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 **
Our Medical Affairs Scientists are knowledgeable individuals who are passionate about ensuring that OGT’s products are safe, effective, and fit for purpose, thus allowing them to be available globally and state of the art. You will play an integral role in the delivery of internal and external analytical and clinical performance data for a range of OGT products.
What you’ll be doing for us:
To work as part of a team in executing tasks as directed, but not limited to, the following activities:
Contribute to the documentation and infrastructure of the department by overseeing the writing of internal and external protocols, study plans and reports
Participate in the design, implementation and delivery of any required studies
Identify and engage external laboratories, clinicians, and partners to obtain clinical performance data
Support and coordinate external studies, including collaboration, data sharing, and contracting activities
Collaborate with internal and external stakeholders to support project delivery
Manage and coordinate projects activities from initiation through to completion
Analyse and interpret data across diagnostic techniques and deliver scientific, clinical, and analytical reports in a timely manner
Ensure timely and accurate reporting of study results
Provide clinical/scientific input for product brochures, catalogues and other marketing materials when required
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
Support validation activities for team equipment and software, and support maintenance of risk management documentation in line with ISO 14971
Provide training and support to medical affairs analysts and assistants as appropriate
Provision of analytical teaching within and outside of the medical affairs team as appropriate
Analysis of FFPE and haematological specimens using manual microscopes and automated software
Support karyotype analysis of G banding and reverse DAPI FISH images
To complete any other tasks as commensurate with the level and nature of the post as delegated by the line manager.
What we are looking for in you
Essential
A bachelor’s degree in molecular biology, biochemistry, genetics, biotechnology, or similar subject is required
Knowledge of FISH and/or cytogenetics techniques and their clinical applications
Understanding of clinical diagnostics, laboratory workflows, or molecular testing
Ability to engage confidently with external partners, including laboratories, clinicians, and collaborators
Proven ability to proactively drive activities forward
Experience drafting study protocols or similar technical/scientific documentation
Understanding of study design considerations, including objectives, endpoints and data requirements
Strong organisational and project coordination skills, managing activities from initiation through to completion
Ability to interpret clinical or diagnostic data, including comparison across different testing methodologies
Experience handling sensitive or clinical data, with an understanding of data quality and governance requirements
Excellent communication skills, both written and verbal.
Desirable
Cytogenetics experience in an NHS laboratory or equivalent
Experience in data acquisition, clinical studies, or external collaborations
Experience setting up or supporting contracts, agreements, or study arrangements with external partners
Familiarity with disease areas, sample types, and appropriate testing approaches
Awareness of commercial or customer-facing environments, particularly in diagnostics or life sciences
Experience supporting clinical performance evaluations, validation, or regulatory activities
Experience in cytogenetics and or Karyotype analysis.
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.