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- Tasks: Lead early-phase oncology trials, ensuring compliance and quality from start to finish.
- Company: Join a dynamic midsized pharma company focused on innovative oncology solutions.
- Benefits: Enjoy flexible work options, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact in cancer research while collaborating with top industry professionals.
- Qualifications: 5+ years in clinical operations, strong GCP knowledge, and oncology experience required.
- Other info: Opportunity to mentor junior staff and shape clinical operations across regions.
The predicted salary is between 48000 - 72000 £ per year.
This role will focus on the Early Phase Oncology program in the UK and mainland Europe. To be considered for this position, candidates must have recent experience with early-phase oncology studies at a CRO, biotech, or pharmaceutical company.
Summary
The Senior Clinical Trial Manager oversees clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH guidelines, Good Clinical Practices (GCP), and regulatory requirements. They collaborate with the Clinical Project Manager (CPM), CRO representatives, and vendors to manage clinical studies effectively. Additionally, they may supervise Clinical Trial Managers to ensure deliverables are met on time, within budget, and to quality standards.
- Participate in the planning, implementing, and managing of clinical trials in compliance with industry regulations and ICH-GCP.
- Oversee CROs and clinical trial sites, ensuring timely delivery, meeting recruitment targets, and producing high-quality data.
- Track site visit metrics, data quality concerns, and protocol deviations; conduct oversight visits for compliance evaluation.
- Assist in initiation visits to confirm site training and foster relationships among sponsors, CROs, and investigators.
- Review CRA monitoring reports to ensure protocol and operational compliance; escalate issues for resolution.
- Collaborate with teams for efficient study start-up, identifying risks and ensuring timelines are met.
- Act as a subject matter expert on assigned protocols and manage CRO/site during start-up activities, including contract negotiations and document collection.
- Provide direction to ensure consistency in Clinical Operations processes across trials and regions.
- Work cross-functionally with departments to meet study requirements and timelines.
- Contribute to developing and reviewing study-related documents and deliver trial-specific training.
- Monitor open action items and data trends, addressing issues with CROs to enhance study execution and efficiency.
- Develop and oversee patient recruitment and retention strategies, acting on any deviations from the plan.
Experience
- Minimum of 5 years of clinical operational experience in biotechnology, pharmaceuticals, and CROs.
- Strong understanding of GCP, ICH, GDP, and relevant CFRs; familiarity with MHRA, EMA, and international regulations is a plus.
- Experience with clinical trial site start-up and initiation.
- Proven ability to build and maintain relationships with clinical trial sites and Principal Investigators.
- Strong communication skills for coordinating activities with internal teams, sites, and vendors.
- Proactive in identifying project challenges and proposing corrective actions with minimal supervision.
- Capable of working independently and delivering high-level presentations.
- Knowledge and experience in oncology.
- Previous experience as a Clinical Research Associate (CRA).
Sr Clinical Trial Manager employer: JR United Kingdom
Contact Detail:
JR United Kingdom Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Sr Clinical Trial Manager
✨Tip Number 1
Network with professionals in the oncology field, especially those who have experience in early-phase studies. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends in clinical trials.
✨Tip Number 2
Familiarise yourself with the specific regulations and guidelines relevant to early-phase oncology trials, such as ICH-GCP and local regulatory requirements. This knowledge will not only boost your confidence but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Prepare to discuss your previous experiences managing clinical trial sites, particularly focusing on how you ensured compliance and met recruitment targets. Use specific examples to illustrate your problem-solving skills and ability to work under pressure.
✨Tip Number 4
Showcase your communication skills by being clear and concise when discussing your past collaborations with CROs and clinical trial sites. Highlight any successful strategies you implemented for patient recruitment and retention, as this is crucial for the role.
We think you need these skills to ace Sr Clinical Trial Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in early-phase oncology studies. Emphasise your roles at CROs, biotech, or pharmaceutical companies, and detail your understanding of GCP, ICH guidelines, and regulatory requirements.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for oncology and your specific achievements in clinical trial management. Mention how your skills align with the responsibilities outlined in the job description, such as overseeing CROs and managing clinical studies.
Highlight Key Achievements: In your application, include specific examples of successful projects you've managed, particularly those involving patient recruitment and retention strategies. Use metrics to demonstrate your impact, such as meeting recruitment targets or improving data quality.
Prepare for Potential Questions: Anticipate questions related to your experience with clinical trial site start-up and your ability to build relationships with investigators. Be ready to discuss how you handle project challenges and ensure compliance with industry regulations.
How to prepare for a job interview at JR United Kingdom
✨Showcase Your Oncology Knowledge
Make sure to highlight your understanding of oncology and any relevant experience you have in early-phase studies. Be prepared to discuss specific trials you've managed and the outcomes, as this will demonstrate your expertise in the field.
✨Emphasise Compliance Experience
Since the role requires a strong grasp of GCP, ICH guidelines, and regulatory requirements, be ready to provide examples of how you've ensured compliance in past projects. Discuss any challenges you faced and how you overcame them.
✨Demonstrate Leadership Skills
As a Senior Clinical Trial Manager, you'll likely oversee other team members. Share experiences where you've successfully led a team or project, focusing on how you motivated others and ensured deliverables were met on time.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and ability to handle unexpected issues during trials. Think of specific scenarios from your past work where you had to identify risks and implement corrective actions effectively.
