Associate Medical Director, Global Drug Safety (Alexion)

Alexion Pharmaceuticals, Inc.; Warszawa; On-site; PLN 338,000 - 508,000; Full time

Job summary

A global biopharmaceutical company is seeking an Associate Medical Director in Warsaw. You will be responsible for executing safety and risk management activities for clinical projects. Ideal candidates have an MD degree and experience in drug safety. Strong analytical and communication skills are essential. This role offers the opportunity to contribute significantly to patient safety and regulatory compliance.

Qualifications

• A minimum of 1 year experience in drug safety and risk management within the pharmaceutical industry or 3 years in a clinical care setting.
• Strong verbal and written communication skills.
• Sound problem-solving skills.

Responsibilities

• Identify and present safety issues at meetings.
• Assist in preparation of safety data for governance meetings.
• Conduct medical reviews of safety reports.

Skills

Excellent judgment

Verbal communication

Written communication

Problem-solving

Knowledge of drug safety regulations

Education

MD or equivalent degree

Tools

Microsoft Word

Microsoft PowerPoint

Microsoft Excel

Job description

This is what you will do:

The Associate Medical Director, Global Drug Safety is accountable for executing the safety and risk management activities for one or more assigned clinical development projects or marketed products to enable the safe and effective use of Alexion’s products by patients and healthcare providers. The Associate Medical Director will be responsible for safety activities for investigational products and/or marketed, including identification and evaluation of safety signals and risk management to drive decision‑making on risk/benefit evaluation. The Associate Medical Director, Global Drug Safety is an individual contributor role and will be supervised by Medical/Senior/Executive Director, Global Drug Safety.

You will be responsible for:

• Through data review and research, identifies and presents at Safety Management Team meetings, safety issues for further review and analysis
• Assists in preparation of safety data for DSMBs and other safety governance meetings
• Represents GDS on other project/product team(s) or subteam(s) as a key cross‑functional member and subject‑matter expert
• Detects, validates and manages pre‑and/or post‑approval safety signals through to resolution
• Conducts medical review of Individual Case Safety Report (ICSR) and analysis of similar events (AOSE) as necessary, including the assessment of quality within the ICSR process; identifies process improvement opportunities and drives changes in process
• Evaluates aggregate safety data and provides contributions to core regulatory documents i.e. Periodic Safety Update Reports, Drug Safety Update Reports, Risk Management Plans,
• and other routine and non‑routine safety and risk/it evaluations for internal or regulatory purposes as required
• Identifies, initiates and manages to completion, necessary safety updates to the IB, CCSI and/or local product information, Medication Guide, Patient Leaflet, and other labeling documentation as necessary
• Assist in regulatory responses to safety inquiries from regulatory agencies
• May be directed by the line function to support initiatives outside of their projects

You will need to have:

• MD or equivalent degree required
• A minimum of 1 year experience in drug safety and risk management within the pharmaceutical, biotech or CRO industry or 3 years within a clinical care setting
• Excellent, independent judgment based on knowledge and expertise
• Strong verbal and written communication including making recommended courses of action to management and/or senior leaders that impact the discipline, department or line, and influences their decisions.
• Sound problem solving skills including the ability to make decisions by developing innovative options and/or multiple solutions to highly complex problems
• Expertise with Microsoft Word, PowerPoint and Excel

We would prefer for you to have:

• Rare, ultra‑rare or orphan disease area experience
• Strong personal time‑management and project‑management skills
• Knowledge and understanding of US and EU safety regulations, CIOMS, ICH and GCP guidelines
• Clinical development /research experience is preferred
• Broad and deep knowledge of the principles, concepts, and theories of drug‑induced disease for therapeutic/product area(s)

Date Posted: 12‑lis‑2025

Closing Date: 28‑lis‑2025

Alexion is proud to be an Equal Employment Opportunity and affirmative action employer. We are committed to fostering a culture of belonging where every individual 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, 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 request accommodations, please contact [e-mail]. Alexion participates in E‑Verify.