This is what you will do:
The Associate Director, Safety Scientist
plays a leadership role within Global Patient Safety (GPS) to actively evaluate and manage risk in collaboration with the GPS Medical Director(s) and cross-functional team members within the global regulatory framework.
You will be responsible for:
Managing safety scientist activities across multiple product portfolios and/or indications
Organizing, training and/or supporting junior safety scientists and fellows
Supporting activities related to new drug applications and other regulatory filings
Representing global patient safety at regulatory inspections e.g., MHRA, FDA, EMA, etc.
Leading gap analysis to ensure alignment with changes in global regulations
Strategizing and drafting of responses to regulatory inquiries on product safety issues inclusive of defining MedDRA search strategy
Presenting GPS in global program teams and associated cross functional teams and/or projects as needed
Proactively providing guidance and educational training to GPS therapeutic teams
Participating in ongoing safety data review and analysis for products in designated therapeutic areas
Performing Signal Surveillance activities for respective programs in collaboration with GPS Medical Directors
Project managing and authoring of safety documents including PSUR, PBER, PADER, RMP, REMS, CSRs, and ad hoc requests in collaboration with GPS Medical Directors
Authoring safety sections, in collaboration with team members, on regulatory responses, IBs/CCDS, protocols, ICFs, Data Monitoring Committee reports and requests, and other documents, and provide the necessary quality control to ensure alignment with core safety position
Manage portfolio of products/projects related to risk management; assists GPS Medical Directors in the development of risk management strategy and activities for assigned products
Contribute to on-going process enhancement for safety analytics and reporting, such as developing standard procedures and templates
Assisting GDS Medical Directors to oversee risk minimization activities including tracking of activities as needed
May be directed by the line function to support initiatives outside of their projects
You will need to have:
Bachelors degree in a biologic/medical/clinical/nursing field
At least 5 years experience in drug safety and risk management within the pharmaceutical, biotech or CRO industry
Knowledge and understanding of US and EU safety regulations pre- and post-marketing
Experience with Risk Management and Minimization programs
Experience preparing post marketing safety regulatory documents including PSURs, PBRERs and Risk Management Plans
Experience with clinical development including risk/benefit analysis and safety assessment
Strong clinical, analytical, problem solving and scientific writing and communication skills
Ability to interact effectively with people of multiple disciplines and cultures both within and outside the company on a global basis
Expertise with Microsoft Word, PowerPoint, SharePoint and Excel
The duties of this role are generally conducted in an office environment. As is typical of an office-based role, employees must be able, with or without an accommodation to:
Use a computer;
Engage in communications via phone, video, and electronic messaging;
Engage in problem solving and non-linear thought, analysis, and dialogue;
Collaborate with others;
Maintain general availability during standard business hours.
We would prefer for you to have:
Advanced degree in a biologic/medical/clinical/nursing field preferred: Pharmacist/PharmD, Nurse Practitioner or PhD
Expertise with clinical and safety databases
Experience in MedDRA coding and search strategies
Excellent, independent judgment based on knowledge and expertise
Strong personal time-management and project-management skills
Mastery of Microsoft Word, PowerPoint and Excel
Date Posted: 11-sept-2024
Closing Date:
Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact.
Alexion participates in E-Verify.
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