<div class="show-more-less-html__markup show-more-less-html__markup--clamp-after-5 relative overflow-hidden"> <p><strong>We're working with a CRO whose seeking a Project Manager with 5+ years of CRO project management experience and a strong understanding of the full clinical trial lifecycle.</strong></p><p><br/></p><p><br/></p><p><strong>Key Responsibilities</strong></p><p>- Lead clinical trials from study start-up through closeout</p><p>- Manage sponsor relationships and cross-functional project teams</p><p>- Oversee timelines, budgets, risks, and study deliverables</p><p>- Coordinate activities across Clinical Operations and must have strong experience in Medical Writing, Data Management, and Quality Assurance</p><p>- Ensure compliance with ICH-GCP, regulatory requirements, and company SOPs</p><p>- Drive project success through effective communication, planning, and problem-solving</p><p><br/></p><p><br/></p><p><strong>Requiremen</strong>ts- Minimum 5 years of experience within a CRO</p><p>- Proven experience managing all aspects of clinical trials</p><p>- Hands-on knowledge of Medical Writing, Data Management, Quality Control, and Clinical Operations- Strong understanding of ICH-GCP and regulatory requirements</p><p>- Excellent project management and stakeholder management skills</p><p><br/></p><p><strong>If interested please apply with your updated CV and I'll be in touch within 48 hours</strong></p> </div>