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For Companies At a Glance
- Tasks: Lead clinical trial strategies and collaborate across teams to drive oncology research.
- Company: Join Sanofi, a pioneering biopharma company focused on innovative healthcare solutions.
- Benefits: Enjoy competitive salary, extensive health benefits, and generous parental leave.
- Why this job: Make a real impact in oncology research and improve lives through groundbreaking science.
- Qualifications: MD or equivalent with experience in clinical development and oncology preferred.
- Other info: Dynamic, inclusive workplace with opportunities for international career growth.
Location: Cambridge, MA, Morristown, NJ
About the Job
Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions. As a Senior Clinical Research Director (Senior CRD) within the Oncology Therapeutic Area, you will lead the clinical trial strategy for one or more multiple myeloma assets, creating synergies across Clinical Operations, Biostatistics, Regulatory, Translational Medicine, Project Management, New Product Planning and Pharmacovigilance to establish the development strategy and execute the development plan.
About Sanofi: We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
Main Responsibilities
- Working within a matrix model, establish or adapt clinical development and contingency plans by engaging with clinical investigators, advisors and regulatory authorities.
- Author protocols, extended synopses, clinical sections of the Investigator Brochure, IND/IMPD fillings, annual reports, development risk management plans.
- Lead the clinical interpretation of study results.
- Contribute to clinical study reports and clinical summaries, including regulatory submissions.
- Provide expert medical guidance to other functions, including Clinical Operations, Biostatistics and Translational Medicine, to ensure optimal planning and execution of clinical trials.
- Present and discuss development strategy and clinical study results with key internal stakeholders, external investigators, advisory boards, and regulatory authorities.
- Author clinical abstracts, presentations for conferences, and manuscripts.
About You
Education
- Medical Doctor (MD) or equivalent; training in Oncology and/or Hematology, preferably with experience in myeloma or hematologic malignancies is a plus.
Experience
- At least 4 years experience in clinical development in the pharmaceutical industry, CRO, or healthcare institution.
Soft skills
- Excellent communication skills (verbal and written English) with both internal and external stakeholders.
- Adept at problem solving.
- Thoughtful risk-taking: challenge decisions and status quo with a risk-management approach.
- Demonstrated ability to work with a multi-functional team to achieve project milestones.
- Understanding of and willingness to meet applicable regulatory, quality and compliance standards.
- Quality-focused, adept at developing good practices, open-minded to data-driven approaches and new digital solutions.
- International/intercultural working skills.
Preferred location is Cambridge, MA. Morristown, NJ and Vitry, France considered.
Why Choose Us?
- Bring the miracles of science to life alongside a supportive, future-focused team.
- Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
- Enjoy a thoughtful, well-crafted rewards package that recognises your contribution and amplifies your impact.
- Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; colour; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
The salary range for this position is: $236,250.00 - $393,750.00. All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs.
Senior Clinical Research Director - Oncology in Cambridge employer: Sanofi
Contact Detail:
Sanofi Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Director - Oncology in Cambridge
✨Tip Number 1
Network like a pro! Reach out to your connections in the oncology field, attend relevant conferences, and engage with professionals on LinkedIn. The more people you know, the better your chances of landing that Senior Clinical Research Director role.
✨Tip Number 2
Prepare for interviews by brushing up on your clinical trial strategies and recent advancements in oncology. Be ready to discuss how you can contribute to Sanofi’s mission and drive breakthroughs in cancer treatment. Show them you’re not just a fit, but the perfect fit!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After interviews or networking events, send a quick thank-you note to express your appreciation and reiterate your interest in the position. It keeps you top of mind and shows your enthusiasm.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in being part of our team at Sanofi. Let’s make those miracles happen together!
We think you need these skills to ace Senior Clinical Research Director - Oncology in Cambridge
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Senior Clinical Research Director role. Highlight your experience in oncology and clinical development, and show how your skills align with our mission at Sanofi.
Showcase Your Communication Skills: Since excellent communication is key for this role, use clear and concise language in your application. Don’t forget to demonstrate your ability to engage with both internal teams and external stakeholders.
Highlight Problem-Solving Abilities: We love candidates who can think on their feet! Share examples of how you've tackled challenges in previous roles, especially in clinical research or multi-functional team settings.
Apply Through Our Website: For the best chance of success, make sure to submit your application through our official website. This way, we can easily track your application and get back to you quicker!
How to prepare for a job interview at Sanofi
✨Know Your Oncology Stuff
Make sure you brush up on the latest developments in oncology, especially around multiple myeloma. Familiarise yourself with recent studies and breakthroughs that could be relevant to the role. This will not only show your passion but also your commitment to staying updated in the field.
✨Master the Matrix Model
Since the role involves working within a matrix model, be prepared to discuss how you've successfully collaborated across different functions in previous roles. Think of specific examples where you led or contributed to cross-functional teams, and be ready to explain your approach to problem-solving in those situations.
✨Prepare for Regulatory Discussions
Given the importance of regulatory compliance in this position, review key regulations and guidelines related to clinical trials. Be ready to discuss how you've navigated regulatory challenges in the past and how you would approach them in this role. This shows you understand the landscape and can handle the complexities involved.
✨Showcase Your Communication Skills
Excellent communication is crucial for this role, so practice articulating your thoughts clearly and concisely. Prepare to discuss how you've effectively communicated complex information to both technical and non-technical stakeholders. Consider using the STAR method (Situation, Task, Action, Result) to structure your responses.
