At a Glance
- Tasks: Lead clinical trials, ensuring timelines and deliverables are met while collaborating with diverse teams.
- Company: Dynamic healthcare organisation focused on innovative virology research.
- Benefits: Flexible work schedule, competitive salary, and opportunities for professional growth.
- Other info: Join a supportive team committed to inclusivity and career development.
- Why this job: Make a real difference in healthcare by managing impactful clinical studies.
- Qualifications: Bachelor’s degree in relevant field and 5 years of clinical project management experience.
The predicted salary is between 50000 - 60000 £ 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.
Certifications:
- 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. 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 opportunities for advancement, ensuring that you can thrive in your career while contributing to impactful virology studies. With a strong focus on work-life balance, including a flexible three-day work week, we prioritise the well-being of our team members, making us an exceptional place to build a meaningful career.
StudySmarter Expert Advice🤫
We think this is how you could land Single Sponsor Clinical Project Manager II (Virology) - 3 days a week in Uxbridge.
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who have experience with virology. A friendly chat can lead to insider info about job openings or even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of SOPs and GCP regulations. We want you to showcase your expertise in managing clinical trials, so practice articulating your past experiences and how they align with the role.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that resonate with your values and career goals. Use our website to find roles that excite you, and tailor your approach to each one!
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you top of mind and show your enthusiasm for the position. Plus, it’s a great chance to reiterate why you’re the perfect fit for the team.
We think you need these skills to ace Single Sponsor Clinical Project Manager II (Virology) - 3 days a week in Uxbridge.
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the role of Clinical Project Manager II. Highlight your experience in managing clinical trials, especially in virology, and showcase your knowledge of SOPs and GCP. We want to see how your skills align with what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical project management and how your background makes you a perfect fit for our team. Don’t forget to mention your problem-solving skills and experience with cross-functional teams.
Showcase Relevant Experience:When filling out your application, be sure to highlight your relevant experience in clinical project management. Include specific examples of how you've successfully managed timelines, budgets, and operational issues in past roles. We love seeing concrete achievements!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about StudySmarter and what we stand for!
How to prepare for a job interview at Syneos Health, Inc.
✨Know Your Clinical Trials Inside Out
Make sure you brush up on your knowledge of clinical trial processes, especially in virology. Be ready to discuss specific trials you've managed, the challenges you faced, and how you ensured compliance with SOPs and GCP. This will show your expertise and confidence.
✨Showcase Your Organisational Skills
Prepare examples that highlight your strong organisational and planning skills. Discuss how you've created and managed study timelines in previous roles, and be ready to explain how you monitor progress and implement corrective actions when needed.
✨Communicate Effectively
Since excellent communication is key for this role, practice articulating your thoughts clearly. Think about how you gather input from cross-functional teams and convey plans. You might even want to prepare a few questions to ask the interviewers about their communication processes.
✨Demonstrate Problem-Solving Prowess
Be prepared to discuss specific operational issues you've encountered during trials and how you resolved them. Highlight your problem-solving skills and your ability to adapt strategies to meet participant enrollment targets or address deviations in study protocols.
