Trial Coordinator Associate

We strive to unite caring with discovery to make life better for people around the world. Our team is dedicated to discovering and bringing life-changing medicines to those who need them, improving the understanding and management of disease, and giving back to our communities through philanthropy and volunteerism. We're looking for individuals determined to make a positive impact on people's lives.

• Coordinate trial activities including collection and submission of regulatory documents, negotiation of informed consent documents, serve as the point of contact for investigator sites and ensure site compliance to required training
• Communicate effectively with investigator sites to enable start-up and maintain an active collaboration during maintenance and close-out
• Collaborate with internal and external parties to enable active collaboration during site activation, maintenance and close-out
• Develop and manage budgets for investigator sites
• Manage financial transactions related to investigator payments and other expenses
• Identify, communicate and resolve issues that may arise during trials
• Coordinate the delivery of clinical trial materials
• Oversee the translation process for clinical trial documents and ensure quality control
• Populate systems to track trial performance and site activity
• Maintain inspection readiness for regulatory documents and processes

We are committed to creating an inclusive environment where individuals with disabilities can actively engage in the workforce. If you require accommodation to submit your application, please complete the accommodation request form. Please note this is for individuals requesting an accommodation as part of the application process and any other correspondence will not receive a response.

We do not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.