About the opportunity The key objectives of the Registered Midwife - Clinical Research Coordinator position is to support high quality clinical research and maintain optimum health care to research participants at the standard of practice, in accordance with the National Health Medical and Research Council (NHMRC), Good Clinical Practice (GCP) Guidelines and the International Committee of Harmonisation (ICH).
The incumbent will contribute to the research team lead by a nominated Principal Investigator (PI), and develop research expertise through the pursuit of defined projects relevant to a specific service group within the Townsville Hospital and Health Service (THHS).
The title of the study is: Developing novel tests to detect fetal growth restrictions in regional and remote areas.
PLEASE NOTE - This is a temporary part-time role, up to two (2) years, working 30.4 hours per fortnight (with a possibility of an additional 12 months extension).
About your new employer Supportive Workplace Culture and Regional Advantage A strong community-driven culture makes our organisation an attractive workplace, fostering collaboration, inclusion, and professional support.
We balance metro-level healthcare opportunities with a regional feel, offering short commutes, access to rural and urban facilities and a close-knit professional network.
Employees experience a unique blend of career growth and lifestyle flexibility without the hustle of larger cities.
Work/Life Balance and Lifestyle Benefits Nestled within beautiful North Queensland, the rural, urban, country and coastal locations found within the Townsville HHS region provides vibrant and unique communities, affordable living with stunning landscapes, outdoor adventures, and a relaxed lifestyle.
Competitive salary and benefits: We offer attractive remuneration packages and .
Salary range: $***** - $***** p.h. (NG5) 4 weeks annual leave (pro rata) with 17.5% loading Professional Development leave and allowance Locality and Uniform allowance *****% employer contribution to superannuation Plus options may be available Requirements: Qualifications: Bachelor of Midwifery or equivalent is a mandatory qualification for this position.
Highly Desirable: Research or clinical trial coordination experience Demonstrate clinical skills in IV cannulation.
If not competent in this skill, must be willing to undertake necessary training during the term of this employment.
Possession of a relevant postgraduate qualification in an appropriate field is highly desirable.
Such experience may be discipline specific or have a service area focus.
GCP – Good Clinical Practice certification, or the willingness to acquire within one month of commencement.
This is a VPD risk role.
Hepatitis B, Measles, Mumps, Rubella, Varicella, Pertussis and Tuberculosis.
Please refer to the Role Description for further details.
Apply now and be part of something extraordinary
Enquiries are welcome; please contact: Sonja Brennan on ************** Applications close: Wednesday, 17 December **** Unsolicited resumes from recruitment agencies will not be accepted.
Please download the Role Description from the `Documents' section below for application/interview preparation and future reference.