More Information
- Reference number 1/04/2025
- Location In Poland
- The form of work hybrid work
- Working hours full-time
- Experience level required 2 lata – 5 lat
- Student status student
-
Requirements
All candidates must already have legal authorization to work in Poland in order to be considered.
Here’s What You’ll Need (Minimum Qualifications):
- Current enrollment in or recent completion of an undergraduate (Second Year or later) or graduate program (any year) focused on Pharmacy, Medicine, Biology, Life Sciences, or similar field
-
Competences sought
Here’s What You’ll Bring to the Table (Preferred Qualifications):
- A passion for innovation and the potential of mRNA technology to transform medicine.
- Strong attention to detail and ability to manage multiple tasks effectively.
- A proactive and self-motivated attitude, with the flexibility to adapt to a dynamic environment and the demonstrated ability to reach out and coordinate across teams to get necessary information.
- Excellent communication and collaboration skills
- An eagerness to learn, grow and constructively challenge the status quo in pursuit of excellence
- Fluency in English required
- A team-oriented mindset with a willingness to take ownership of assigned tasks and contribute meaningfully to team goals.
- Familiarity with the drug development process (technical, non-clinical, clinical) a plus
- A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative.
-
Scope of duties
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 a Pharmacovigilance intern, you will work closely with our Pharmacovigilance team and cross-functional partners to ensure the safety of Moderna’s investigational and approved products and maintain compliance with global regulatory requirements. This internship provides the unique opportunity to understand the important role Pharmacovigilance plays in biotechnology and pharmaceutical companies, as well as to gain experience as part of a fast-paced and innovative environment.
This internship is expected to be 11 weeks in duration (40 hrs/week) from July 1 – Sep 12. The internship will be located in Moderna's Warsaw office, with an expectation of working at least 70% in-office.
Here’s What You’ll Do:
Under the supervision and guidance of the Pharmacovigilance team, you will:
- Assist in processing Individual Case Safety Reports (ICSRs) from Moderna’s clinical trials and post-marketing sources, ensuring data accuracy and completeness.
- Support the preparation and submission of global safety reports, including expedited regulatory submissions.
- Participate in quality assurance activities to enhance the accuracy and consistency of pharmacovigilance data.
- Contribute to cross-functional collaborations with medical review, regulatory affairs, and digital teams to optimize safety monitoring processes.
- Gain exposure to pharmacovigilance systems and tools used for data collection, signal detection, and adverse event reporting.
- Support execution of digital initiatives and demonstrate a “Digital First” mindset to enhance engagement and streamline processes
- Attend relevant meetings and contribute to discussions to gain insight into the role of Pharmacovigilance professionals in a biotech setting
-
Employment conditions offered
The internship is paid and comes with the relevant benefits for fixed-term employment contracts.
The interns will also be part of the inaugural Summer Intern program at our Warsaw office, and will benefit from mentorship, leadership exposure, and networking opportunities throughout their summer experience.
- Number of wanted persons 2
