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Home Side Hustle Jobs eTMF Manager

Salary Unstated

eTMF Manager

Apply Now
Full-time Remote 37d ago

Location:

Cambridge, MA, US

Company:

Moderna Services, Inc. focuses on pioneering mRNA technology to develop transformative medicines.

Summary:

As an eTMF Manager, you will lead TMF operations and ensure compliance with regulatory requirements for clinical trials. Candidates should have a relevant Master's degree and several years of experience in clinical management.

Requirements:

Hard Skills: TMF Operations, Clinical Trial Management, Regulatory Compliance, eTMF Document Management, Quality Control

Credentials: Master’s degree in Biology, Pharmacy or related field, Bachelor’s degree in Biology, Pharmacy or related field

Experience: 3 years of experience in the position offered or as a TMF Lead, Specialist, Coordinator, or related position within the pharmaceutical and biotech industry, 3 years of experience applying U.S. and international regulatory requirements for TMF, 3 years of experience working with specialist functions within clinical trial teams, 3 years of experience collaborating with clinical trial teams and vendors, 3 years of experience providing TMF inspection readiness data and analysis, 2 years of eTMF document management experience

Job Description:

The Role: 

Moderna Services, Inc. seeks an eTMF Manager for its Cambridge, Massachusetts location.

Here’s What You’ll Do: 

  • Apply U.S. and international regulatory requirements to lead the execution of TMF Operations processes and strategy, and assist with establishing and maintaining TMF monitoring and reporting for clinical trials. 

  • Maintain effective communication with clinical study teams, Contract Research Organization (CRO) staff, and eTMF vendor personnel throughout study start-up, maintenance, and close-out.

  • Work with cross-functional study teams and partners to help analyze vendor system and process changes and impact to applicable internal processes. 

  • Support TMF document filing into Moderna eTMF system, performs quality checks of documents uploaded and respond to inquiries regarding TMF management and contents.

  • Author study TMF plans, TMF Indexing, work instruction manuals, data capture guidelines and standard operating procedures.  

  • Deliver Key Performance Indicator (KPI) reports, eTMF reports to the study team, manage expectations, track ongoing KPI across the study team in conjunction with the Clinical Trial Managers and Clinical Project Leads, and monitor the TMFs for completeness and trends. 

  • Support system updates by participating in user acceptance testing and system enhancement discussions. 

  • Complete other TMF document-related tasks as required by the study teams or functional groups in Clinical Development Operations. 

  • Drive and support portfolio-level initiatives including process change, management, and development.  

  • Mentor and provide high-level oversight of junior TMF positions within assigned portfolio.

  • Provide process subject matter expertise and support for TMF creation, maintenance, closure, and transfer per company and CRO Standard Operating Procedures (SOPs) and standards. 

  • Support CRO and partnership migration and integration activities, TMF reporting and compliance.

  • Provide best practice guidance and support to ongoing and ad-hoc TMF projects and initiatives.

  • Provide process and planning support to the Clinical Trial Managers and Clinical Project Leads for TMF related remediation and process execution as needed. 

  • Support integration of partnered or acquired clinical information including transfer of TMFs in compliance with applicable regulations and best practices. 

  • Proactively stay current with best practices and recommend applications across portfolios to continuously improve TMF operations processes. 

  • Lead projects in support of study or portfolio TMF objectives and attend standing cross-functional meetings.

  • May telecommute 100% from anywhere in the U.S.

Here’s What You’ll Bring to the Table:

Minimum requirements: 

  • Requires a Master’s degree in Biology, Pharmacy or related field and 3 years of experience in the position offered or as a TMF Lead, Specialist, Coordinator, or related position within the pharmaceutical and biotech industry. Alternatively, Employer will accept a Bachelor’s degree in the stated fields and 5 years of progressive, post-baccalaureate experience in the stated positions.

  • Must have 3 years of experience with the following:

  • Applying U.S. and international regulatory requirements for TMF used in submission of a new drug approval;

  • Working with specialist functions within clinical trial teams to advise on acceptable records of clinical trial conduct;

  • Collaborating with clinical trial teams and vendors to resolve conflicts and escalate issues;

  • Providing TMF inspection readiness data and analysis to trial teams and management; and

  • Performing quality checks on documents to resolve high risk document issues.

  • Must have 2 years of eTMF document management experience. 

  • May telecommute 100% from anywhere in the U.S.

  • Apply at https://modernatx.wd1.myworkdayjobs.com/en-US/M_tx (Job ID: R17746) or email resume and cover letter to careers@modernatx.com with subject line: R17746.

#DNI

At Moderna, we believe that when you feel your best, you can do your best work.  That’s why our US benefits and global well-being resources are designed to support you—at work, at home, and everywhere in between.

  • Best-in-class healthcare coverage, plus a suite of voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Lifestyle Spending Accounts to personalize your well-being journey
  • Family planning and adoption benefits
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investment opportunities
  • Location-specific perks and extras

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. 

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 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 consider qualified applicants regardless of criminal histories, consistent with legal requirements. 

We’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.  (EEO Employer)  

Apply Now

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