Senior Manager, Clinical Supplies Systems

The Role:

Moderna is seeking a Senior Manager, Clinical Supplies Systems to oversee and manage IRT systems for Modernas growing portfolio of studies. This person will be required to work with external IRT vendors (day-to-day operations and leadership capacity) to ensure Modernas clinical portfolio aligns with internal stakeholders and timelines from business. This position will work collaboratively and cross-functionally to gather relevant requirements and utilize the available resources to create the IRT system design, provide subject matter expertise, and ensure expert and on-time IRT system delivery and implementation. The successful candidate is a subject matter expert at IRT-related integrations, imaginative, skilled at understanding the needs of a clinical development operations organization with high attention to detail, a collaborative outlook, a positive leader, above no task, and the ability to pursue multiple options in parallel to meet project timelines 100% of the time. Forecasting applications and IRT product management background are a plus. Senior Managers are expected to independently manage programs and studies, contributing their expertise in IRT system management. Senior Managers are anticipated to operate autonomously serving as a calming & key face of our organization with a goal of ensuring the IRT team brand is well represented, with the Associate Director/Director serving as the primary contact for risk mitigation and issue escalation.

Heres What Youll Do:

Under the guidance of an Associate Director or Director, manage IRT Systems for multiple programs and studies at Moderna with autonomy

Responsible for IRT oversight, day-to-day vendor management, implementation project management, IRT requirements and design, user acceptance testing, and maintenance

May be responsible for mentoring Clinical Supply Systems Specialists

Responsible for facilitation of IRT technical support, data changes, and working with Clinical Operations and Monitoring to achieve their goals

Responsible for UAT test case creation, oversee and facilitate signatures on documentation, and risk and impact assessment creation, etc.

Adheres to processes and ensure compliance to relevant SOPs

Responsible for administration and uploading documentation to appropriate eTMF

Collaborates cross-functionally to schedule projects, end-user training, meetings, and discussions

Deliver exceptional customer service and technical support to Clinical Operations, Biostatistics, Clinical Supplies, and Data Management under the directive of the Associate Director or Director

Serve as IRT Subject Matter Expert to other Moderna departments

Task assignments may expand in scope based on the individual's level of experience

May be asked to participate in internal audits or external inspections

Productively contribute or lead process updates, cross-functional initiatives, standards documentation updates, and/or SOPs

May serve as business or product owner for internal applications that are IRT adjacent, such as forecasting, enrollment planning, and/or centralized clinical inventory and distribution system.

Heres What Youll Bring to the Table:

At least five to eight years of clinical supply systems experience

Bachelors degree in a science-based subject (advanced degree preferred)

Prior Product Ownership Experience (strongly preferred)

Prior demonstration of innovation as it relates to integrations between clinical systems (IRT, EDC, etc.) in a clinical research environment

Understanding of Cold Chain distribution and the effect on IRT

IRT Subject Matter Expertise

Creative, capable problem-solver

Experience in establishing and maintaining relationships with vendors

Working knowledge of ICH, GAMP, FDA, IRB/IEC and other applicable regulations/guidelines and demonstrated understanding of clinical research protocol requirements

Demonstrated proficiency with word processing, spreadsheet, database, presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, and SharePoint)

Successful candidate will be curious in exploring new path for clinical research, bold in proposing creative solutions and ideas. Will work collaboratively with multifunctional teams and partners and will be relentless in pursuing successful outcomes

Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including:

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, theinfrastructure 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 peopleare 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.

As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute and make a meaningful impact.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Moderna is a smoke-free, alcohol-free and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply

Moderna is proud to be an equal opportunity workplace and is an affirmative action employer.

Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is an E-Verify Employer in the United States. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Belonging, Inclusion, and Diversity are critical to the success of our company and our impact on society. Were focused on attracting, retaining, developing, and advancing our employees and believe that by cultivating diverse experiences, backgrounds, and ideas, we can provide an environment where every employee is able to contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at leavesandaccommodations@modernatx.com. (EEO/AAP Employer)

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