Clinical Research Coordinator
Exciting opportunity to have a direct impact on patient care. Australia's leading allograft service provider is looking to add to the R&D team.
Summary about this job
Clinical/Medical Research
Company: Australian Biotechnologies
Location: Sydney
Work type: Full Time
Salary: n\a
Phone: +61-2-3636-9307
Fax: +61-3-6533-8735
E-mail: n\a
Site: n\a
Detail information about job Clinical Research Coordinator. Terms and conditions vacancy
The Company
Australian Biotechnologies manufactures allograft solutions for a wide range of patient needs and surgical procedures. Australian Biotechnologies’ world-class manufacturing facilities and proprietary processing technology have become renowned as the gold standard of allograft production and Australia's leading manufacturer of allograft implants. We are committed to research and development, focusing on ensuring safety whilst improving clinical efficacy.
We are seeking to recruit a full or part time Clinical research Co-ordinator to join our R&D team.
The Role
You will have the opportunity to focus on innovative therapeutic products that will have a direct impact on patient care and community health. You will be responsible for the co-ordination, management and monitoring of clinical and pre-clinical studies.
Some of your key responsibilities will include:
- Coordinate and manage a number of trials concurrently.
- Ensure accurate and timely source documentation and data entry, and the maintenance of essential documents that validate integrity in the conduct of the clinical trials and research.
- Interpretation of clinical data
- Liaise with surgeons, health professionals, principal investigators, multidisciplinary team and Trial Monitors.
- If required present the information to the public and/or health professionals.
To ensure your success in this role you will need to possess the following essential skills, education and experience.
- Substantial understanding of the clinical trial environment and ICH GCP.
- Experience in research and/or coordinating/conducting clinical trials.
- Writing human clinical trial protocols.
- Collation of results and reporting of outcomes in a standardised manner.
- Initiating additional clinical documentation activities as they arise.
- Have excellent interpersonal skills.
- Tertiary qualification or equivalent in clinical research, medical science or pharmaceuticals science.
- Solid administrative and computer skills.
In addition to the above skill set, you will also have a positive attitude and have a commitment to maintaining high ethical standards. We are a company with a great teamwork culture, so we are looking for someone to be part of the team.
Salary will be dependent on experience. Immediate start available.
If you are interested in applying for this position, please submit your resume and cover letter via the ''Apply for this job"" button.
Please note due to the high number of expected applications, only shortlisted candidates will be contacted for an interview.