FAQs
What is the primary role of a Genomic Associate in the Cancer Genetics team?
The primary role of a Genomic Associate is to facilitate the genomic investigation journey by collaborating with patients, relatives, clinical services, and genomic laboratories to improve access to care and ensure timely and high-quality services for patients.
Where will the Genomic Associate be based?
The Genomic Associate will be based in the Clinical Genetics Service at Northwick Park Hospital.
What are the responsibilities of a Genomic Associate?
Responsibilities include contacting patients to verify referral information, obtaining genetic test reports, gathering family history information, arranging screenings for high-risk individuals, and liaising with laboratories and clinical teams to track and facilitate the collection of relevant tissue/samples and testing.
Is there an opportunity for professional support in this role?
Yes, the Genomic Associate will work alongside clinical geneticists, genetic counsellors, and other healthcare professionals, providing ample opportunity for professional support and collaboration.
What specific data tasks will the Genomic Associate perform?
The Genomic Associate will enter data for online cancer risk assessments, generate risk calculations using tools such as CanRisk, and keep spreadsheets and records updated.
Will the Genomic Associate contact healthcare professionals?
Yes, they will contact healthcare professionals to ensure all appropriate information is received before clinic appointments and to discuss referrals.
What kind of training or supervision will the Genomic Associate receive?
The Genomic Associate will work under supervision, which includes training on protocols and procedures relevant to genetic testing and patient interaction.
How does this role contribute to patient care?
The role contributes to patient care by ensuring that patients and their families receive timely genetic testing, accurate information, and support throughout the genetic investigation process.