Senior Clinical Trial Leader

Novartis; London; Hybrid; GBP 60,000 - 90,000; Full time

Job summary

A leading company in the pharmaceutical sector seeks a Senior Clinical Sciences Trial Leader to drive the planning and execution of translational medicine trials. You will leverage your expertise in clinical science to ensure trials are conducted with high standards, collaborating with international teams to foster innovation in patient-centric designs.

Qualifications

• 4+ years’ experience in clinical trial management/operations.
• Demonstrated leadership experience and interpersonal skills.
• Strong project management experience with multiple priorities.

Responsibilities

• Lead operational aspects of clinical studies and trial execution.
• Drive the development of clinical study protocols.
• Collaborate with global teams and mentor junior members.

Skills

Budget Management

Clinical Research

Clinical Trial Protocol

Clinical Trials

Coaching

Data Analysis

Data Integrity

Learning Design

Lifesciences

Risk Monitoring

Trends Analysis

Education

PhD or PharmD in life sciences

BSc or MSc in life sciences

Job description

Job Description Summary
LI#Hybrid

This position is based at the Westworks London office, with flexibility to work remotely two days a week. This position may require up to 5% travel as defined by the business.

We are Clinical Sciences and Innovation at Novartis. A dynamic group of Clinical Scientists who plan and execute early phase trials worldwide. From First-in-Human to Proof-of-Concept and beyond. We design and operationalize trials, ensuring they run smoothly, on time and - most importantly - with patients' interests to the fore.

Curious, unbossed and inspired; we are committed to flexibility in the workplace.

Job Description

As a Senior Clinical Sciences Trial Leader, you will lead the clinical science and operations of planning and executing translational medicine clinical trials. Collaborate across our global network and partner with outstanding physicians and scientists. By building your therapeutic area expertise, you will deliver next-generation, digital and patient-centric trial designs. Being always curious, innovative and inspiring.

More specifically, you will:
• Operationally and scientifically lead complex clinical studies.
• Drive and deliver aspects of global clinical trial execution from study design, set-up and recruitment to final reporting.
• Lead the matrix-management of robust global clinical trial teams, collaborating across the organization and externally with service providers/investigator sites.
• Drive the development of clinical study protocols, clinical operations execution plans and other required documents.
• Ensure quality conduct and document standards are applied across the clinical trial lifecycle.
• Lead or support clinical data review
• Contribute to project/program level plans

• May mentor junior team members as required.
• Support optimization of standard methodologies in clinical trial operations and adopt an open learning and sharing environment.
• Unleash the value of data and digital within clinical studies.

Ultimately, YOU will help bring new technologies and therapies closer to our patients.

Minimum requirements :

• In this role, you will bring:
  • A life sciences PhD or PharmD (desirable), or BSc or MSc in life sciences.
  • 4+ years' experience in clinical trial management/operations, coupled with a broad knowledge of the drug development field; preferably within the pharma industry.
• Demonstrated leadership experience and well-developed interpersonal skills.
• A track record of collaborating with and influencing a wide range of people, and of building strong partnerships, inspiring mutual respect and fostering a positive, inclusive team culture.
• Strong project management experience; excellent planning, prioritization and organizational skills; used to managing multiple priorities concurrently.
• Strong scientific and clinical expertise with the ability to interpret and represent trial-level data, while maintaining a patient-centric mindset that integrates patient insights into protocol development, trial planning, and execution.
• High change agility, thriving in an open and dynamic environment. Able to learn proactively, tackle issues and take accountability.
• Clear written and verbal expression of ideas; an active communicator.

Final job title and associated responsibilities will be commensurate with the successful candidates' level of expertise.

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. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

You'll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards

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.

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network

Skills Desired
Budget Management, Clinical Research, Clinical Trial Protocol, Clinical Trials, Coaching, Data Analysis, Data Integrity, Learning Design, Lifesciences, Risk Monitoring, Trends Analysis