Cranmore Executive Search | Cranmore Life Science
Senior Scientist
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Senior Scientist
Reports To: Lead Scientist/R&D Manager Employment Type: Permanent, Full-time
About the Role
The Senior Scientist provides technical leadership within R&D projects, contributing to strategic experimental design and execution. The role involves independently leading defined workstreams, mentoring junior staff, and ensuring high-quality scientific output aligned with program objectives.
About the Company
Our client is an innovative biotechnology company developing advanced drug delivery technologies, combining cutting-edge biomaterials science with pharmaceutical development to improve treatment outcomes and patient experience.
Position Summary
The Senior Scientist is tasked with driving technical progress while ensuring scientific rigor and strategic alignment. The role requires both hands-on leadership in project execution and guidance for junior organisational members.
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Essential Duties and Responsibilities
- Lead experimental design and execution for defined project workstreams
- Provide scientific oversight, ensuring data quality and integrity
- Interpret complex datasets and offer strategic recommendations
- Mentor Laboratory Technicians and Scientists
- Contribute to project planning, timelines, and risk mitigation
- Author and review technical reports, presentations, and publications
- Drive continuous improvement in laboratory and analytical processes
- Ensure compliance with ISO9001 and regulatory standards
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Required Qualifications
- PhD in a relevant scientific discipline (evidence of industry experience required)
- Demonstrated experience leading R&D workstreams or technical projects
- Advanced expertise in analytical techniques and pharmaceutical formulation
- Strong project management and organisational skills
- Excellent communication and cross-functional collaboration abilities
Preferred Qualifications
- Experience in biologics, polymer development, or advanced drug delivery systems
- Experience operating in ISO9001, ISO13485, and/or cGMP environments
- Familiarity with regulatory documentation processes
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