Sr. Manager, Clinical Data Management

Moderna, Inc.
Cambridge, Massachusetts, United States
Full-time

The Role :

Moderna is seeking a Senior Manager, Clinical Data Management to work across its programs. This position will initiate best practices and lead clinical data management initiatives across the ventures as well as support the oversight of data management vendors and data handling.

This role will report to the Director, Clinical Data Management at Moderna

Heres What Youll Do :

Perform data management oversight activities in support of Moderna clinical studies; oversee the activities of CRO DM counterparts to ensure adherence to scope of work and service agreements, and to ensure deliverables are met in accordance to quality

Collaborate with clinical study teams and vendors to ensure project deliverables are met, including data acquisition, quality data review and reporting in compliance with GCP, SOPs and regulatory requirements

Participate in the development of all Data Management documentation including the Data Management Plan, CRF Completion Guidelines, Data Validation Specification, Data Transfer Specifications, etc.

Manage clinical trial data through review, cleaning, auditing, validation procedures and ensure data handling compliance with regulatory requirements

Review data analysis listings and report on performance and quality; review clinical data within studies and across for trend analysis

Perform thorough development testing of the eCRF prior to deployment, inclusive of User Acceptance Test (UAT) Plans, Test Scripts and execute testing applicable

Participate in the Data Standards Committee and act as the liaison between the study team members Rare Diseases to standardize data collection and reporting

Heres What Youll Bring to the Table :

Bachelors Degree in a science-based subject expertise.

At least 8 years of clinical data management experience in industry, with experience across indications and EDC platforms

Early and late development experience

Multi-faceted background devising plans for operational challenges such as site EDC training, preparing cohorts for data review in dose escalation, vendor oversight, protocol deviation management, data cleaning, etc.

Cross Collaboration proficiency with other functions such as Biostatistics, Statistical Programming, and Pharmacovigilance

Thorough command of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studies

Outstanding verbal and written communication skills, in addition to excellent organizational skills

Creative, capable problem-solver

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

  • Highly competitive and inclusive medical, dental and vision coverage options
  • Flexible Spending Accounts for medical expenses and dependent care expenses
  • Lifestyle Spending Account funds to help you engage in personal enrichment and self-care activities
  • Family care benefits, including subsidized back-up care options and on-demand tutoring
  • Free premium access to fitness, nutrition, and mindfulness classes
  • Exclusive preferred pricing on Peloton fitness equipment
  • Adoption and family-planning benefits
  • Dedicated care coordination support for our LGBTQ+ community
  • Generous paid time off, including :

Vacation, sick time and holidays

Volunteer time to participate within your community

Discretionary year-end shutdown

Paid sabbatical after 5 years; every 3 years thereafter

  • Generous Paid Leave offerings, including 18 weeks of 100% paid parental leave for all new parents
  • 401k match and Financial Planning tools
  • Moderna-paid Life, LTD and STD insurance coverages, as well as voluntary benefit options
  • Complimentary concierge service including home services research, travel booking, and entertainment requests
  • Free parking or subsidized commuter passes
  • Location-specific perks and extras!

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)

5 days ago
Related jobs
Promoted
Moderna, Inc.
Cambridge, Massachusetts

The Senior Clinical Trial Manager (Sr. Review clinical data to ensure timely entry and readiness for data review meetings. Review and provide clinical operations input into relevant clinical documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other...

Promoted
Promote Project
Waltham, Massachusetts

Reporting to the Director, Data Management, you will be responsible for overseeing all clinical data management and related deliverables from start-up through close out of various clinical trials. Responsible for relationships with Data Management partners (eg, CROs and vendors) from protocol develo...

Promoted
Cardurion Pharmaceuticals, Inc
Burlington, Massachusetts

Devises efficient, effective clinical trial execution strategies; guides planning and execution of clinical studies, including management of study budgets / timelines and external vendor(s) management. May serve as a line manager to one or more Clinical Trial Managers (CTMs) and/or Clinical Trial As...

Promoted
Aura Biosciences
Boston, Massachusetts

Clinical Trial Manager will be responsible for managing various aspects of clinical trial conduct with subject matter experts including clinical development, contract vendors, and regulatory to achieve clinical trial goals on time and within budget. Partnering closely with the cross-functional stake...

Innova Solutions
Cambridge, Massachusetts

Oversee, develop and maintain study-specific documentation, including Data Management Plans, eCRF specifications, CRF Completion Guidelines, Data Validation Guidelines, Data Transfer Specifications, Coding Guidelines, Post Production Database Change Control Documentation, Database Audit and Lock Pro...

Takeda Pharmaceuticals
Cambridge, Massachusetts

While the Clinical Data Standards provides the standards for clinical operation and data flow, the Clinical Data Engineering team drives the data architecture for clinical data. The Clinical Data Sciences comprises of the Clinical Data Engineering and Clinical Data Standards. The Clinical Data Scien...

MFS Investment Management
Boston, Massachusetts

For a leading and rapidly growing Asset Management firm, the Investment Data Management Office champions a long-term, strategic initiative to unify and harmonize our investment data. The Investment Data Product Owner works with the Head of Investment Data Management and Director of Product to transl...

ONO PHARMA USA
Cambridge, Massachusetts

Manager level role that utilizes the clinical development strategy to determine the efficacy and safety of candidate drug products in clinical development based on the interpretation of trial results. Monitors and evaluates clinical data as a basis for the development and design of the clinical drug...

Capital One
Cambridge, Massachusetts

As the Senior Manager of Technical Program Management in Capital One’s Enterprise Data and Machine Learning (EDML) division, you’ll be at the forefront of driving innovation and efficiency in our Data API ecosystem. Center 3 (19075), United States of America, McLean, VirginiaSenior Manager, Technica...

Clinical Dynamix
Boston, Massachusetts

Reporting to the Senior Director, Clinical Data Management, the Associate Director, Clinical Data Management will define and lead the clinical data management strategy for the organization. Organize and direct the initial stage of the studies, review and sign off on various items such as eCRF, data ...