Global Clinical Trials Specialist
Are you ready to take your career to the next level? As a leading global contract research organization, we are seeking a highly skilled Global Clinical Trials Specialist to join our team.
We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development solutions across multiple therapeutic areas.
* Our specialists enjoy working on cutting-edge global clinical trials, have experienced and supportive managers, career development pathways, and opportunities to work with dedicated sponsors.
Your Key Responsibilities:
* Conduct site monitoring visits, including routine monitoring and closeout of clinical sites, maintenance of study files, and conduct of pre-study and initiation visits.
* Liaise with vendors and ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools.
* Ensure audit readiness at the site level, prepare accurate and timely trip reports, and participate in Quality Control Visits (QC).
To be successful as a Global Clinical Trials Specialist, you will require:
* A university or college degree, or certification in a related allied health profession from an accredited institution.
* Demonstrated experience of at least 18 months in onsite monitoring global clinical trials from SIV to Close-out.
* Understanding of local regulatory guidelines and willingness to travel interstate for site monitoring visits.
Benefits of Working with Us:
* We offer competitive compensation packages and opportunities for professional growth and development.
* Our team members enjoy a dynamic and supportive work environment, with regular feedback and coaching to help them achieve their goals.