As a Clinical Research Associate, you will be responsible for ensuring the rights and well-being of trial participants are protected and reported data are accurate and complete. You will be the primary contact between investigative sites, sponsors, and our organization.
Key Responsibilities:
* Ensure clinical trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and organizational SOPs.
* Build relationships with Principal Investigators, study coordinators, pharmacists, and other site personnel to manage clinical trials efficiently.
* Foster customer relationships to ensure focus on timely and productive project delivery.
* Collaborate with internal teams to prepare essential documents and support ethics and regulatory submissions.
* Develop and implement site-specific recruitment plans to ensure participant enrollment.
* Conduct monitoring visits, including site selection, initiation, monitoring, and close-out visits, as per ICH GCP.
Requirements:
* Graduate in a clinical or life sciences-related field.
* Relevant experience/qualifications in allied professions may also be considered.
* Good time management skills, attention to detail, ability to work well in a team, and computer literacy.
* Minimum 6 months of CRA independent monitoring experience (CRA II), 2+ years (CRA III), or 4+ years (SCRA) of independent monitoring experience.
Benefits:
* Hybrid working arrangements and flexible working hours to achieve work-life balance.
* Paid parental leave for both parents, flexible leave entitlements, wellness programs, and ongoing development programs.
Our Organization:
* We strive to create an inclusive workplace where everyone is treated fairly and with respect.
* We welcome applicants from diverse backgrounds, including those who identify as LGBTIQ+, have a disability, or have caring responsibilities.