug safety
  • Experience analyzing safety data from clinical trials, safety databases, and literature
  • Effective oral and written communication skills and ability to manage multiple projects
  • Microsoft Word and Excel skills and basic project management skills
  • In-depth understanding of compounds within assigned therapeutic areas including safety profile and labeling
  • Ability to mentor and train new safety scientists and work independently

AbbVie Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AbbVie and has not been reviewed or approved by AbbVie.

  • Retirement Support 401(k) contributions include a dollar-for-dollar match up to 6% plus an additional annual company contribution tied to age and service. Company-paid life insurance and other financial protections further strengthen long-term security.
  • Parental & Family Support Paid leave programs include up to 12 weeks at 100% for parental leave and separate paid caregiver leave, with eligibility after six months where noted. Adoption and surrogacy reimbursements and family-building resources add further support.
  • Healthcare Strength Health coverage begins on day one with medical, dental, vision, mental health, and prescription benefits, and preventive care covered at 100%. Options such as HSAs/FSAs and coverage for spouses/domestic partners and children up to age 26 broaden accessibility.

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The Company
HQ: North Chicago, IL
50,000 Employees
Year Founded: 2013

What We Do

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuroscience, eye care, aesthetics and other areas of unmet need.

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