Compliance Monitoring & Reporting - Manager

PwC; Buenos Aires; Remote; ARS 68,155,000 - 98,446,000; Full time

Job summary

IQVIA in LatAm is seeking a Regulatory Reporting Specialist (Pharmacovigilance) to support submissions to regulatory authorities. The role spans data processing, compliance with SOPs, and cross‑functional collaboration across teams in Brazil and Argentina. Fluency in English, Spanish and Portuguese is required, with home-based work options.

The position emphasizes accuracy, timely case tracking, and teamwork with the operations and regulatory teams to ensure safe and compliant reporting.

Qualifications

• Bachelor's degree in life sciences.
• Languages: advanced English, Spanish and Portuguese.
• 1 year of pharmacovigilance experience (mandatory).
• Experience with Argus is desirable.
• Good knowledge of medical terminology and safety databases.

Responsibilities

• Process safety data according to regulations and SOPs.
• Ensure quality, productivity and timely delivery per project requirements.
• Track cases within the project plan.
• Identify and report quality problems to senior team members.
• Liaise with cross-functional teams and healthcare professionals to address issues.
• Attend project meetings and provide feedback to operations management.

Skills

Pharmacovigilance

English

Spanish

Portuguese

ARGUS

Education

Life sciences degree

Tools

Argus

Job description

**Job Requisition ID #**

26WD

**Position Overview**

The Manager, License Compliance, leads efforts to protect Autodesk's intellectual property by ensuring customers operate within licensing agreements. This role spans strategic planning, audit execution, customer engagement, and cross‑functional orchestration. Managers at all levels drive resolution of non‑compliance, influence go‑to‑market strategy and align compliance actions with revenue growth objectives.

**Responsibilities**

+ Oversee telemetry analysis, audit preparation, and resolution workflows.Ensure timely and accurate handling of compliance cases across customer segments.Monitor pipeline health and maintain data integrity across systems

+ Lead customer communications from operational to executive levels.Deliver complex compliance findings and negotiate resolutions.Tailor messaging stakeholder needs and licensing complexity

+ Coach and develop compliance teams across geographies and levels.Build onboarding, training, and succession plans.Foster a culture of accountability, trust, and continuous improvement

+ Allocate resources based on strategic priorities and team capacity.Manage staffing plans and coordinate cross‑functional support.Ensure readiness for high‑value engagements and escalations

+ Own compliance‑driven revenue forecasting across teams and regions.Integrate compliance forecasts into GTM and financial planning.Identify risks and opportunities to inform strategic decisions

**Minimum Qualifications**

+ Fosters collaboration, assigns tasks strategically, and motivates teams. Builds scalable structures and future‑ready capabilities.Leads teams through transformation and adaptstrategies proactively

+ Delivers strategic messages with clarity and confidence. Crafts compelling narratives to influence stakeholders. Leads complex discussions to achieve mutually beneficial outcomes

+ Applies deep knowledge of licensing models and audit methodologies. Drives innovation and transformation across compliance ecosystems. Aligns compliance with sales and customer success motions

+ Uses telemetry and audit data to inform decisions. Anticipates challenges and mitigates revenue risks.Interprets financial data to guide strategy and resource allocation

+ Account Executives and Customer Success Managers to align compliance actions with account strategy

+ Engage with legal, marketing, and operations to ensure consistent messaging and resolution planning.Coordinate with GTM Strategy & Operations to lead cross‑functional initiatives to embed compliance insights into broader go‑to‑market motions

+ Influence global teams to integrate compliance into strategic account planning and execution

+ Mentor junior team members and contribute to team development and knowledge sharing

**Learn More**

**About Autodesk**

Welcome to Autodesk! Amazing things are created every day with our software - from the greenest buildings and cleanest cars to the smartest factories and biggest hit movies. We help innovators turn their ideas into reality, transforming not only how things are made, but what can be made.

We take great pride in our culture here at Autodesk - it's at the core of everything we do. Our culture guides the way we work and treat each other, informs how we connect with customers and partners, and defines how we show up in the world.

When you're an Autodesker, you can do meaningful work that helps build a better world designed and made for all. Ready to shape the world and your future? Join us!

**Salary transparency**

Salary is one part of Autodesk's competitive compensation package. Offers are based on the candidate's experience and geographic location. In addition to base salaries, our compensation package may include annual cash bonuses, commissions for sales roles, stock grants, and a comprehensive benefits package.

**Belonging**

We take pride in cultivating a culture of belonging where everyone can thrive. Learn more here: Onboarding and Identity Verification

This role may require in-person onboarding and/or in-person ID verification.

**Are you an existing contractor or consultant with Autodesk?**

Pharmacovigilance Regulatory Reporting (Trilingual)

São Paulo, Brazil
Buenos Aires, Argentina
Full time
R
As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities.
Review, assess, and process safety data and information received from various sources. Distribute reports/data to internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members. This is a trilingual role requiring fluency in English, Spanish, and Portuguese.

Essential Functions

• Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
• Ensure compliance with quality, productivity, and delivery standards per project requirements.
• Track cases as applicable to the project plan.
• Identify and report quality problems to senior team members.
• Liaise with different functional team members and health care professionals to address project‑related issues.
• Attend project team meetings and provide feedback to the operations manager on challenges, issues, or successes.

Qualifications

• Bachelor's degree in life sciences
• Languages: Advanced level of English, Spanish and Portuguese.
• 1 year of experience in pharmacovigilance activities (mandatory) Specifically in regulatory reporting, will be highly valued.
• Previous experience working with Argus is desirable.
• Good knowledge of medical terminology and applicable safety databases.
• Strong organizational skills, attention to detail, and ability to work independently and as part of a team.

Work modality

100% home-based

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development