At a Glance
- Tasks: Lead clinical trials, ensuring timelines and deliverables are met while collaborating with diverse teams.
- Company: Dynamic healthcare company focused on innovative virology research.
- Benefits: Flexible work schedule, competitive salary, and opportunities for professional growth.
- Other info: Join a supportive team committed to diversity and inclusion.
- Why this job: Make a real difference in healthcare by managing impactful clinical studies.
- Qualifications: Bachelor's degree in relevant field and 5+ years in clinical project management.
The predicted salary is between 60000 - 75000 £ per year.
Responsibilities
- Plan, direct, create and communicate clinical study timelines to ensure deliverables are produced on schedule.
- Gather input from cross‐functional teams to develop comprehensive plans for clinical studies.
- Ensure consistency of clinical study processes across trials, adhering to SOPs, GCP and country regulations.
- Oversee and resolve operational aspects of clinical trials, identifying and addressing issues that arise.
- Select sites and vendors, prepare clinical trial budgets, and ensure studies are conducted within protocol and allocated resources.
- Monitor progress, identify deviations and work with team members to apply corrective actions.
- Implement and prepare the clinical development strategy in alignment with clinical teams.
- Develop and execute trial recruitment strategies to achieve participant enrollment targets.
Qualifications
- Bachelor's degree in Clinical Research, Life Sciences, Healthcare Management or a related field.
- Minimum of 5 years of experience in clinical project management or a related role.
- Proven track record of successfully managing clinical trials and ensuring adherence to SOP, GCP and country regulations.
- Certification in Clinical Research (e.g., CCRP, CCRA) – preferred.
- Project Management Professional (PMP) certification – a plus.
Required Skills
- Strong organizational and planning skills for creating and managing study timelines.
- Excellent communication skills for gathering input and conveying plans.
- Capability to oversee and resolve operational issues during trials.
- Deep knowledge of SOP, GCP and country regulations for consistency across studies.
- Experience in site and vendor selection, budget preparation and monitoring.
- Ability to implement and prepare clinical development strategies.
- Strong problem‐solving skills to address challenges that arise during clinical trials.
We are committed to the Americans with Disabilities Act and the European Union Equality Directive, providing reasonable accommodations to assist employees or applicants to perform the essential functions of this position. All applications are received under the same standards and without discrimination.
Single Sponsor Clinical Project Manager II (Virology) - 3 days a week in Uxbridge. in London employer: Syneos Health, Inc.
As a leading employer in the clinical research field, we offer a dynamic work environment in Uxbridge that fosters collaboration and innovation. Our commitment to employee growth is reflected in our comprehensive training programmes and support for professional certifications, ensuring that you can advance your career while contributing to impactful virology studies. With a strong focus on work-life balance, our flexible three-day work week allows you to thrive both personally and professionally.
