The Clinical Lead will provide leadership and oversight for site management and clinical monitoring activities across multi-regional studies. The Clinical Lead role is ideal for an experienced clinical research professional with strong CRA leadership and site management experience.
The Clinical Lead role is a direct placement opportunity and allows you to work remote in the United States. Responsibilities of the Clinical Lead:- Lead site management and monitoring activities across multiple study sites and regions.
- Support feasibility assessments, site identification, and site selection activities.
- Assist with ethics and regulatory submission preparation and approval tracking.
- Coordinate investigational product (IP) import/export requirements and shipments.
- Lead internal CRA meetings and provide study updates.
- Attend sponsor meetings and communicate clinical operations progress.
- Mentor and coach CRAs and clinical operations team members.
Requirements of the Clinical Lead:- 5+ years of clinical research experience with advanced monitoring and site management responsibilities.
- Experience leading clinical activities across multiple sites and regions.
- Strong knowledge of ICH-GCP guidelines and clinical trial operations.
- Experience with regulatory and ethics submissions.
- Proven leadership, mentoring, and communication skills.
Compensation for the Clinical Lead:- Salary range: $135,000 - $165,000 + Bonus
- Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.
Keywords:
Clinical Lead, Regional Clinical Lead, Senior CRA, Clinical Research Associate, Clinical Operations, Clinical Monitoring, Site Management, Clinical Trials, ICH-GCP, Regulatory Submissions, Ethics Committee, Sponsor Management, CRO, Biotechnology, Life Sciences, Investigational Product, Study Start-Up, Global Clinical Trials, Oncology, Clinical Research
This job opens for applications on 09/25/2026. Applications for this job will be accepted for at least 30 days from the posting date.
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