Company Overview
Our client is a global leader in life sciences innovation, dedicated to advancing healthcare outcomes through groundbreaking research, clinical integrity, and patient-focused operations.
Key Responsibilities
- Lead scientific, regulatory, or research operations based on role scope.
- Design and support clinical trial protocols and reporting documentation.
- Collaborate with cross-functional teams including medical, legal, and compliance.
- Present research findings or regulatory updates to external stakeholders.
- Ensure all activities align with ethical and regulatory standards.
Qualifications
- Advanced degree (PhD, PharmD, MD, or equivalent) preferred depending on role.
- 4–10 years of experience in life sciences, clinical research, or regulatory affairs.
- Strong knowledge of FDA, EMA, and GCP guidelines.
- Excellent analytical writing and communication skills.
- Ability to manage multiple projects in a matrixed environment.
Work Environment
- Location: Chicago, IL
- Type: Temp-to-Hire
- Focus: Scientific rigor, collaboration, and innovation
Salary & Benefits
- Salary: $107,632 – $113,178 annually
- Benefits: Medical, dental, equity options, 401(k), professional development