The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Tobacco Research Group (TRG) team. The CRC will coordinate the successful management of research activities for a Smoking Cessation Trial. You must have previous experience in coordinating a clinical trial and be able to travel occasionally within Greater Sydney.
Responsibilities include:
- Assist in developing and maintaining the relevant study materials (clinical protocol, standard operating procedures, Investigator’s Brochure, data collection tools, case report form, participant information and consent forms, study documentation, etc) in accordance with TGA, ICH Good Clinical Practice and CONSORT guidelines.
- Ensure adverse events are properly documented and reported to the Sponsor and Ethics Committee as appropriate.
- Coordinating project/ investigator meetings, advisory committee meetings and oversee the smooth running of the clinical trial and ensure adherence to trial protocol management.
- Conduct and assist with systematic review(s), literature searching, data collection, analysis and paper write-up/drafting.
- Contribute to the development of successful recruitment strategies for the trials, including developing effective working relationships with appropriate stakeholders.
- Coordinate the development and maintenance of study documents to ensure milestones are met and outcomes achieved.
- Maintain a high level of professional expertise through familiarity with research literature.
