Clinical Trial Assistants contribute significantly to the success of clinical projects.
This role requires strong administrative support to ensure timely completion of project objectives. With a flexible working arrangement that balances work and life, this position is ideal for individuals seeking a dynamic work environment.
Key Tasks:
* Coordinate Clinical Trial Supplies, ensuring accurate tracking information.
* Maintain clinical documents and systems, such as eTMF and CTMS, to ensure site compliance and performance.
* Provide expert support for clinical team communications, correspondence, and associated documentation.
* Support clinical monitoring duties on site visits, following required training and approval.
Essential Qualifications:
* Minimum 6-12 months experience in a related role.
* Ability to accurately update and maintain clinical documents and systems.
* Superb communication, computer, and problem-solving skills.
* Familiarity with clinical research regulatory requirements, including GCP and ICH guidelines.
* High school diploma or equivalent, plus 3 years of administrative support experience, or equivalent combination of education and experience.
Our Benefits:
* Professional growth and development opportunities.
* Comprehensive leave policies and health allowance.
* A supportive work environment that prioritizes work-life balance.
* A collaborative team atmosphere with experienced leaders.
* An inclusive company culture with parental leave benefits.