Clinical Sciences Trial Leader in London

Clinical Sciences Trial Leader in London

London Full-Time 51750 - 63250 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead global clinical trial teams and ensure high-quality research data delivery.
  • Company: Join Novartis, a leader in innovative medicine with a mission to improve lives.
  • Benefits: Enjoy a competitive salary, hybrid work model, and opportunities for professional growth.
  • Other info: Dynamic work environment with a focus on collaboration and diversity.
  • Why this job: Make a real impact in healthcare by leading groundbreaking clinical trials.
  • Qualifications: Bachelor's in life sciences; 2+ years in clinical trials preferred.

The predicted salary is between 51750 - 63250 £ per year.

As a Clinical Trial Leader, you will be leading the global multidisciplinary matrix Clinical Trial Team (CTT) to ensure all trial deliverables are met. You will be responsible for the availability of high quality, Biomedical Research data according to agreed timelines and budget to enable no delays in strategic decision making and drug registration.

This is a hybrid role – there is a requirement to be on site in the Westworks London office three days a week. We are unable to offer permit support for this role. We have the option to hire someone at Senior Clinical Trial Leader if this role level is a better match to the experience and skill set of the applicant.

Major accountabilities:

  • Study Leader and/or Clinical Scientist for predominantly low complexity, global studies and may provide additional Clinical Sciences support to high complexity, global studies.
  • Lead or support the clinical protocol development process in collaboration with the Medical Lead and other line functions; responsible author for clinical protocols, amendments, etc.; contribute to the medical/scientific input given for the development of study-related documents and processes which resides in other line functions; contribute to the development of clinical sections of study-level regulatory documents.
  • Support development of strategic and scientific input into study concept, feasibility, and ability to execute; develops and implements study-level operational execution plan in partnership with key cross functional partners, if applicable.
  • Collaborate with key cross functional partners to identify and select strategic and high performing sites to ensure recruitment commitments are met.
  • Lead or support a global cross functional CTT to ensure all trial deliverables are met; sets stretch goals, promotes realistic planning and timelines, and presents actionable alternatives to accelerate timelines.
  • Partner with line functions to gain input and alignment and manages internal and external stakeholder expectations.
  • Lead or support the ongoing medical/scientific review of clinical trial data across assigned studies in collaboration with the medical expert and key line functions, and partners on data analysis and data interpretation, including safety trend analysis, signal detection, development of first interpretable results, reporting clinical study results in CSR, and internal/external publications.
  • Prepare, lead or support dose escalation meetings with investigators.
  • Coordinate the real time availability of quality clinical trial data, to provide consolidated information for dose escalation meetings and Phase II data reviews with relevant stakeholders.

Minimum Requirements:

  • Bachelors in life science/healthcare required; Advanced degree or equivalent education/degree in life sciences/healthcare preferred (PhD/MD/PharmD/Masters).
  • Approximately 2+ years’ experience in clinical trials/development.
  • Fluent English (oral and written).
  • For TCO: Strong understanding of oncology/hematology and demonstrates high learning agility.
  • For TM: Demonstrates high learning agility.
  • Demonstrated ability to drive collaborations through unpredictable circumstances and higher paced changes.
  • Demonstrates leadership and influence by creating a positive work environment by inspiring and encouraging mutual respect.

Why Novartis?

Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us!

Accessibility & Accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to us and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Clinical Sciences Trial Leader in London employer: Novartis Farmacéutica

At Novartis, we pride ourselves on being an exceptional employer, particularly for the role of Director: AI Systems Reliability, Testing & Performance in London. Our collaborative work culture fosters innovation and continuous learning, providing employees with ample opportunities for professional growth and development in the rapidly evolving field of AI. With a commitment to excellence and a focus on meaningful contributions to healthcare, Novartis offers a unique environment where your expertise can make a significant impact.

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Contact Details:

Novartis Farmacéutica Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Clinical Sciences Trial Leader in London

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We think you need these skills to ace Clinical Sciences Trial Leader in London

Communication Skills
Problem-Solving Skills
Compassion
Flexibility
Organizational Skills
Teamwork
Adaptability

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Novartis Farmacéutica!

Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Novartis Farmacéutica that you're not just a fit for the job but also a safety-conscious candidate!

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How to prepare for a job interview at Novartis Farmacéutica

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Novartis Farmacéutica that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

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