Clinical Research Associate
PSI is expanding it's presence in Australia and looking to recruit a Clinical Research Associate to work collaboratively with our Project Team.
Summary about this job
Clinical/Medical Research
Company: PSI CRO Australia Pty Ltd
Location: Sydney
Work type: Full Time
Salary: n\a
Phone: +61-7-7747-6511
Fax: +61-3-8650-8086
E-mail: n\a
Site: n\a
Detail information about job Clinical Research Associate. Terms and conditions vacancy
About Us:
PSI is the Contract Research Organisation that cares – for our staff, our clients and our partners.
A dynamic, global company founded in 1995, we bring together more than 1,600 driven, dedicated and passionate individuals from across 55 countries. We focus on delivering quality and on-time services across a variety of therapeutic indications.
The Role:
As a Clinical Research Associate you will work at the frontline of projects, ensuring timelines, targets and standards on clinical research projects in a variety of therapeutic indications.
Whilst building and maintaining relationships with clinical sites and investigators, with a key focus on monitoring tasks including safety, quality and data compliance.
Responsibilities:
- Prepare, conduct and report on selection, initiation, routine and closeout monitoring visits
- Site management of clinical research studies in Australia and/or New Zealand
- Monitoring trial progress and ensuring project timelines are met
- Facilitation of site budgets and contract negotiations
- Delivering onsite training of investigators and site staff
- Preparation for and attend company's audits and resolution of audit findings
- Maintenance of appropriate documentation regarding clinical site management
- Participation in feasibility research and query resolution
- Contact for clinical investigators, vendors and support services in regard to study progress
The Opportunity:
- Flexibility to work from home
- Work on a global level with global exposure
- 5 weeks annual leave
Skills and Experience:
- University degree in Life Sciences, Pharmacy, MD or RN or an equivalent combination of education, training and experience
- 2 – 3 years of independent monitoring experience in Australia, with full scope of monitoring responsibilities within Phase II/III Clinical Trials
- Experience in regulatory submissions, contract negotiations, site management and feasibility assessments
- Experience in Multiple Sclerosis, Oncology and Hematology studies
- Fluent English, spoken and written
- Valid driver's license and the ability to travel
- Full working rights in Australia
How to Apply:
Send your CV using the ‘Apply’ link.
Only shortlisted applicants will be contacted.
No agencies please.