(Senior) Director Clinical Development in Cambridge

(Senior) Director Clinical Development in Cambridge

Cambridge Full-Time 72000 - 108000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead clinical development strategy and design impactful clinical trials for innovative therapies.
  • Company: Join a pioneering pharmaceutical company dedicated to improving patient outcomes.
  • Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
  • Why this job: Make a real difference in healthcare by shaping the future of clinical development.
  • Qualifications: Medical degree with extensive experience in clinical development and regulatory interactions.
  • Other info: Collaborative environment with a focus on innovation and patient care.

The predicted salary is between 72000 - 108000 £ per year.

The (Senior) Director Clinical Development is responsible for shaping, developing and executing the clinical development strategy for the assigned product. Specific responsibilities include:

  • Design of clinical trials (any phase as required by the clinical development program, including phase IV).
  • Clinical protocol development.
  • Medical monitoring of clinical trials.
  • Analysis of study data.
  • Contribution and review of clinical study reports, clinical modules of registration dossiers, and briefing books for interactions with Health Authorities.

The (Senior) Director Clinical Development will represent and defend the clinical strategy during MAA regulatory review processes across multiple geographies and in meetings with Health Authorities. The individual will closely work with other RD functions to ensure the successful progress of projects and clinical trials and will interact with the scientific and patient community to ensure their insights are adequately incorporated in the clinical trials. This position will require representing Sobi clinical development strategy externally as well as in internal meetings with senior management if required.

Essential to success is a strong clinical development background with previous experience in late-stage clinical trial design and conduct and in major regulatory submission (e.g., EU, Canada, Japan); excellent medical knowledge in lipidology and cardiovascular; ability to build and maintain strong relationships with study investigators/KOLs; and ability to collaborate cross-functionally.

Responsibilities include, but are not limited to:

  • Shape and develop the clinical development plans, while adhering to the highest scientific and ethical standards.
  • Design, conduct and report Sobi-sponsored studies in close collaboration with the rest of the clinical development team, the clinical study teams, regulatory, safety and other cross-functional teams, as applicable.
  • Act as Study Physician responsible for Sobi-sponsored studies if required: responsible for the development of clinical study synopsis and protocols, contribute to the statistical analysis plans, perform medical monitoring, participate in Investigator meetings and other study-related activities and provide input/review of other main clinical study documents, as needed and appropriate.
  • Interact and consult with key opinion leaders and patient representatives, and lead advisory boards to define the clinical development strategy and inform the clinical trial design.
  • Provide strategic and operational clinical development expertise in interactions with regulatory and reimbursement authorities.
  • Contribute with high-quality scientific and medical input to delivery of clinical parts of submissions and other regulatory documents as well as to responses to Health Authority’s questions to support e.g., scientific advice, IND application, marketing authorization across multiple geographies.
  • Represent the clinical function in meetings with Health Authorities.
  • Where applicable and assigned, provide scientific and medical expert support to other functions within Sobi on specific therapeutic area of expertise, including global safety, medical affairs activities such as advisory boards, scientific communications & publications, and business development such as due diligence evaluations of external compounds and M&A.

Qualifications:

  • Medical Degree Specialty in cardiology, lipidology, endocrinology or relevant previous clinical development experience (+7 years) in these therapeutic areas.
  • Relevant global clinical development experience in the Pharmaceutical Industry (+10 years).
  • Previous experience in interactions with major Health Authorities.
  • Solid record of accomplishment in drug development programs within the relevant therapeutic area demonstrating outstanding and intimate understanding of translating early stage programs into the clinic and further across the clinical development chain.
  • Expertise in bringing the medical and scientific perspective, drug development wisdom to business development, corporate strategy and leadership decision making.
  • Demonstrated ability to build and execute strategic and tactical development and medical plans.
  • Experience and ability to engage with key internal and external stakeholders.

Highly Desired:

  • At least 5 years clinical experience in treating patients.
  • Successful interactions with major Health Authorities leading to drug approvals.

Skills/Languages Required:

  • Excellent communication skills, capable of representing the company to all audiences both internally and externally.
  • Strategic mindset.
  • Excellent organizational skills, be a self-motivated driver of best practices and processes in the management of projects and operations.
  • Excellent written and verbal communication skills in English.
  • Able to demonstrate behaviours in line with Sobi’s core values: Care, Ambition, Urgency, Ownership and Partnership.

Personal Attributes Required:

  • Good team-player, able to work effectively in a team setting and interact respectfully with people of different cultural, seniority and functional backgrounds.
  • Highly flexible and comfortable working in a fast-paced and quickly changing environment.
  • Able to work well in a virtual environment.
  • Proven self-management by showing initiative, good organization and willingness to be held accountable.
  • Results oriented with a can-do and proactive attitude.
  • High medical, scientific and ethical integrity.
  • Able to prioritise.

Additional Information:

  • Driven, flexible and with strong team working and project management skills.
  • Strong interpersonal, cultural and communication skills.
  • Analytical, with a problem-solving and collaborative mindset.
  • Forward looking mindset, to ensure that our PV ESP systems and operations environment is being continuously developed to ensure ongoing compliance and to deliver high quality and cost-effective outcomes.
  • Strong ability to work independently and to make priorities in order to deliver business critical items in time.
  • Demonstrate the Sobi Values: Care for our patients, for our colleagues and for our company, Ambition, Urgency, Ownership and Partnership.

(Senior) Director Clinical Development in Cambridge employer: Sobi - Swedish Orphan Biovitrum AB (publ)

Sobi is an exceptional employer that prioritises the growth and development of its employees, offering a dynamic work culture that fosters collaboration and innovation in the pharmaceutical industry. With a strong commitment to scientific integrity and ethical standards, Sobi provides unique opportunities for professionals to engage with key opinion leaders and health authorities, ensuring that their contributions have a meaningful impact on patient care. Located in a vibrant area, Sobi encourages a flexible work environment that supports work-life balance while driving ambitious projects in clinical development.
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Contact Detail:

Sobi - Swedish Orphan Biovitrum AB (publ) Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land (Senior) Director Clinical Development in Cambridge

✨Tip Number 1

Network like a pro! Reach out to your connections in the clinical development field, especially those who have experience with regulatory submissions. A friendly chat can lead to insider info about job openings or even a referral.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of lipidology and cardiovascular medicine. Be ready to discuss how your past experiences align with the responsibilities of the (Senior) Director Clinical Development role.

✨Tip Number 3

Showcase your strategic mindset during interviews. Talk about specific examples where you’ve successfully shaped clinical development plans or navigated complex regulatory environments. This will demonstrate your fit for the role.

✨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 Development in Cambridge

Clinical Development Strategy
Clinical Trial Design
Medical Monitoring
Data Analysis
Regulatory Submission Expertise
Lipidology Knowledge
Cardiovascular Expertise
Stakeholder Engagement
Cross-Functional Collaboration
Communication Skills
Project Management
Strategic Mindset
Organisational Skills
Problem-Solving Skills
Teamwork

Some tips for your application 🫡

Tailor Your Application: Make sure to customise your CV and cover letter to highlight your experience in clinical development, especially in late-stage trials. We want to see how your background aligns with the specific responsibilities mentioned in the job description.

Showcase Your Expertise: Don’t hold back on showcasing your medical knowledge in lipidology and cardiovascular areas. We’re looking for someone who can bring that expertise to the table, so make it clear how your skills can contribute to our clinical development strategy.

Highlight Collaboration Skills: Since this role involves working closely with various teams and stakeholders, emphasise your ability to collaborate cross-functionally. Share examples of how you’ve successfully built relationships with key opinion leaders or worked with regulatory authorities.

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 your initiative and interest in joining our team!

How to prepare for a job interview at Sobi - Swedish Orphan Biovitrum AB (publ)

✨Know Your Clinical Development Inside Out

Make sure you have a solid grasp of clinical development strategies, especially in lipidology and cardiovascular areas. Brush up on your knowledge of late-stage clinical trial design and major regulatory submissions, as these will be key topics during your interview.

✨Prepare for Regulatory Discussions

Since you'll be representing the clinical strategy in front of Health Authorities, it’s crucial to prepare for questions related to regulatory processes. Familiarise yourself with the MAA review process and be ready to discuss how you've successfully navigated similar situations in the past.

✨Showcase Your Collaborative Spirit

This role requires strong cross-functional collaboration. Be prepared to share examples of how you've worked effectively with diverse teams, including clinical study teams and external stakeholders like KOLs. Highlight your ability to build relationships and drive projects forward.

✨Demonstrate Your Strategic Mindset

The interviewers will be looking for your ability to think strategically about clinical development. Prepare to discuss how you've shaped clinical development plans in previous roles and how you align them with business objectives. Show that you can balance scientific integrity with practical execution.

(Senior) Director Clinical Development in Cambridge
Sobi - Swedish Orphan Biovitrum AB (publ)
Location: Cambridge
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