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- Tasks: Lead and design clinical studies in hematology/oncology, collaborating with diverse teams.
- Company: Dynamic healthcare organisation focused on innovative cancer treatments.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Make a real impact in cancer research while working with top professionals.
- Qualifications: MS required; PhD, PharmD, or MD preferred with 5+ years of relevant experience.
- Other info: Join a collaborative environment in London with excellent career advancement opportunities.
The predicted salary is between 43200 - 72000 £ per year.
The Senior Director, Clinical Scientist is responsible for leading/contributing to study design and execution of clinical studies in hematology/oncology. As a leader within the clinical organization, this individual will be partnering with clinical operations, translational, and other matrix team members to design and refine clinical plans, author key clinical/regulatory documents, and ensure exceptional delivery and interpretation of clinical data. The Director will strive to drive study enrollment, build and maintain collaborative relationships with investigators and clinical site staff, CROs, and colleagues. The Director will foster a proactive and thoughtful approach to clinical study execution where obstacles are anticipated and effectively mitigated/resolved.
Responsibilities
- Leads/Contributes to study design and amendments in collaboration with internal and external scientific stakeholders.
- Collaborates with MD, regulatory and other internal partners/stakeholders for authoring and submission of protocols, protocol amendments, regulatory filings, and other regulatory documentation.
- Collaborates with clinical operations, data management and CRO to develop and implement the overall data quality plan and leads internal medical data review and safety trend analysis on one or more studies/programs.
- Point-of-contact for clinical inquiries from CRO medical monitor and other stakeholders.
- Develops and provides input for clinical presentation slides and other materials for internal/external meetings and/or ongoing communications.
- Partners with clinical operations and CRO in developing and maintaining study start-up documents/resources (e.g., ICF, Lab Manual, EDC, Safety monitoring Plan).
- Participates in safety meetings and tracks, analyzes, and reviews documentation for any potential safety events.
- Leads/Contributes to development and implementation of communications strategies to support existing and concluded studies, including KOL interactions, advisory boards, major medical meetings, congresses and other events, publications and other materials.
- Writes and/or reviews abstracts, posters, content for scientific meetings, conferences, other events and presentations, and coordinates further reviews with internal partners and stakeholders.
- Coordinates submissions to scientific meetings and/or other appropriate venues or groups.
- Writes clinical science sections of meeting packages and assists in the development and review of other clinical documentation required for regulatory submissions.
- All other duties as assigned.
Qualifications
- MS (or equivalent) required.
- PhD, PharmD, or MD preferred.
- 5+ years overall related experience with PhD or similar degree; Minimum of 2 years' experience in conducting/supporting oncology/hematology clinical studies.
- Excellent written and verbal communication skills.
- Expertise in interpreting immunology/immuno-oncology translational data in addition to clinical data.
Location: London, England, United Kingdom
Senior Director, Clinical Scientist in London employer: Summit Therapeutics, Inc.
Contact Detail:
Summit Therapeutics, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Director, Clinical Scientist in London
✨Network Like a Pro
Get out there and connect with people in the industry! Attend conferences, seminars, or even local meet-ups. Building relationships with professionals in hematology/oncology can open doors to opportunities that aren’t advertised.
✨Showcase Your Expertise
When you get the chance to chat with potential employers, don’t hold back on sharing your knowledge. Discuss your experience with clinical studies and how you've tackled challenges in the past. This will help you stand out as a candidate who can drive study enrollment and collaborate effectively.
✨Prepare for Interviews
Research the company and its recent projects in clinical science. Be ready to discuss how your background aligns with their goals, especially in study design and execution. Practising common interview questions can also boost your confidence!
✨Apply Through Our Website
Don’t forget to check out our website for job openings! Applying directly through us not only shows your interest but also gives you a better chance of being noticed by our hiring team. Let’s get you that Senior Director role!
We think you need these skills to ace Senior Director, Clinical Scientist in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Director, Clinical Scientist role. Highlight your experience in hematology/oncology and any leadership roles you've held. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical studies and how you can contribute to our team. Be sure to mention specific experiences that relate to the responsibilities listed in the job description.
Showcase Your Communication Skills: Since excellent written communication is key for this role, make sure your application is clear and concise. We love a well-structured application that reflects your ability to communicate complex ideas effectively.
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 shows you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at Summit Therapeutics, Inc.
✨Know Your Stuff
Make sure you’re well-versed in the latest trends and developments in hematology and oncology. Brush up on recent studies, clinical trial designs, and regulatory requirements. This will not only show your expertise but also demonstrate your genuine interest in the field.
✨Showcase Your Leadership Skills
As a Senior Director, you'll need to lead teams and collaborate with various stakeholders. Prepare examples of how you've successfully led projects or teams in the past. Highlight your ability to build relationships and navigate challenges in clinical study execution.
✨Prepare for Technical Questions
Expect questions that dive deep into your experience with clinical study design and data interpretation. Be ready to discuss specific methodologies you've used, how you've handled safety events, and your approach to ensuring data quality. Use real-life scenarios to illustrate your points.
✨Communicate Clearly and Confidently
Your communication skills are crucial for this role. Practice articulating complex scientific concepts in a clear and concise manner. During the interview, make sure to engage with your interviewers, ask questions, and express your thoughts confidently to leave a lasting impression.
