New · posted Nov 1
Moderna · Biotechnology
Cluster Lead, Pharmacovigilance, LATAM
- Cambridge, MA
- On-site
- Full-time
- Manager
The role
ModernaTX, Inc. seeks a Cluster Lead, Pharmacovigilance, LATAM for its Cambridge, Massachusetts location.
What you need
Minimum requirements
- Requires a Master’s degree or foreign equivalent in Pharmaceutical Sciences or a related field and 8 years of experience as a Pharmacovigilance Lead, Senior Pharmacovigilance/Drug Safety Specialist, or related position supporting pharmacovigilance operations.
- Alternatively, employer will accept a Bachelor’s degree, or foreign equivalent, in the fields specified and 10 years of specified progressive, post-baccalaureate experience.
- 8 years of experience must include:
- Pharmacovigilance oversight and regulatory engagement for the LATAM region applying Good Pharmacovigilance Practices for the Americas and local PV regulations for Mexico, Argentina, Brazil, Paraguay, Colombia, Panama, Peru and Chile;
- Individual Case Safety Report (ICSR) processing, aggregate safety reporting, Pharmacovigilance Quality Management Systems, and compliance;
- Ensuring timely and accurate safety data management, maintaining robust quality systems, and aligning regional LATAM pharmacovigilance operations with global regulatory standards;
- Working with Contract Research Organizations (CROs), vendors, business partners and stakeholders across cross-functional teams to ensure aligned pharmacovigilance operations;
- Veeva Safety and Argus; Risk Management Plans (RMP), Periodic Safety Updated Reports (PSUR), and development of Standard Operating Procedures (SOPs) and Pharmacovigilance Agreements (PVA); and
- Pharmacovigilance Management for business partners and vendors.
- Position requires up to 15% domestic and international travel, fully reimbursed.
The salary range for this role is $167,000.00 to $300,700.00. This range reflects the lowest to highest salary we, in good faith, believe we would pay for this role at the time of this posting. The minimum target pay for this particular position, based on its primary location, is $243,000.00 to $300,700.00. An individual’s placement within the range will depend on several factors, including but not limited to specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs.
Worksite: 325 Binney Street, Cambridge, Massachusetts, 02142, United States
For summary of benefits and to apply visit https://modernatx.wd1.myworkdayjobs.com/en-US/M_tx (Job ID: R19967) or email resume and cover letter to [email protected] with subject line: R19967.
What you'll do
Here’s What You’ll Do
- Responsible for end-to-end oversight of pharmacovigilance (PV) operations across multiple Latin American countries, including the implementation and continuous improvement of PV systems to ensure compliance with local and international regulatory requirements.
- Provide dynamic leadership and strategic oversight of PV operations in Latin America, ensuring excellence in execution, and define the PV strategy for the region and develop actionable short-, medium-, and long-term plans to achieve safety and compliance goals.
- Engaging with local Health Authorities to understand, interpret, and align Moderna’s safety reporting processes with country-specific legislation, particularly in a region where regulatory frameworks are actively evolving.
- Establish governance and operational processes with business partners and vendors, including the development of safety data exchange agreements and procedures for case processing, reconciliation, and audit preparedness.
- Regularly coordinate with global teams to ensure the exchange of safety information meets internal standards and regulatory expectations.
- Develop and review Risk Management Plans (RMPs), Periodic Safety Update Reports (PSURs/PBRERs), and local literature screening strategies.
- Collaborate with cross-functional internal teams such as Regulatory Affairs, Commercial, and Clinical Development to ensure PV is embedded throughout the product lifecycle.
- Deliver cross-divisional projects that strengthen collaboration with global teams and support corporate safety objectives.
- Ensure full regional compliance with PV reporting requirements and regulatory expectations.
- Lead PV inspection readiness efforts and participate in internal audits and external inspections by partners and health authorities.
- Maintain and continuously improve a robust PV Quality Management System and Business Continuity Plan.
- Oversee the performance and compliance of vendors and partners executing PV activities on behalf of Moderna across the region.
- Engage with external stakeholders to benchmark and implement best practices in pharmacovigilance.
- Participate in regional safety vendor qualification, internal and external audits, and quality management activities to uphold safety and compliance standards.
Pay
$167,000 – $300,700 a year
Employer providedWhere you'll work
Cambridge, MAOn-siteOpen in Maps (opens in a new tab)
More jobs in Cambridge, MA
From the posting
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.
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.
Equal opportunity, accessibility and legal noticesModerna's statements, word for word
Equal Opportunities
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 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 an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Accommodations
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 [email protected].
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Job intelligence
The context around this role
Live data · November 1, 2026
Salary intelligence
How the pay compares
This role's midpoint is 41% above the US median for Clinical Safety & Pharmacovigilance roles at this level.
This roleEmployer provided
Manager roles in Massachusetts6 roles publishing pay
Manager roles in the US26 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $167,000 | — | $300,700 |
| Massachusetts (middle half) | $154,750 | $169,250 | $175,125 |
| All US (middle half) | $151,000 | $165,750 | $179,875 |
This role: Moderna's own published range. Comparisons: the base pay employers published on open Clinical Safety & Pharmacovigilance roles at the same level on Regulatory Jobs, November 1, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Safety & Pharmacovigilance
The general path across 162 open Clinical Safety & Pharmacovigilance roles on Regulatory Jobs, with the titles they carry most. Not Moderna's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 22 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership9
- GMP and compliance8
- Quality systems and risk4
- Documentation and SOPs3
- Regulatory submissions2
- Clinical trial conduct2
- Validation and qualification1
- Data and digital systems1
Company hiring pulse
Moderna on Regulatory Jobs
- 22
- Open roles
- 17
- Distinct roles
- 2
- Locations
By discipline
- Quality11 50%
- Regulatory8 36%
- Clinical3 14%
By level
- Associate & Specialist10 45%
- Director7 32%
- VP & Executive2 9%
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Cluster Lead, Pharmacovigilance, LATAM at Moderna
Open until filled. $167K–$301K a year, employer provided.