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Nonclinical Scientist
GE HealthCare. Contribute scientific expertise in biology, pharmacology, toxicology or another relevant life-science discipline to nonclinical development programmes .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Biology, Pharmacology, or Toxicology with a focus on nonclinical development, regulatory submissions, and safety assessments. Proven ability to support scientific documentation and collaborate effectively across multidisciplinary teams.
Highest-signal resume keywords
MSc Or PhD In BiologyPharmacology ExpertiseToxicology KnowledgeRegulatory Submissions ExperienceIn Vitro And In Vivo Study Support
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Scientific Documentation WritingSafety Risk AssessmentsGLP Safety StudiesTherapeutic Drug DevelopmentDiagnostic Drug Development
Soft Skills
Excellent Communication SkillsHigh Degree Of InitiativeCollaborative Working Practices
Tools & Technologies
Imaging TechniquesPETSPECTCTMRUltrasound
Industry Keywords
Nonclinical DevelopmentLife SciencesCardiologyNeurologyOncology
About the role
Key responsibilities & impact- Contribute scientific expertise in biology, pharmacology, toxicology or another relevant life-science discipline to nonclinical development programmes
- Support 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
- 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
- Act as a subject matter expert for projects, support other functions and address enquiries from external parties such as Health Authorities
Requirements
What you’ll need- 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 cardiology, neurology or oncology, focused on therapeutic or diagnostic drug development
- Understanding of imaging (PET, SPECT, CT, MR or ultrasound) desired but not essential
- Previous experience with regulatory submissions, GLP safety/toxicology studies and safety risk assessments preferred but not critical
- High degree of initiative and ability to work systematically and independently
- Proven ability to write high-quality documentation in English
- Excellent communication skills
- Good collaborative working practices
Benefits
Comp & perks- Salary and benefits package
- Career opportunities
- Culture fostering care, collaboration, and support
- Relocation assistance not provided