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: San Diego, CA
- Type: Temp-to-Hire
- Focus: Scientific rigor, collaboration, and innovation
Salary & Benefits
- Salary: $117,746 – $154,351 annually
- Benefits: Medical, dental, equity options, 401(k), professional development
Perks include international conference sponsorships, flexible clinical hours, and access to proprietary scientific libraries.
Equal Opportunity
Our client proudly supports diversity in life sciences and is an equal opportunity employer.