Clinical Research Associate
This CRA will work in an international CRO, dedicated to one pharmaceutical sponsor in Melbourne.
Summary about this job
Clinical/Medical Research
Company: Hays Life Sciences
Location: Melbourne
Work type: Full Time
Salary: n\a
Phone: +61-2-9509-7342
Fax: +61-3-8145-4751
E-mail: n\a
Site: n\a
Detail information about job Clinical Research Associate. Terms and conditions vacancy
- Excellent in- house support, systems and processes
- Clear career opportunities
- Possibility to work with the sponsor directly
This CRA will work in an international CRO, dedicated to one pharmaceutical sponsor in Melbourne.
Your new company
An exciting opportunity to working in a highly rewarding role for a local CRO out-sourced to a single Pharmaceutical sponsor. This CRO is committed to supporting your career development working at the highest standards of ethics and integrity. They are renowned for their social organisational culture and boast a high staff retention.
Your new role
Working on a permanent basis as a CRA, you will be representing the CRO and will perform routine monitoring visits. Working to a single set of SOP's, you will take on all study monitoring activities, from pre-study through to close-out. Your responsibilities will include:
- Ensure adherence to the project plans / protocols/ regulatory and GCP obligations
- Participate in investigator meetings
- Ensure the integrity of all data submitted
- Contribute to identify potential investigators
- Provide update and trial status reports
- Manage travel expenses economically
- Liaise with site staff and continually communicate with
- Principal investigators, client company and project team
You will need to be self-motivated, eager to learn and passionate about clinical research. Working independently with the sponsor, you will present yourself well and have strong attention to detail. You will have 2 years of independent monitoring experience across a range of Phases and Therapeutic areas and a Bachelor's level degree in life sciences or similar discipline.
Responsible to maintaining site relationships, you will have excellent communication skills and will support the site staff with protocol adherence. You will have a thorough understand of ICH GCP guidelines and confidently resolve issues as they arise.
You will have a strong desire to travel around 50% of the time and be keen to develop and maintain long standing site relationships.
What you'll get in return
You will be working in a continuously growing, leading organisation with a number of development opportunities and a strong client base.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or send a copy of your CV to Krisztina Auth at [email protected]
If this job isn't quite right for you but you are looking for a new position in clinical research, please contact us for a confidential discussion on your career needs.
If you know somebody who would be interested in this role, we offer a $250 reward scheme for referrals upon successful placement.