Description:
How refreshing it is to hear of an organisation that will prioritise working on the best studies, with the best sponsors first?
How does it make you feel that an organisation wants to mentor and prepare you for developing within a business that is experiencing exponential growth?
This leading Clinical Research Site based in the Sydney City Fringe is conducting innovative and impactful clinical trials to improve patient outcomes. The collaborative environment offers the perfect setting for professionals passionate about making a difference in healthcare.
We are seeking an experienced and motivated Clinical Trials Site Study Coordinators to oversee the day-to-day management of these clinical trials. You will play a crucial role in ensuring the smooth operation of the studies, maintaining compliance with regulatory requirements, and providing exceptional care to study participants.
- Coordinate and manage clinical trial activities from initiation to completion.
- Obtain informed consent from study participants and ensure their rights and well-being are protected.
- Schedule and conduct study visits, including the collection and documentation of data.
- Maintain accurate and up-to-date study records and databases.
- Communicate effectively with study investigators, sponsors, and regulatory bodies.
- Ensure compliance with Good Clinical Practice (GCP), ethical standards, and regulatory guidelines.
- Assist in the preparation of study protocols, reports, and other documentation. Provide training and support to study staff and participants as needed.
Required
- Bachelor's degree in a related field (e.g., Nursing, Life Sciences, or equivalent)
- Must have a nursing background prior to working in Clinical Trials
- Must have Early Phase Oncology experience
- Minimum of 2 years of experience in clinical trials coordination or a similar role
- Strong understanding of clinical trial processes
- Effective communication and interpersonal skills
- Ability to work independently and as part of a team
- Proficiency in using CTMS and EDC systems
On offer
- Competitive salary and benefits package
- Opportunities for professional development and career advancement
- A supportive and collaborative work environment
- The chance to contribute to cutting-edge clinical research and improve patient outcomes.
How to Apply:
If you are passionate about clinical research and meet the qualifications listed above, we would love to hear from you. Press apply or contact Dana Sarkissian on
02 8310 5842
dsarkissian@i-pharmconsulting.com