Drug Safety Scientist

Fresenius Kabi; Lake Zurich (IL); Presencial; USD 110.000 - 115.000; Tempo integral

Benefícios oferecidos por esta vaga

Bonus plan 6% target

401(k) with company contributions

Health benefits (medical, dental, VIs)

Resumo da vaga

Fresenius Kabi in the United States seeks a Drug Safety Scientist to receive, assess, and report adverse drug events, coordinating with global teams and supporting case intake. The role emphasizes regulatory compliance and high-quality data interpretation.

Applicants should hold a clinical degree with 3+ years in drug safety, and possess strong communication and collaboration skills. Fresenius offers a comprehensive benefits package and a target bonus, reflecting a strong team culture.

Qualificações

• Minimum 3 years of drug safety and adverse drug safety reporting experience.
• Holds a current medical/clinical professional degree in good standing (e.g., Pharm D, RPH, RN).
• Experience with FDA regulations, safety guidelines, and SOPs relevant to ADEs.
• Experience with PADER preparation is preferred.
• Ability to gather data from multiple sources to build accurate narratives.

Responsabilidades

• Receives, assesses, follows up, and processes adverse drug events per regulations and SOPs.
• Oversees PADER preparation with Global Vigilance and coordinates FDA submissions.
• Collaborates with internal/external teams and stakeholders.
• Performs complex ADE case intake and quality checks for regulatory submission.
• Performs additional tasks as required; adheres to Health, Safety, Environment, and Quality Systems.

Conhecimentos

Safety reporting

Regulatory knowledge

Cross-functional collab

Communication skills

Attention to detail

Problem solving

Data interpretation

Formação

Pharm D

RPH

RN

Ferramentas

Aris Global

Microsoft Office

Descrição da vaga

Job Summary

The Drug Safety Scientist receives, assesses, obtains follow-up, processes, and reports adverse drug events regarding company drug products. Participates in global data exchange with Fresenius Kabi entities and other Fresenius Kabi USA partners. Collaborate with internal and external FK teams to facilitate case intake.

Salary Range: $110,000-$115,000 based on experience

• Position is eligible to participate in a bonus plan with a target of 6% of the base salary (include only if applicable to the grade level)
• Final pay determinations will depend on various factors, including, but not limited to, experience level, education, knowledge, skills, and abilities.
• Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most. Benefits offered include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage.

Applicants must be authorized to work for ANY employer in the United States. Fresenius Kabi is unable to sponsor or take over sponsorship of an employment visa either now or in the future.

Responsibilities

Receives, assesses, obtains follow-up, and performs case intake for adverse drug events in accordance with global and local regulations and SOPs.

Oversees preparation of adverse event Periodic Adverse Drug Experience Reports (PADER) with Global Vigilance and coordinates timely FDA submissions with Regulatory Departments.

Collaborates cross-functionally with internal and external teams and stakeholders.

Performs complex ADE case intake and performs quality check for submission to regulatory authority

Performs additional tasks and responsibilities as required.

All employees are responsible for ensuring the compliance to company documents, programs and activities related to the Health, Safety, Environment, Energy, and Quality Management Systems, as per your roles and responsibilities.

Requirements

• Minimum 3 years of drug safety and adverse drug safety reporting experience preferred.
• Holds a current medical/clinical professional degree in good standing required i.e. Pharm D, RPH, RN degree.
• Clinical/hospital experience preferred.
• Demonstrated ability to interpret and apply FDA regulations, global and local safety guidelines, and internal SOPs to the assessment and processing of adverse drug events, including identification of potential product quality issues.
• Experience with preparation of adverse event Periodic Adverse Drug Experience Reports (PADER) is preferred.
• Proficiency in gathering and evaluating data from multiple medical and regulatory sources to develop accurate and medically sound case narratives.
• Experience with Aris Global systems is a plus.
• Dynamic highly motivated professional with the ability to work cross-functionally and collaboratively.
• Ability to analyze safety and quality-related data to identify potential health risks (signal detection).
• Working knowledge of PC-based systems, adverse event safety databases, and Microsoft Office applications.
• Strong critical thinking and problem-solving abilities; able to work independently while effectively managing multiple priorities.
• Ability to collaborate cross-functionally and participate in peer review processes.
• Maintains a high level of attention to detail while performing complex case assessments.
• Demonstrates professionalism and interpersonal effectiveness consistent with company values.
• Excellent written and verbal communication skills required.

• The Company’s primary business language is English. The successful candidate must be able to effectively speak, read, write, and understand English to perform the essential functions of the position, including independently understanding policies, procedures, training materials, and workplace communications written in English due to our heavily regulated work environment.

Additional Information

We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability,401K with company contribution, andwellness program.

Please note that joining our team does not create a guaranteed or permanent employment arrangement. All employment is at‑will, meaning both the employee and Fresenius Kabi have the right to end the employment relationship at any time, in accordance with applicable federal and state laws.

Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.