The Senior Clinical Trial Supplies Associate will perform administrative and support activities to help manage the logistics of clinical trial supplies, operating independently with minimal day-to-day oversight.

Job Responsibilities:

• Manage CSS Email Inbox
• Manage IRT system access for CSS, Logistics, Depots, Safety and Bioanalytics Users for all studies
• Assist in UAT testing when required
• Bi-yearly review of IRT system users for all studies
• Receive and triage requests for ancillary supplies compatibility review, forward to FDG for review
• Perform internet search and contact manufacturer for information
• Data entry of information into database (ASIST or spreadsheet) and Teams
• Detail and quality oriented

Qualification Requirements:

• Bachelor’s Degree (or equivalent) level of education, preferably in a related field or focused on life sciences
• Moderate experience (2+ years) in a contract research organization (CRO), pharmaceutical, or biotechnology company
• Strong knowledge of Good Clinical Practice, ICH guidelines, Good Manufacturing Practice, and other applicable regulatory requirements
• High level of competence in English language
• Ability to perform several tasks simultaneously to meet deadlines
• Self-motivation and ability to work independently
• High proficiency with MS Office Applications
• Ability to travel as necessary (up to 10%)

Benefits:

• Company car or car allowance
• Health benefits to include Medical, Dental and Vision
• Company match 401k
• Eligibility to participate in Employee Stock Purchase Plan
• Eligibility to earn commissions/bonus based on company and individual performance
• Flexible paid time off (PTO) and sick time

Salary Range:

$56,400.00 - $95,900.00

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