Moderna, Inc.

Clinical Trial Manager, Clinical Operations, Infectious Disease

Moderna, Inc.$109K — $174K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • At least 5 years of trial coordination experience in clinical research environments.
  • Advanced or Bachelor’s degree in a science-related field.
  • Experience in a global clinical setting.
  • Solid understanding of the drug development process.
  • Familiarity with FDA and ICH GCP guidelines.
  • Strong project management abilities.
  • Excellent verbal and written communication skills.

Responsibilities

  • Manage day-to-day operations of assigned clinical trial(s) to meet all deliverables.
  • Communicate with internal teams to ensure timelines and objectives are achieved.
  • Oversee the trial feasibility process from initiation.
  • Collaborate with Clinical Operations Lead and other Clinical Trial Managers on study execution.
  • Draft site materials such as training manuals and support documentation.
  • Monitor clinical data for timely entry and readiness for review.
  • Periodically review clinical data and reports for issues and compliance.

Benefits

  • Comprehensive healthcare coverage with additional voluntary benefit options.
  • Access to fitness, mindfulness, and mental health support resources.
  • Family planning benefits including fertility treatments and adoption support.
  • Generous paid time off with vacation, volunteer days, and sabbaticals.
  • Savings and investment plans for future financial security.
  • Location-specific perks to enhance the employee experience.
Full 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 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


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


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 $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.

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