Registrar - Unaccredited - Anaesthetic Research

Company description:

Peter MacCallum Cancer Centre

Job description:

Position Summary

The Department of Anaesthetics, Perioperative Medicine and Pain Medicine requires a Research Assistant to help with the conduct of Clinical Trials within the department. Applicants are invited to join an exciting research team focused on pharmacogenomics in the perioperative period. The research assistant will coordinate and deliver direct and indirect care and associated data collection for pharmacogenomic trials and assist with other research studies undertaken in the department. The research assistant will practice in accordance with the Therapeutic Goods Administration (TGA) Note for Guidance on Good Clinical Practice (CPMP/ICH/135/95) and the National Health and Medical Research Council (NHMRC) National Statement on Ethical Conduct in Research Involving Humans. This role requires meticulous adherence to trial protocols, a commitment to safe work practices, and significant organisational and project management skills. The successful candidate will be capable of working in an independent manner within an existing team.

Enterprise Agreement

Doctors in Training Enterprise Agreement

Classification or Salary Range

As per experience based on award

Immunisation Risk Category

Category A

Key Relationships

Internal:

• Research study patients
• Anaesthetic staff within the Department of Anaesthetics, Perioperative Medicine and Pain Medicine
• Surgical staff
• Clinical nurses in all relevant patient care areas - including theatres, OPD and wards.
• Multidisciplinary team members
• Clinical Trial Co-ordinators
• Clinical Trial Principal Investigators
• Departmental research team
• Laboratory staff
• Health information services department
• Internal human research ethics committee (HREC)
• Clinical Research Development and Operations (CRDO) office

External:

• Clinical Trial Co-ordinators
• External laboratories and diagnostic imaging centres

Skills Certifications, Licenses & Registrations AHPRA Registration Key Accountabilities Demonstrated by / Key Performance Indicators

1. To effectively follow clinical research protocols

• Follow clinical trial protocols and conduct clinical research trials is in accordance with TGA ICH GCP and the NHMRC National Statement on Ethical Conduct in Research Involving Humans
• Willingness to learn.
• Thorough and accurate note- and record-keeping.
• Able to make appropriate clinical and professional autonomous decisions as required & seek clarification where necessary.
• Maintain a flexible approach to working hours in order to meet the requirements of research protocols and subject recruitment (including evening and weekends as required).

• Liaise with all involved groups/departments to ensure all biological samples are collected, processed, stored as per protocol.

• Responsibility for Biospecimen collection, processing and banking.

• Proficiency in biospecimen processing and research sample preparation.

• Co-ordination of biospecimen labelling, banking and shipping.
• Accurate and timely entry of data.
• Timely upkeep of stocks and consumables.

• Maintaining a clean and organised work environment.

• Compliance with Anaesthetics Perioperative Medicine and Pain Medicine Research expectations, and commitment to values

• Up-to-date records of all mandatory and job-specific training courses.

• Prompt disclosure of any conflict of interest for all commercial or project-based research.
• Maintenance of commercial confidence, protection of sensitive information and compliance with any non-disclosure conditions.
• Mandatory reporting of safety incidents, near-misses and identified risks.
• Commitment to inclusive, diverse and respectful workplace culture.