Grade 1 Medical Scientist - nexomics

Position Summary

 To provide molecular testing in molecular haematology by use of various techniques including real-time PCR, HRM, fragment analysis and DNA sequencing including next generation sequencing.

This role would suit a candidate that enjoys working in a dynamic environment, can effectively communicate with their co-workers to ensure that all testing is completed within appropriate time frames and has the ability to manage and prioritise multiple tasks.  We provide testing for a number of global clinical trials so strong written and verbal communication skills are essential when liaising with our sponsors.

This role will contribute to the University of Melbourne's partnership with international genomics company Illumina by collaborating with The Advanced Genomics Collaboration by jointly fostering the development of world-leading genomics research and innovation activities and to accelerate the translation of these innovation through to adoption in the healthcare system

Enterprise Agreement

MEDICAL SCIENTISTS, PHARMACISTS AND PSYCHOLOGISTS VICTORIAN PUBLIC SECTOR (SINGLE INTEREST EMPLOYERS) ENTERPRISE AGREEMENT 2021-2025

Classification or Salary Range

Grade 1 (RX1 – RX7)

Immunisation Risk Category

Category A: Position involving direct patient contact, potential exposure to blood, body fluid, human tissue specimens during the course of a normal working day

Key Relationships

Internal 
Senior Clinical Trial Scientists (nexomics)
Clinical trial staff (nexomics)
Anatomical Pathologists
Quality nominees
Pathology staff within Molecular, AP, CSR, Admin, Haematology, Core lab etc.
Clinical Trial Coordinator/Administrator
Business Development team

External
External clinicians and clients
Sponsors, CROs and suppliers

Education

Skills

Essential requirements   
BSc or equivalent in a relevant area of Genetics or Molecular Biology 
Experience as a Medical Scientist in an accredited Diagnostic Molecular Pathology/Genetics laboratory 
Experience with at least two of PCR, real-time PCR, fragment analysis, HRM and automated DNA sequencing, including next generation sequencing. 
Experience in a research laboratory or diagnostic and/or clinical trial testing.
Demonstrable abilities to work effectively within a team.
Works well under pressure and enjoys diverse portfolio of duties as required by the clinical trial portfolio.
Demonstrable abilities to multitask and effectively improve processes.
Attention to detail.
Ability to communicate effectively and promptly utilising electronic and other means.
Proven ability to work cooperatively with pathologists, clinicians, other senior scientists and researchers

Desirable requirements
Experience in clinical data interpretation for real time PCR, HRM analysis and automated DNA sequencing 
Knowledge of automation as applied to nucleic acid based testing including PCR and sequencing. 
Knowledge of emerging technologies for genome based analysis in both germline and somatic situations 

Certifications, Licenses & Registrations

Key Accountabilities

1.Testing for mutations in molecular haematology samples

Providing molecular testing in the area of molecular haematology by use of various techniques including real time PCR, HRM, fragment analysis and DNA sequencing, Perform DNA and RNA extraction as required
Smooth and efficient operation of daily workflow, including specimen receipt, tracking, test performance and reporting as required for the laboratory
Demonstrates an understanding of customer service for internal and external customers and is committed to effectively meeting their needs in a helpful and professional manner.
and adheres to key performance indicators 
Ensures all documentation is completed including procedures, maintenance records and quality assurance procedures according to laboratory, NATA ISO15189 standards and protocols

2.Maintenance and operation of equipment
All equipment is operated and maintained in accordance with laboratory manuals and procedures
Ensures the maintenance records of laboratory equipment are kept according to laboratory protocols.

3.Performs general laboratory duties    
General laboratory duties (eg reagent preparation, waste disposal, laboratory tidiness) performed as required and on request from senior scientists 
Administrative duties as required and on request from senior scientists

4.Work practices are in accordance the laboratory quality systems and procedures
Ensures that work practices are in accordance the laboratory quality systems and procedures at all times 
Ensures that laboratory documentation is up to date at times
Works cooperatively with the Quality Manager
Is familiar with the internal and external quality control activities within the laboratory and complies with the relevant QC protocols
Liaises well with other staff members to ensure that all molecular pathology testing adheres to the relevant protocols

Key Accountabilities (Contd..)

5.Recognizes and reports any clinicallysignificant results to the appropriate staff member and any laboratory problems to senior scientific staff
Seeks the advice of the senior scientific staff to solve a scientific and technical problems in the laboratory
6.Quality Assurance
Participates where appropriate in internal and external QA programs
Promptly reports procedural breakdowns, errors and incidents by means of the non-conformance reporting system
Participates in educational activities including attendance at internal and external training courses, clinical and scientific meetings
Maintains and develops own specialised skills
Embraces skill extension, innovation and change
Participate in any audits, site qualification visits and monitoring visits as required

7.Helps maintain external client base        
Communication with clinical staff and external clients as appropriate 
Cooperates with and assists external clients

8.Works as part of a team        
Communicates and cooperates with co-workers to ensure work is completed within appropriate timeframes

9.Conduct is ethical
Acts in accordance with Institute ethical guidelines and those established by relevant bodies eg NHMRC
Patient confidentiality and privacy is protected
10.Occupation Health and Safety
Adheres to the maintenance of safe working practices and the provision of a safe working environment (as outlined in the OHS legislative and regulations)

11.Follows appropriate policies and procedures
Adheres to the maintenance of safe working practices and the provision of a safe working environment (as outlined in the OHS legislative and regulations)
Acts in accordance with Peter Mac Policies
Acts in accordance with the Australian Institute of Medical Scientists(AIMS) professional code of conduct
Undergoes performance appraisals in accordance with Peter Mac guidelines