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Clinical Trial Manager, Clinical Operations, Infectious Disease

Moderna

Clinical Trial Manager, Clinical Operations, Infectious Disease

full-timePosted: Aug 25, 2026Updated: Sep 1, 2026Massachusetts, Cambridge

Job Description

The Role:The Clinical Trial Manager provides clinical trial oversight to the assigned clinical trial(s) ensuring deliverables are met in terms of quality, compliance and timing. Strong vendor management is critical for this role. external vendors and CROs.The position reports to the Director, Clinical Operations and is accountable to the Clinical Operations Lead for assigned studies.This role may work collaboratively on one trial or across several trials to support clinical operations activities.Here’s What You’ll Do:Day to day management of assigned clinical trial(s) to ensure deliverables are met in all phases of trialCommunication to internal team members on deliverables and ensuring timelines are metManage trial feasibility processWork closely with study Clinical Operations Lead and/or assigned Clinical Trial Manager(s) to execute clinical studiesDrafting site materials including training, manuals and support documentationMonitoring of clinical data to ensure timely entry and readiness for data review meetingsPeriodic review of clinical dataReview of clinical monitoring reports to ensure timely completion and identification of issuesEnsure trial samples are ready to be sent to vendors in order to meet trial deliverablesMaintain trial metricsEnsure trial is conducted in accordance with Moderna and ICH/GCP standards including multiple regions in global trialsSupport testing clinical trial systems/databases (i.e. UAT)May support additional clinical trial(s) in an unblinded Clinical Trial Manager capacityDevelop and maintain strong, collaborative relationships with key stakeholders within ModernaHere’s What You’ll Bring to the Table:At least 5 five years of trial coordination experience in a clinical research and industry environmentAdvanced degree preferred or Bachelor’s in a science-based subjectRelevant experience in global settingSolid understanding of drug developmentGood project management skillsGood understanding of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studiesExcellent verbal and written communication skillsGood organizational skills and attention to detailPay & BenefitsAt 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 needsA holistic approach to well-being, with access to fitness, mindfulness, and mental health supportFamily planning benefits, including fertility, adoption, and surrogacy supportGenerous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdownSavings and investments to help you plan for the futureLocation-specific perks and extrasThe salary range for this role is $109,200.00 - $174,600.00. 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 ModernaSince 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 of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Our Working Model 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. Moderna is a smoke-free, alcohol-free, and drug-free work environment. Equal OpportunitiesModerna 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 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 an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. AccommodationsWe’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can 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. #LI-TR2-

Locations

  • Massachusetts, Cambridge
  • Clinical Development
  • Bethesda - USA - MD
  • Maryland, Bethesda

Skills Required

  • clinical researchintermediate
  • global settingintermediate

Required Qualifications

  • At least 5 five years of trial coordination experience in a clinical research and industry environment (experience)
  • Advanced degree preferred or Bachelor’s in a science-based subject (degree in bachelor)
  • Relevant experience in global setting (experience)
  • Solid understanding of drug development (experience)
  • Good project management skills (experience)
  • Good understanding of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studies (experience)
  • Excellent verbal and written communication skills (experience)
  • Good organizational skills and attention to detail (experience)
  • At least 5 five years of trial coordination experience in a clinical research and industry environment (experience)
  • Advanced degree preferred or Bachelor’s in a science-based subject (degree in bachelor)
  • Relevant experience in global setting (experience)
  • Solid understanding of drug development (experience)
  • Good project management skills (experience)
  • Good understanding of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studies (experience)
  • Excellent verbal and written communication skills (experience)
  • Good organizational skills and attention to detail (experience)

Responsibilities

  • Day to day management of assigned clinical trial(s) to ensure deliverables are met in all phases of trial
  • Communication to internal team members on deliverables and ensuring timelines are met
  • Manage trial feasibility process
  • Work closely with study Clinical Operations Lead and/or assigned Clinical Trial Manager(s) to execute clinical studies
  • Drafting site materials including training, manuals and support documentation
  • Monitoring of clinical data to ensure timely entry and readiness for data review meetings
  • Periodic review of clinical data
  • Review of clinical monitoring reports to ensure timely completion and identification of issues
  • Ensure trial samples are ready to be sent to vendors in order to meet trial deliverables
  • Maintain trial metrics
  • Ensure trial is conducted in accordance with Moderna and ICH/GCP standards including multiple regions in global trials
  • Support testing clinical trial systems/databases (i.e. UAT)
  • May support additional clinical trial(s) in an unblinded Clinical Trial Manager capacity
  • Develop and maintain strong, collaborative relationships with key stakeholders within Moderna
  • Day to day management of assigned clinical trial(s) to ensure deliverables are met in all phases of trial
  • Communication to internal team members on deliverables and ensuring timelines are met
  • Manage trial feasibility process
  • Work closely with study Clinical Operations Lead and/or assigned Clinical Trial Manager(s) to execute clinical studies
  • Drafting site materials including training, manuals and support documentation
  • Monitoring of clinical data to ensure timely entry and readiness for data review meetings
  • Periodic review of clinical data
  • Review of clinical monitoring reports to ensure timely completion and identification of issues
  • Ensure trial samples are ready to be sent to vendors in order to meet trial deliverables
  • Maintain trial metrics
  • Ensure trial is conducted in accordance with Moderna and ICH/GCP standards including multiple regions in global trials
  • Support testing clinical trial systems/databases (i.e. UAT)
  • May support additional clinical trial(s) in an unblinded Clinical Trial Manager capacity
  • Develop and maintain strong, collaborative relationships with key stakeholders within Moderna

Benefits

  • general: 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.
  • general: Competitive healthcare, plus voluntary benefit programs to support your unique needs
  • general: A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • general: Family planning benefits, including fertility, adoption, and surrogacy support
  • general: Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • general: Savings and investments to help you plan for the future
  • general: Location-specific perks and extras

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