At a Glance
- Tasks: Lead global clinical studies in non-obstructive respiratory diseases and ensure scientific integrity.
- Company: Join a dynamic, fast-growing pharmaceutical company that values its people.
- Benefits: Flexible working, remote options, continuous training, and a focus on work-life balance.
- Why this job: Make a real impact in respiratory health while collaborating with top experts.
- Qualifications: Medical Doctor degree and 5+ years in the pharmaceutical industry preferred.
- Other info: Enjoy a friendly environment with excellent career development opportunities.
The predicted salary is between 36000 - 60000 £ per year.
The Senior Clinical Research Physician provides scientific and strategic leadership in the design, execution, and interpretation of global clinical studies in the non-obstructive respiratory diseases therapeutic area. They drive the preparation of documents for regulatory submissions, ensuring the scientific validity and rigor of key documents, including study protocols, investigator brochures, and clinical study reports. They are able to work comfortably in a matrix environment and are an integral member of the cross-functional clinical study team. They use therapeutic expertise to ensure incorporation of robust scientific principles into study design and conduct and to enhance competencies across R&D.
Main Responsibilities
- Enhances clinical study execution, working cross-functionally with internal stakeholders and the Clinical team to uphold medical and scientific integrity across clinical trials.
- Drive medical and scientific input into clinical trial design and execution in accordance with the Clinical Development Plan and related key clinical documentation (e.g. clinical section of the Investigator's Brochure, Protocols and Clinical Study Reports).
- Conduct ongoing medical and scientific review of clinical trial data, ensuring data integrity, patient safety and the ongoing benefit-risk assessment.
- Responsible for the clinical interpretation of study data and communication to internal and external stakeholders.
- Ensure the safeguard of Patient Safety: in collaboration with and in support of Corporate Pharmacovigilance identify safety signals, review narratives, take actions with investigators when Serious/unexpected Adverse Events are reported.
- Represent the company in front of health authorities, regulatory agencies, external partners, and scientific institutions, contributing to regulatory discussions and ensuring alignment with Global Clinical Development objectives.
- Collaborate with Clinical Program Leaders, statisticians, regulatory affairs, and other key functions to drive clinical development plans and contribute to regulatory submission documentation.
- Engage with external experts, regulatory bodies, ethics committees, investigators, and safety monitoring committees to ensure alignment with scientific and medical needs.
- Be delegated to replace CPL or be assigned as CPL for some specific phase of the clinical programs.
- Provide medical and scientific inputs in RWE studies/disease registries.
Experience Required
- At least 5 years in the pharmaceutical industry preferred, although equivalent expertise in clinical or academic research will be considered, preferably within the Respiratory or Allergy & Immunology therapeutic areas.
- Experience within the specific therapeutic area (Interstitial Lung Disease; Pulmonary Hypertension) and experience in pharmaceutical/biotech industry are preferred and will be a plus.
Education
- Medical Doctor Degree from a recognised institution; certification in Pulmonary or Allergy & Immunology considered an advantage.
Languages
- Fluency in spoken and written English.
Technical Skills
- Excellent writing skills in order to effectively contribute to study documentation and reports.
- Outstanding communication skills with ability to interact with all internal stakeholders and external academic and regulatory experts.
- Strong understanding of GCP, regulatory requirements, and clinical trial methodologies.
- Ability to interpret and effectively communicate complex clinical and scientific data, and literature.
What we offer
You would join a dynamic, fast-growing, challenging and friendly environment. In Chiesi we firmly believe that our people are our most valuable asset, that is why we invest in continuous training, learning and development. Therefore, we strive to continuously promote and satisfy development needs, paying particular attention to the quality of our working environment and to collective well-being. We want our people to come to work happy every day, and we know how important it is to find the right work-life balance in order to be able to give our best. That is why we offer flexible working approach, remote working, support in the relocation process, tax assistance service for foreign colleagues and many other people-care services.
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases in London employer: Chiesi Group
Contact Detail:
Chiesi Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Physician Non-Obstructive Respiratory Diseases in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the respiratory field on LinkedIn or at industry events. A friendly chat can lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by diving deep into the latest research and trends in non-obstructive respiratory diseases. Show us you’re not just knowledgeable but passionate about the field!
✨Tip Number 3
Practice your communication skills! You’ll need to explain complex clinical data clearly, so grab a friend and do some mock interviews. The more you practice, the more confident you’ll feel.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive!
We think you need these skills to ace Senior Clinical Research Physician Non-Obstructive Respiratory Diseases in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences that align with the Senior Clinical Research Physician role. Highlight your expertise in non-obstructive respiratory diseases and any relevant clinical trial experience to catch our eye!
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 background makes you the perfect fit. Don’t forget to mention your understanding of GCP and regulatory requirements.
Showcase Your Communication Skills: Since this role involves interacting with various stakeholders, demonstrate your outstanding communication skills in your application. Whether it's through your writing style or examples of past collaborations, let us see how you can engage effectively!
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Chiesi Group
✨Know Your Stuff
Make sure you brush up on the latest developments in non-obstructive respiratory diseases. Familiarise yourself with key studies and regulatory requirements, as well as the specific therapeutic areas mentioned in the job description. This will show your genuine interest and expertise during the interview.
✨Prepare for Scenario Questions
Expect to be asked about how you would handle specific situations related to clinical trial design and execution. Think of examples from your past experience where you demonstrated leadership, problem-solving, and collaboration in a cross-functional team. Be ready to discuss these scenarios in detail.
✨Showcase Your Communication Skills
Since the role involves interacting with various stakeholders, practice articulating complex clinical data clearly and concisely. You might be asked to explain a study protocol or a clinical report, so being able to communicate effectively is crucial. Consider doing mock interviews to refine this skill.
✨Ask Insightful Questions
At the end of the interview, have a few thoughtful questions prepared. Inquire about the company's approach to patient safety or how they integrate scientific input into their clinical development plans. This not only shows your enthusiasm but also helps you gauge if the company aligns with your values.