Clinical Trial Associate, Clinical Operations

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he Role The Clinical Trial Associate (CTA) provides clinical trial coordination support to project teams for assigned clinical trial(s). This support includes tracking a wide range of key operational activities and maintaining essential study documentation, including the electronic Trial Master File (eTMF). This position works closely with internal team members, external vendors, CROs, and clinical sites to support the successful execution of clinical studies. The CTA will collaborate cross-functionally to ensure clinical operations activities are conducted efficiently, compliantly, and in alignment with study objectives. Successful candidates may be aligned to support clinical programs in Infectious Disease, Oncology, or other therapeutic areas based on business needs and experience. Here's What You'll Do Assist Clinical Operations Leads (COLs) and/or Clinical Trial Managers (CTMs) with the day-to-day operational activities of assigned clinical trials to ensure study objectives and timelines are met with quality and in compliance with applicable SOPs and regulatory guidelines. Maintain clinical trial files (including eTMF), project processes, tracking systems, and other study or departmental systems. Liaise with Clinical Sample Management to support the tracking and coordination of biomarker and clinical sample testing with external laboratories. Collaborate with Clinical Data Management and Digital Informatics to ensure timely training and access to clinical systems (e.g., EDC, IWRS, ePRO, eTMF) for external stakeholders, including CRO personnel and clinical site staff. Coordinate project team and departmental meetings, including preparation and maintenance of meeting documentation and action items. Assist with vendor and clinical site agreements, budget tracking, purchase order management, invoice reconciliation, and related operational activities. Develop and maintain strong, collaborative relationships with internal stakeholders, CROs, vendors, and clinical sites. Support inspection readiness activities and contribute to continuous process improvement initiatives within Clinical Operations. Here's What You'll Need (Basic Qualifications) Minimum of 2 years of experience in a clinical research or clinical operations environment. Bachelor's degree in a science-related discipline preferred. Basic understanding of drug development and clinical trial conduct, including familiarity with FDA regulations, ICH-GCP guidelines, and industry best practices. Strong verbal and written communication skills. Excellent organizational skills and attention to detail. Ability to manage multiple priorities in a fast-paced environment. Self-motivated, adaptable, and eager to learn. Demonstrated ability to collaborate effectively across functions and with external partners. Pay & Benefits At Moderna, we believe that when you feel your best, you can do your best work. That's why our benefits and well-being resources are designed to support you-at work, at home, and everywhere in between. Competitive healthcare, plus voluntary benefit programs to support your unique needs A holistic approach to well-being, with access to fitness, mindfulness, and mental health support Family planning benefits, including fertility, adoption, and surrogacy support Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown Savings and investments to help you plan for the future Location-specific perks and extras The salary range for this role is $74,000.00 - $118,400.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual's position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs. The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance. About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities. We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. If you want to make a difference and join a team that is changing the future

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