Senior Clinical Research Associate / Clinical Research Associate
IQVIA is looking for a SCRA/CRA to join it's Core and Customer dedicated teams. Offering global exposure, career development and opportunity.
Summary about this job
Clinical/Medical Research
Company: IQVIA
Location: Melbourne
Work type: Full Time
Salary: n\a
Phone: +61-3-9351-8098
Fax: +61-7-7495-5858
E-mail: n\a
Site: n\a
Detail information about job Senior Clinical Research Associate / Clinical Research Associate. Terms and conditions vacancy
- Global CRO giving you experience to new and developing clinical departments
- Career develoment arcoss both the Commercial and R&D sides of IQVIA
- Competitive salary package including employee focused benefits
IQVIA is currently looking for experienced Senior Clinical Research Associate (SCRA) or Clinical Research Associate (CRA) to join it Core and Customer Dedicated teams. These positions are full-time and ongoing.
As you develop your career as a CRA, these roles offer you the opportunity to plan and progress your career in the direction you choose. At IQVIA, we do not believe in a 'career ceiling.' You can make the Senior/CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won't do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.
Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You will be building a smart and flexible career with no limits.
While projects vary, your typical responsibilities might include:
- Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
- Supporting the development of a subject recruitment plan
- Establishing regular lines of communication plus administering protocol and related study training to assigned sites
- Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
- You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.
You should have:
- A Bachelor's degree in a health care or other scientific discipline or educational equivalent
- At least 2 years of local on-site monitoring experience, ideally including monitoring clinical trials in Australia or New Zealand
- Experience monitoring Oncology clinical trials will be highly regarded.
If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team.