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For Companies At a Glance
- Tasks: Lead clinical trials and develop strategies to improve patient outcomes.
- Company: Join Novartis, a leader in innovative healthcare solutions.
- Benefits: Hybrid working, competitive salary, and opportunities for personal growth.
- Why this job: Make a real difference in patients' lives through groundbreaking research.
- Qualifications: Advanced degree in life sciences and experience in clinical research required.
- Other info: Diverse and inclusive workplace with a focus on collaboration.
The predicted salary is between 48000 - 72000 £ per year.
LOCATION: London, Dublin, Barcelona
ROLE TYPE: Hybrid Working
The Associate Clinical Development Director (Assoc. CDD) provides input to the development of protocols for assigned global clinical trials, scientific monitoring, and reporting of quality data. May be assigned to provide support to the development of the clinical and scientific strategy of assigned sections of a clinical development program, depending on the size and complexity.
About The Role
Major accountabilities:
- Provides input to the development of clinical development strategy, and contributes to the development of trial related documents (e.g., CTPs, informed consent form, case report forms, data monitoring committee charters, data analysis plan, reports, publications) for assigned clinical trial(s) consistent with Clinical Development Plan (CDP); develops materials for trial-related advisory boards, data monitoring committees, investigator meetings, and protocol training meetings for Novartis local clinical development teams.
- Provides clinical and scientific input and contributes to clinical sections of trial and program level regulatory documents (e.g., Investigator’s Brochures, Health Authority briefing books, safety updates, submission dossiers, and responses to Health Authorities).
- In collaboration with appropriate Clinical Trial Team (CTT) members: Ensures clinical development oversight and support of trials as needed.
- Conducts ongoing scientific review of clinical trial data with Clinical Scientific Expert(s) with appropriate oversight from Medical Lead/CDMD/CSL.
- Manages patient safety reports on trial data to safety and clinical boards (e.g., Safety Management Team (SMT), GCT, GPT) with appropriate oversight from Medical Lead/CDMD/CSL in collaboration with patient safety.
- Provides input into final analyses and interpretation including the development of the Clinical Study Report(s) (CSRs), publications and internal/external presentations, with appropriate oversight from Medical Lead/CDMD/CSL.
- Contributes to global initiatives (e.g., process improvement, training, SOP development, other Clinical Development line function initiatives).
- May be assigned to lead clinical trial(s) as Clinical Scientific Lead and provide leadership and guidance for all clinical aspects of a clinical trial in close collaboration with the assigned medical monitor and/or CDMD.
Education
Advanced degree in life sciences/healthcare (or clinically relevant degree) is required. PharmD, or PhD strongly preferred.
Languages: Fluent oral and written English
Experience/Professional Requirement
- ≥ 3 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV.
- ≥ 2 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in the pharmaceutical industry.
- Working knowledge of the assigned disease area is desired with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) or program level.
- Demonstrated ability to establish effective working relationships with stakeholders.
- Working knowledge of ICH, GCP, clinical trial design and methodology, statistics, and regulatory and clinical development processes.
- Strong communication skills, written and oral.
- Strong interpersonal skills.
- Strong negotiation and conflict resolution skills.
- People management preferred.
Commitment To Diversity And Inclusion
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Why Novartis
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?
Rewards
Learn about all the ways we’ll help you thrive personally and professionally.
Associate Clinical Development Director in London employer: Novartis
Contact Detail:
Novartis Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Clinical Development Director in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know that can land you that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. We recommend practising common interview questions and even role-playing with a friend. The more comfortable you are, the better you’ll shine when it’s your turn to impress!
✨Tip Number 3
Showcase your expertise! Bring along examples of your previous work or case studies that highlight your contributions to clinical trials. We want to see how you’ve made an impact in your past roles, so don’t hold back!
✨Tip Number 4
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 take the initiative to engage directly with us. Let’s make this happen together!
We think you need these skills to ace Associate Clinical Development Director in London
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Associate Clinical Development Director role. Highlight your relevant experience in clinical research and drug development, and don’t forget to mention any specific skills that match the job description.
Showcase Your Achievements: When detailing your experience, focus on your accomplishments in conducting clinical trials. Use metrics where possible to demonstrate your impact, like successful trial completions or improvements in data quality.
Be Clear and Concise: Keep your application clear and to the point. Use straightforward language and avoid jargon unless it’s relevant to the role. We want to see your qualifications without wading through unnecessary fluff!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team!
How to prepare for a job interview at Novartis
✨Know Your Protocols
Familiarise yourself with the clinical trial protocols and documents relevant to the role. Be prepared to discuss how you would contribute to developing these materials, as well as your understanding of the Clinical Development Plan.
✨Showcase Your Experience
Highlight your previous experience in clinical research or drug development, especially in Phases I through IV. Be ready to share specific examples of trials you've worked on, focusing on your contributions to planning, executing, and reporting.
✨Demonstrate Communication Skills
Since strong communication is key for this role, practice articulating complex scientific concepts clearly and concisely. Prepare to discuss how you've effectively communicated with stakeholders in past projects.
✨Emphasise Team Collaboration
This position requires collaboration with various teams. Be prepared to discuss how you've successfully worked within a team environment, managed conflicts, and built effective working relationships in your previous roles.
