As a Clinical Research Associate I, you will play a pivotal role in the execution of clinical research projects.
The Opportunity
This is an exciting opportunity for a detail-oriented and organized individual to join our team as a Clinical Research Associate I.
Your key responsibilities will include:
* Serving as the primary point of contact for project teams and investigative sites
* Maintaining site performance and implementing corrective action plans as needed
* Assisting more senior CRAs with preparation for site visits and ensuring timely completion of tasks
* Reviewing Case Report Forms and generating queries to ensure data integrity
* Liaising with project teams to manage clinical trial supplies and ensure compliance with regulatory requirements
This role may require travel to conduct site visits or attend client or internal meetings as needed.
To be successful in this role, you will require a university degree in a life science or related field, or certification in a related allied health profession from an accredited institution.
A strong understanding of ICH-GCP and other applicable regulations/guidelines is also essential.
What We Offer
We offer a competitive compensation package and opportunities for professional growth and development.
Our team is dedicated to delivering high-quality results and making a positive impact on patient outcomes.
If you are a motivated and detail-oriented individual who is passionate about clinical research, we encourage you to apply for this exciting opportunity.