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- Tasks: Lead and design clinical studies in hematology/oncology, collaborating with diverse teams.
- Company: Join a pioneering organisation dedicated to advancing cancer research.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Make a significant impact in the fight against cancer while working with top experts.
- Qualifications: MS required; PhD, PharmD, or MD preferred with 5+ years of relevant experience.
- Other info: Dynamic role with excellent career advancement opportunities in a collaborative environment.
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. This individual will partner 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. A proactive and thoughtful approach to clinical study execution is essential, 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 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
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those in hematology/oncology. Attend industry events or webinars to meet potential collaborators and get your name out there.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of clinical study design and regulatory processes. Be ready to discuss your past experiences and how they relate to the role of Senior Director, Clinical Scientist.
✨Tip Number 3
Showcase your leadership skills! During interviews, highlight examples where you've successfully led teams or projects in clinical settings. This will demonstrate your ability to drive study enrollment and collaborate effectively.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Senior Director, Clinical Scientist
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 study design and execution, especially in hematology/oncology. 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 the perfect fit for this role. Share specific examples of your leadership in clinical studies and how you've collaborated with various teams. We love a good story!
Showcase Your Communication Skills: Since excellent written and verbal communication skills are key for this position, make sure your application reflects that. Keep your language clear and professional, and don’t forget to proofread for any typos or errors. We appreciate attention to detail!
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, key regulatory documents, and any relevant clinical data. This will not only show your expertise but also demonstrate your genuine interest in the field.
✨Collaborative Mindset
Since this role involves working closely with various teams, be prepared to discuss how you’ve successfully collaborated in the past. Think of specific examples where you’ve partnered with clinical operations or CROs to overcome challenges in study design or execution.
✨Communication is Key
As a Senior Director, you'll need to communicate complex information clearly. Practice articulating your thoughts on clinical plans and data interpretation. You might even want to prepare a few slides to showcase your ability to present data effectively during the interview.
✨Anticipate Challenges
Be ready to discuss potential obstacles in clinical study execution and how you would address them. Think about past experiences where you’ve had to mitigate risks or resolve issues proactively, and be prepared to share those insights.
