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Full-time, Temporary
bachelor degree
Pension Scheme, Private Health Insurance, Private Dental Insurance, Group Income Protection, Group Life Assurance, 25 days holiday
Posted 4h ago
~40 hrs/week
Responsibilities
The Medical Affairs Analyst will perform hands-on laboratory tasks, including sample analysis and microscopy, while managing technical documentation and quality control. They will also collaborate with internal teams to support clinical projects, regulatory compliance, and the maintenance of the Quality Management System.
Requirements
Candidates must have a background in a science-related subject and experience working in a GLP environment. Strong understanding of biosafety, regulatory requirements, and proficiency in data handling are essential for this role.
Full job description
OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personalised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines.
This position is a fixed-term contract, ending in December 2028
An opportunity has arisen in our Medical Affairs team for a Medical Affairs Analyst. This role offers a varied mix of hands‑on laboratory work and administrative responsibilities, supporting Cytocell FISH probe technical files.
What you’ll be doing for us:
Core
Work with clinical and/or biological data and materials, ensuring accurate handling, tracking, and documentation
Responsible for an assigned proportion of clinical/analytical project work
Collaborate with internal teams & external labs or companies to support project specific sample requests in line with internal procedures and external regulations
Contribute to the Quality Management System and infrastructure of the department by providing input into internal protocols and implementation of CAPAs, change controls and improvements
Accurately follow SOPs and defined processes
Maintain high levels of accuracy and attention to detail in all tasks and outputs
Conduct data validation and/or quality checks prior to reporting any data
Support high-volume report generation within defined timelines
Contribute to audits and implement corrective actions and improvements
Review marketing materials for scientific and clinical accuracy
To complete any other tasks as commensurate with the level and nature of the post as delegated by the line manager.
As Required
Responsible for the timely procurement of samples
Analysis of haematological and FFPE specimens using manual microscopes and automated software
Cover additional laboratory duties including biological sample culturing and harvesting (e.g., peripheral blood samples), image capture, receipt and logging of external samples, maintenance and use of internal samples and accurate upkeep of laboratory records
Karyotyping/chromosome identification using reverse DAPI analysis or G-banding
Responsible for setting up HTA projects in collaboration with project owner
Run and monitor automated reporting workflows (e.g. R-based pipelines)
Identify and resolve issues in the report generation (e.g. input data or processing errors), escalating more complex problems as needed
Contribute to risk management activities, including maintaining documentation in line with ISO 14971
Support periodic risk reviews and updates as part of product lifecycle management
Conduct literature reviews to support clinical evidence
Contribute to development of Scientific Validity reports and other clinical evidence documentation
Support preparation and review of clinical and regulatory documentation
Provide support in the validation of equipment and software as appropriate for the team.
What we are looking for in you
Essential
Background in a science related subject
Experience of working in a GLP environment
Knowledge of the human tissue act
Previous experience of working with samples
Strong understanding of biosafety, chain of custody, and regulatory requirements
Strong computer literacy, including confidence using tools such as Excel for data handling and organisation
High level of attention to detail, with the ability to check data and outputs for accuracy and consistency
Good organisational and time management skills, with the ability to manage multiple tasks and meet deadlines
Comfortable working with data, including maintaining accurate records and handling information appropriately
Ability to work independently on routine tasks, while knowing when to seek support
Able to work accurately and efficiently in a high-volume, process-driven, and protocol-driven environment
Good document practice
Excellent communication skills, both verbally and written
Ability to train others.
Desirable
Knowledge of FISH and or other cytogenetics techniques
Exposure to R or other data analysis tools (e.g. running scripts, basic troubleshooting)
Ability to identify and resolve issues in data or automated reporting workflows, with support where needed
Awareness of data validation or quality control processes
Experience or awareness of clinical diagnostics or laboratory environments
Experience supporting data collection, analysis & reporting
Exposure to project coordination or workflow tracking
Exposure to clinical evidence generation, literature review, or scientific writing
Awareness of risk management processes or standards (e.g. ISO 14971)
Experience supporting clinical or regulatory documentation
Experience in equipment/software validation.
In return you will receive:
Competitive salary
Pension Scheme (10% non-contributory)
Private Health Insurance
Private Dental Insurance
Group Income Protection
Group Life Assurance
25 days holiday plus UK bank holidays
High Street Discount Scheme.
Application is via CV and a one-page covering letter outlining your suitability for the role, salary expectations and notice period.
Please note that we will need to establish your right to work during the recruitment process.
Related keywords
Medical AffairsGenomicsCytocellFISHGLPHuman Tissue ActBiosafetyCAPAISO 14971KaryotypingDAPIG-bandingR-based pipelinesClinical diagnosticsRegulatory documentationQuality control
As a leading global provider of diagnostic genomic solutions, our goal is to enable researchers and clinical decision makers to reach the right decisions for each patient, every time.
The quality and innovation built into our products for NGS, arrays and FISH reflects our commitment to improving the future of genetic clinical care.
We offer partnership and collaboration to our customers at every stage of their work.
Offices: Unit 5, Oxford Technology Park, 4A Technology Drive, Kidlington, Oxfordshire OX5 1GN, GB · 418 Cambridge Science Park, Milton Road, Cambridge, Cambridgeshire CB4 0PZ, GB · 520 White Plains Road, Suite 500, Tarrytown, New York 10591, US
Microarray productsFluorescence in situ hybridisationSequencing productsFISH probesNGS productsand next generation sequencingGenetics
How many Science & Research jobs are open in Cambridge, United Kingdom right now?
There are currently 315 open science & research positions in Cambridge, United Kingdom listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Science & Research roles in Cambridge, United Kingdom?
Companies currently hiring include Riverlane, Awerian Ltd, Danaher, Graphcore, AstraZeneca, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Science & Research jobs in Cambridge, United Kingdom?
Yes — 152 of the 315 open science & research positions offer remote or hybrid work (20 remote, 132 hybrid).
How do I apply for Science & Research jobs in Cambridge, United Kingdom?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.