Senior Clinical Research Associate or Clinical Research Associate
You will be responsible for performing activities associated with the evaluation, initiation, monitoring and close out of clinical trials.
Summary about this job
Clinical/Medical Research
Company: CPR Pharma Services Pty Ltd
Location: Adelaide
Work type: Full Time
Salary: n\a
Phone: +61-3-1947-6255
Fax: +61-3-6961-7063
E-mail: n\a
Site: n\a
Detail information about job Senior Clinical Research Associate or Clinical Research Associate. Terms and conditions vacancy
CPR Pharma Services ('CPR') is a full-service CRO offers which offers specialised services supporting drug development for the pharmaceutical and biotechnology industry with an international reputation for delivering superior clinical trial results in Asia-Pacific region. We are the premier provider of early phase clinical trial services in the region for over a decade.
Opportunity
An opportunity has arisen for a highly motivated, adaptable and experienced Senior Clinical Research Associate (SCRA) or Clinical Research Associate (CRA) to join the Clinical Services Team at CPR. Reporting to the Clinical Operations Manager, this is an office based full-time permanent position.
We offer training opportunities, flexibility and work-life balance, opportunities for growth and development and all within a fun and stable culture.
The Role
Acting as the primary link between sites and sponsor, you'll be responsible for:
- Performing start-up, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice
- Coordinate the required activities of stakeholders in the clinical project management process including sponsor, site and monitors
- Developing your skills and knowledge on clinical trials within a wide scope of therapeutic areas
- Monitoring all aspects of studies to ensure compliance with GCP, study protocol and regulatory requirements and prepare monitoring reports
- Development and review study protocols and other study related documents
- Preparing ethics submissions and assist in preparation of Clinical Study Reports
To be successful in this role, we are looking for candidates with:
Prior experience monitoring clinical trials, ideally within Australia and/or New Zealand. It is essential that you have a degree in science or other healthcare related discipline, at least 3 - 5 years experience working as a S/CRA and 3-5 years experience in the pharmaceutical industry / CRO. Good knowledge of Australian and New Zealand drug development process, clinical trial monitoring procedures, GCP guidelines and medical terminology is essential. On top of this you will need to able to show initiative and work well autonomously, within minimal supervision. You will be an excellent communicator who is passionate about clinical research and who is quality and customer focused.
To apply
Please click on the 'apply for this job' link and submit your CV along with a cover letter outlining your skills and experience that make you suitable for this role, please submit as one Microsoft Word document.
To be considered for this role you must be able to provide evidence of entitlement to work in Australia.
As we receive a high volume of applications for our vacancies, we will only contact you directly, should you be successful through to the next stage of our recruitment process.
For further information about CPR Pharma Services, please visit our website at http://www.cprservices.com.au
CPR Pharma Services is an equal opportunity employer