Clinical Trial Associate

This is a fully remote position, open to applicants in France.

📋 Description

• Assist in the initiation and activation processes for sites.

• Oversee payments to investigator sites and manage invoicing tasks.

• Create Requests for Invoice (RFIs) based on extracted data from patient visits.

• Work in partnership with investigator sites and Clinical Research Associates (CRAs) to address payment and invoicing concerns.

• Establish and uphold site payment records within relevant systems.

• Administer and monitor site payments, ensuring both accuracy and compliance.

• Track payment schedules and follow up on pending invoices and inquiries.

• Guarantee compliance with financial protocols and specific payment stipulations associated with studies.

• Monitor invoice progress, track payment schedules, and proactively tackle any unresolved issues.

⛳️ Requirements

• A bachelor's degree in life sciences or a closely related discipline.

• Prior experience in clinical research or regulatory affairs is preferred but not mandatory.

• Exceptional attention to detail along with strong organizational abilities.

• Outstanding communication and interpersonal skills, capable of effective collaboration with cross-functional teams.

• Ability to work autonomously and juggle multiple responsibilities in a dynamic environment.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-based incentives.

• Health and wellness programs, which may include medical, dental, and vision insurance.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career progression pathways.