Research Scientist

Found in: Jooble UK C2 - 2 weeks ago

Surrey, United Kingdom Thyme Full time

Datar Cancer Genetics Job Title: Clinical Scientist (HCPC registered)
Location: Hybrid (2-3 days on site)
At Datar, we are a leading molecular genetics and cell culture laboratory committed to delivering innovative solutions to improve patient outcomes. This is an exciting opportunity to contribute to cutting-edge technology and make a meaningful impact on healthcare advancements.

As a Clinical Scientist, you will play a crucial role in Data analysis, Results reporting, Collaboration and Communication, and Quality Assurance. The successful candidate will collaborate with interdisciplinary teams and external stakeholders, support business development activity with technical know-how, and ensure compliance with regulatory standards. This role requires a strong scientific background, excellent analytical skills, and a passion for advancing medical knowledge.

Data Analysis, Interpretation and Reporting:
Conduct analyses of lab data to generate reports and support evidence-based decision-making for prescribing medical practitioners.
Regulatory Compliance:
Ensure all Laboratory activities adhere to relevant regulatory standards and guidelines.
Prepare and submit documents to obtain accreditations and regulatory approvals for the company’s services.
Collaborate with internal and external stakeholders, including investigators, clinicians, and regulatory authorities.
Communicate effectively with team members to ensure the successful implementation of the laboratory processes.
Understand the past and ongoing research conducted by the company and other similar studies elsewhere, and be able to explain the comparative evidence base to the healthcare professionals.
Understand the reports produced in the diagnostic lab and be able to explain the expected format to the prescribing medical practitioners.
Quality Assurance:
Implement and maintain quality assurance processes to ensure the integrity and accuracy of laboratory processes.
Assist in the implementation of ISO 15189 quality standards and practices.
Post-graduate or equivalent in a relevant scientific discipline (e.g., Medicine, Biology, Pharmacology).
Proven experience in data analysis and reporting.
Strong understanding of statistical methods and data analysis.
Familiarity with relevant regulatory requirements in the UK.

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