This full-time role focuses on site management, monitoring, and ensuring GCP compliance—ideal for professionals with 1-2 years of experience seeking impactful clinical research careers in biotech and pharma. Salary band: $70,000 – $110,000 (based on experience). Job ID: 3697, posted February 7, 2026.
About the Company
Novotech is a globally recognized full-service contract research organization (CRO) specializing in clinical development services across all phases and therapeutic areas, with a strong focus on biotech. Founded in 1997, Novotech has expanded to 30+ offices across Asia-Pacific, North America, and Europe, employing over 3,000 professionals.
The company excels in oncology, immunology, infectious diseases, rare diseases, and more, delivering high-quality trials while fostering an inclusive, award-winning workplace culture that prioritizes diversity, equity, innovation, and employee well-being.
Job Details
- Company Name: Novotech
- Experience: Approximately 1-2 years as CRA or equivalent in clinical research (CRA II fast track program available)
- Qualification: Relevant experience in clinical research; fully competent in regulatory start-up or monitoring functions
- Location: South San Francisco, CA, United States (400 Oyster Point Boulevard, Suite 401, South San Francisco, CA 94080)
- Work Type: Full-Time (Office/Hybrid elements likely; site visits required)
Job Description
The Clinical Research Associate (CRA) serves as the primary liaison between investigational sites, Novotech, and sponsors. This role ensures participant rights and well-being are protected, trial data are accurate and verifiable, and studies comply with ICH GCP, local/global regulations, and SOPs.
Emphasis is on building strong site relationships for efficient trial execution.
Clinical Research Associate
- Department: Clinical Operations / Site Management
- Market: Global Biotech and Pharma (multi-regional trials)
- Role: Clinical Research Associate (CRA)
- Experience: 1-2 years CRA or equivalent; high autonomy expected
- Education/Qualification: Clinical research experience; regulatory start-up competency
Skills/Qualifications
- Proven ability to build and maintain relationships with Principal Investigators, study coordinators, pharmacists, and site staff
- Strong knowledge of ICH GCP guidelines, regulatory requirements, and SOPs
- Experience in site essential document preparation, ethics/regulatory submissions
- Competence in quality study management and monitoring with moderate oversight
- Excellent communication, organizational, and problem-solving skills
- Ability to work autonomously while collaborating internally and externally
- Passion for clinical research and biotech
Key Responsibilities
- Build and foster relationships with site personnel for smooth trial management
- Support site essential documents, ethics, and regulatory submissions/approvals
- Participate in CRA II fast track training, observational visits, and on-the-job mentoring
- Manage quality monitoring and deliverables at country/site level per project rules
- Provide mentorship to junior staff and support line/project managers as needed
- Ensure timely, productive project delivery focused on sponsor requirements
Benefits/Perks
- Competitive salary: $70,000 – $110,000 based on experience
- Flexible working options and generous leave entitlements
- Paid parental leave for both parents
- Wellness programs and ongoing professional development
- Inclusive environment supporting diversity (LGBTIQ+, disabilities, carers)
- Circle Back Initiative Employer—commitment to respond to every application
How to Apply
Apply directly through Novotech’s careers portal. Visit Novotech Careers – Current Opportunities and search for Job ID 3697 or “Clinical Research Associate” in United States.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Novotech Career page.
Submit your application promptly—Novotech commits to reviewing every submission. For similar clinical research jobs, CRA positions, and opportunities in the US/India, explore .
Why You Should Join
Novotech offers a supportive, growth-oriented environment in the dynamic biotech CRO space. Benefit from specialized training (like CRA fast track), mentorship from experienced leaders, and opportunities to advance in clinical operations.
With a global footprint and focus on innovation, inclusion, and work-life balance, it’s an excellent choice for building a rewarding career in pharmaceutical careers and clinical research while contributing to life-changing therapies.
