⏳ Last Date to Apply: As soon as possible
Parexel Clinical Trial Leader – FSP Recruitment 2026: Apply Online
Clinical Trial Leader – FSP
Job Overview
Parexel is seeking a dedicated and experienced Clinical Trial Leader (CTL) – FSP to join our remote team in the United States. In this role, you will act as a key member of the Clinical Delivery Team nominated to specific trials within our client’s Evidence Network. You will be fully accountable for the set-up, execution, and delivery of assigned clinical trials, contributing significantly to the client’s pipeline through accurate planning and efficient execution.
- Lead clinical trial activities, steering patient and site engagement initiatives across global, multi-country, or regional bases.
- Collaborate closely with Clinical Trial Managers (CTMs) and functional partners on all study-related issues and risk mitigation.
- Oversee trial preparation, operational feasibility, country allocation, and the development of core trial documents.
- Maintain rigorous oversight during trial conduct, ensuring adherence to GCP, regulatory requirements, and SOP compliance.
- Coordinate trial closeout activities, clinical data cleaning, and timely archiving in the TMF.
Key Job Details
| Company Name | Parexel |
| Job Role | Clinical Trial Leader – FSP |
| Experience | Experienced |
| Salary Range | Competitive |
| Job Type | Full-Time |
| Work Mode | Remote |
| Openings | 1 |
| Job Location | United States – Remote |
Key Responsibilities
- Accountable for accurate planning, operational feasibility, and timely execution of clinical trial timelines.
- Oversee trial preparation, country allocation, and development of core patient-facing and trial-level documents.
- Maintain continuous oversight during clinical trial conduct, ensuring strict adherence to GCP, SOPs, and regulatory compliance.
- Manage vendor services outsourcing, central lab coordination, budget oversight, and safety reporting mechanisms.
- Coordinate timely data cleaning, clinical trial report generation, and complete archiving of global documents in the TMF.
Requirements & Qualifications
- University degree in Biomedical Life Sciences (Bachelor’s or advanced degree).
- Demonstrated clinical trial project management experience in an international or multi-cultural context.
- Understanding of major regulatory frameworks including US FDA, EMA, and PMDA guidelines.
- Strong competencies in agility, accountability, fast decision-making, and outcome-based thinking.
- Excellent communication and leadership skills with a proven ability to empower and guide cross-functional teams.
Required Skills
- Clinical Project Management
- Therapeutic Area Expertise (Oncology / Inflammation)
- Regulatory Compliance (FDA, EMA, PMDA)
- Risk Mitigation & Strategic Mindset
- Cross-Cultural Communication & Leadership
About Parexel
Parexel is a leading global clinical research organization (CRO) providing comprehensive drug development, clinical trial management, and consulting services to the pharmaceutical, biotechnology, and medical device industries. Committed to a patient-first culture, Parexel combines innovative technology and scientific expertise to help accelerate the delivery of life-changing treatments to patients worldwide.
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