At a Glance
- Tasks: Lead innovative clinical programs in biotech, ensuring patient safety and scientific integrity.
- Company: Join a cutting-edge biotech firm making strides in cell and gene therapy.
- Benefits: Competitive salary, comprehensive health benefits, and opportunities for professional growth.
- Other info: Dynamic role with strong potential for career advancement in a thriving environment.
- Why this job: Make a real impact in drug development and collaborate with top industry experts.
- Qualifications: MD or equivalent with 10 years of experience in clinical development.
The predicted salary is between 100000 - 150000 £ per year.
ARTO is again working with an innovative biotech company who are looking to progress their lead program through the clinic. With already strong data, they are looking for an experienced Clinical Development Physician to drive this program.
About the job:
- Provide strategic and operational medical leadership for Phase I and II clinical programs across cell and gene therapy/immunology portfolios, ensuring scientific integrity and patient safety throughout development.
- Lead end-to-end clinical development activities including protocol design, study execution, data interpretation, regulatory interactions, and clinical study reporting.
- Serve as the medical lead for early-stage clinical trials, overseeing dose escalation strategies, safety review committees, and benefit-risk assessments.
- Collaborate cross-functionally with Clinical Operations, Translational Sciences, Regulatory Affairs, Biometrics, and CMC teams to drive program milestones and development plans.
- Contribute to clinical development strategy, target product profiles, and lifecycle planning aligned with corporate and portfolio objectives.
- Build and maintain strong relationships with investigators, key opinion leaders, academic collaborators, and external partners within the biotechnology ecosystem.
- Support global regulatory submissions and interactions with agencies including the FDA, EMA, and MHRA, ensuring compliance with GCP and applicable regulatory standards.
Qualifications:
- MD or equivalent medical degree, PharmD, or PhD in a clinical and/or scientific discipline.
- Clinical background or sufficient industry experience within Rheumatology/Immunology.
- A proven leader with roughly 10 years pharmaceutical/biotechnology industry experience in all phases of drug development.
- Deep knowledge of the drug development process with a focus on clinical study design and management; ability to collaborate with, support, and oversee CROs.
- Able to drive strategic thinking and plans for successful clinical trial outcomes.
- Experience interfacing with the global regulatory authorities (incl. FDA, EMA) and respective standards, including hands-on experience in global drug development.
- Recent experience of IND and NDA/BLA submissions strongly preferred.
- Dynamic individual with excellent written, communication, and interpersonal skills.
If you'd like to talk through this further, please reach out via the below email address.
Senior/Execuitve Medical Director - Clinical Development in Slough employer: ARTO
Join an innovative biotech company that prioritises scientific integrity and patient safety while fostering a collaborative work culture. With a strong focus on employee growth, this organisation offers unique opportunities to lead cutting-edge clinical development programmes in a dynamic environment, ensuring your contributions directly impact the future of healthcare. Located in a vibrant area, employees enjoy a supportive atmosphere that encourages professional development and meaningful engagement with industry leaders.
StudySmarter Expert Advice🤫
We think this is how you could land Senior/Execuitve Medical Director - Clinical Development in Slough
✨Tip Number 1
Network like a pro! Reach out to your connections in the biotech field, especially those who have experience in clinical development. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of the latest trends in cell and gene therapy. We want you to showcase your expertise and passion for the industry, so be ready to discuss how you can contribute to their innovative projects.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation. It keeps you fresh in their minds and shows your enthusiasm for the role.
✨Tip Number 4
Apply directly 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 joining our team and making an impact in clinical development.
We think you need these skills to ace Senior/Execuitve Medical Director - Clinical Development in Slough
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to highlight your experience in clinical development, especially in areas like cell and gene therapy. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about this role and how your skills can drive our clinical programs forward. Keep it concise but impactful – we love a good story!
Showcase Your Leadership Skills:As a Senior/Executive Medical Director, leadership is key. In your application, highlight specific examples where you've led teams or projects successfully. We want to know how you can inspire and guide others in our innovative environment.
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 ARTO
✨Know Your Clinical Development Inside Out
Make sure you brush up on your knowledge of clinical development, especially in relation to Phase I and II trials. Be prepared to discuss specific protocols you've designed or led, and how you've ensured patient safety and scientific integrity in your past roles.
✨Showcase Your Leadership Skills
As a Senior/Executive Medical Director, leadership is key. Think of examples where you've successfully led cross-functional teams or managed complex projects. Highlight your ability to drive strategic thinking and how you've navigated challenges in the drug development process.
✨Familiarise Yourself with Regulatory Standards
Since this role involves interactions with global regulatory authorities, make sure you're up to speed on GCP and the latest regulations from the FDA, EMA, and MHRA. Be ready to discuss your experience with IND and NDA/BLA submissions, as well as any direct interactions you've had with these agencies.
✨Build Rapport with Key Opinion Leaders
Demonstrate your ability to build and maintain relationships within the biotechnology ecosystem. Prepare to talk about your collaborations with investigators and academic partners, and how these relationships have contributed to successful clinical outcomes in your previous roles.
