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Specialist, Global Case Management

extra holidays - extra parental leave
Remote: 
Full Remote
Contract: 
Experience: 
Junior (1-2 years)
Work from: 

Offer summary

Qualifications:

University degree in Pharmacy or Medicine, Minimum 1 year experience in drug safety, Medical Writing experience preferred, Proficient in Argus and MS Office.

Key responsabilities:

  • Review and document case-related information
  • Write narratives describing adverse events
Moderna  logo
Moderna Biotech: Biology + Technology Large https://www.modernatx.com/
1001 - 5000 Employees
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Job description

The Role:

Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.

As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide contributing to global health initiatives. Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience with the potential to make a significant impact on patients' lives worldwide.

Moderna is solidifying its presence within our international business services hub in Warsaw, Poland, a city renowned for its rich scientific and technological heritage. This hub providescritical functions, meeting the growing demand of Moderna’s global business operations. We're inviting professionals from around the world to join our mission and

contribute to the future of mRNA medicines​.

This role will support Moderna's clinical trials by ensuring timely and accurate

processing of Individual Case Safety Reports (ICSRs). You will focus on triaging, writing detailed narratives, and quality controlling adverse event data, directly impacting our

pharmacovigilance practices and commitment to patient safety.

Here's What You'll Do:

Your key responsibilities will be:

  • Review, rank, verify, process, and document case-related information, including event terms, seriousness, timelines, and consistency.

  • Write comprehensive narratives describing adverse events using source documents.

  • Ensure compliance with applicable regulations, guidelines, and company standards in safety data processing.

Your responsibilities will also include:

  • Perform triage and quality control of ICSRs.

  • Contribute to training and mentoring new colleagues.

  • Support inspection readiness activities and represent CS&PV at interdepartmental meetings.

  • Manage multiple tasks and prioritize competing requests or projects.

  • Escalate issues to management as needed and participate in continuous improvement opportunities.

The key Moderna Mindsets you’ll need to succeed in the role:

  • We obsess over learning: This role requires meticulous attention to detail and the ability to adapt quickly to evolving regulations and internal procedures, ensuring the highest quality of work.

  • We behave like owners: The Specialist will take full accountability for accurate case processing and narratives, reflecting our organizational commitment to excellence in global case management​.

Here's What You'll Nee:

  • University degree in Pharmacy/Medicine or other relevant life sciences discipline (Dentistry, Experimental Medicine, Microbiology, Veterinary, Biotechnology, Physiotherapy, Medical Biology or similar)

  • Minimum 1 year of experience in drug safety/pharmacovigilance case processing

  • Medical Writing experience preferred

  • Argus safety database and other platforms MS Office suite, Excel, Powerpoint, Visio

  • Effective time management skills

  • Excellent communication skills (verbal and writing); results oriented and strong attention to detail

  • Fluency in English required

  • This role is expected to be in office 70% of the time with flexibility to work from home up to 30%.

Moderna offers personalized benefit programs and well-being resources as unique as our global workforce so employees can do their best work.

We recognize and appreciate your diverse needs and interests and do our best to support you at work and at home with:

  • Quality healthcare and insurance benefits
  • Lifestyle Spending Accounts to create your own pathway to well-being
  • Free premium access to fitness, nutrition, and mindfulness classes
  • Family planning and adoption benefits
  • Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, and a discretionary year-end shutdown
  • Educational resources
  • Savings and investments
  • Location-specific perks and extras!

The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

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. 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. We’re 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 or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment 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 and Adjustments team at leavesandaccommodations@modernatx.com.

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Required profile

Experience

Level of experience: Junior (1-2 years)
Industry :
Biotech: Biology + Technology
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Detail Oriented
  • Microsoft Office
  • Microsoft Excel
  • Microsoft PowerPoint
  • Time Management
  • Communication
  • Results Focused

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