Nonclinical Scientist

MS0160 GE Healthcare Limited; Chalfont St Giles; Sur place; GBP 60 000 - 90 000; Plein temps

Résumé du poste

GE HealthCare is seeking a Nonclinical Scientist to support the development of diagnostic imaging agents. This non-laboratory role combines scientific contributions with cross-functional teamwork and process improvement across the Nonclinical Development portfolio.

Reporting to the Global Head of Nonclinical Development, you will contribute biology, pharmacology and toxicology expertise, help prepare regulatory submissions and ensure high‑quality documentation and knowledge sharing.

Qualifications

• MSc or PhD in Biology, Pharmacology, Toxicology or Life Sciences or another relevant Life Science discipline.
• Experience and understanding in cardiology, neurology or oncology drug development.
• Imaging (PET, SPECT, CT, MR or ultrasound) is desired, but not essential.
• Experience with regulatory submissions and GLP safety studies is preferred, but not critical.
• High initiative, systematic and independent work, and strong English documentation.

Responsabilités

• Contribute scientific expertise in biology, pharmacology, toxicology or another life-science discipline to nonclinical development programmes.
• Support the effective operation of the Nonclinical Development team across multiple projects.
• Identify opportunities to simplify and improve team processes and ways of working.
• Contribute to continuous improvement initiatives within Nonclinical Development.
• Provide flexible scientific and operational support across the portfolio according to changing priorities.
• Support design, planning, conduct and interpretation of nonclinical studies (in vitro/in vivo).
• Take responsibility for defined scientific activities or projects with appropriate independence.
• Support preparation and review of nonclinical/regulatory documentation and safety assessments.
• Develop knowledge across the Nonclinical Development portfolio and provide cross-programme support.
• Be a subject matter expert for projects to support other functions and address inquiries from Health Authorities.

Connaissances

Biology

Pharmacology

Toxicology

Life Sciences

Regulatory knowledge

Scientific writing

Formation

MSc or PhD in Biology

Outils

Imaging (PET)

Imaging (SPECT)

Imaging (CT/MR)

GLP studies

Description du poste

Job Description Summary

This role is for a Nonclinical Scientist and will support the development of diagnostic imaging agents that will make a real impact on the lives of patients. The role combines scientific contribution to nonclinical projects with broader team support, process improvement and development of effective and consistent ways of working. For this position, reporting to the Global Head of Nonclinical Development, you will bring your scientific experience, biology expertise and ability to work in a cross functional team. You will work on the nonclinical aspects of developing imaging diagnostic agents for the diagnosis, differentiation and therapy monitoring of diseases. The individual will contribute scientifically to defined projects and activities, working with more experienced nonclinical scientists and cross-functional teams, while also helping the Nonclinical Development team operate effectively across its portfolio. A key part of the role will be identifying opportunities to simplify processes, improve organisation and information management, establish standard ways of working, and improve visibility and consistency across nonclinical activities. The position is non-laboratory based and will appeal to you if you enjoy working on multiple projects. You will be a critical part of a team working on a broad portfolio of molecular, contrast or ultrasound imaging products in all stages of development, aiding regulatory submissions and the life cycle management of approved products.

Essential Responsibilities

• Contribute scientific expertise in biology, pharmacology, toxicology or another relevant life-science discipline to nonclinical development programmes.


• Support the effective operation of the Nonclinical Development team across multiple projects and programmes.


• Identify and implement opportunities to simplify and improve team processes and ways of working.


• Contribute to continuous improvement initiatives within Nonclinical Development.


• Provide flexible scientific and operational support across the portfolio according to changing business and project priorities.


• Support design, planning, conduct and interpretation of appropriate in vitro and in vivo nonclinical studies.


• Take responsibility for defined scientific activities or projects, with an appropriate level of independence depending on experience.


• Support preparation and review of scientific and regulatory documentation, including nonclinical reports, regulatory submissions, safety assessments, scientific summaries and publications.


• Develop knowledge across the Nonclinical Development portfolio and provide scientific support across programmes where required.


• Be a subject matter expert for projects to support other functions and address enquires from external parties such as Health Authorities.

Qualifications / Requirements

• An MSc or PhD in Biology, Pharmacology, Toxicology or Life Sciences or another relevant Life Science discipline, or equivalent relevant scientific experience.


• Experience and understanding in the field of cardiology, neurology or oncology, with a focus on the areas relevant to therapeutic or diagnostic drug development


• An understanding of imaging (PET, SPECT, CT, MR or ultrasound) is desired, but not essential


• Previous experience with regulatory submissions, GLP safety/toxicology studies and safety risk assessments is preferred, but not critical


• A high degree of initiative and the ability to work systematically and independently is expected


• Proven ability to write high-quality documentation in English


• Excellent communication skills


• Good collaborative working practices

Company Culture

GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world. GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law. We expect all employees to live and breathe our behaviors: act with humility and build trust; lead with transparency; deliver with focus; and drive ownership – always with unyielding integrity. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration, and support. #LI-MB1 #LI-hybrid

Additional Information

Relocation Assistance Provided: No

At GE HealthCare, we see possibilities through innovation. We’re partnering with our customers to fulfill healthcare’s greatest potential through groundbreaking medical technology, intelligent devices, and care solutions. Better tools enabling better patient care. Together, we are not only building a healthier future but living our purpose to create a world where healthcare has no limits.