IQVIA Posted October 30, 2026

Director, MedTech Safety - Europe

Warsaw, Poland Full time
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IQVIA is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

IQVIA MedTech is seeking an experienced Safety leader to oversee a growing team responsible for safety activities supporting Medical Device clinical studies in Europe. This role will provide both technical and operational leadership, with primary responsibility for EU medical-device safety reporting, team management, client delivery, financial oversight, and the continued development of the Safety organization as the portfolio grows.

This leader will initially oversee and help build a team that is responsible for expedited and periodic safety reporting to European Ethics Committees and Competent Authorities, annual progress reporting.

Essential Functions

Medical Device Safety Leadership

Provide senior leadership and oversight for safety activities supporting Medical Device clinical studies, with a particular focus on studies conducted in Europe.

Ensure appropriate execution of expedited and periodic safety reporting to EU Ethics Committees and Competent Authorities.

Oversee preparation and delivery of annual and periodic safety/progress reports.

Serve as a senior Safety subject matter expert for clients, internal stakeholders, operational teams, and integrated partners.

Provide guidance on European Medical Device safety requirements and ensure operational processes meet applicable regulatory, contractual, quality, and reporting requirements.

Partner with US Safety team and cross-functional leaders to resolve complex operational, regulatory, and client issues.

Team Leadership

Lead, develop, and manage a team of Safety Specialists and Safety Managers.

Support the continued build-out of the Safety organization as additional positions are approved and client work expands.

Provide day-to-day leadership, coaching, workload oversight, performance management, and professional development.

Ensure appropriate staffing, resource allocation, utilization, training, and operational readiness across the team.

Establish clear accountability for quality, timelines, compliance, and client delivery.

Foster a collaborative, solutions-oriented culture focused on accountability, ownership, and continuous improvement.

Client and Program Leadership

Serve as a senior point of contact for assigned clients and programs, establishing strong and trusted client relationships.

Oversee scope, objectives, timelines, quality, and delivery for assigned Safety programs.

Ensure appropriate communication and escalation channels are maintained with clients and internal stakeholders.

Lead resolution of significant quality concerns, operational issues, and customer escalations.

Partner with customers to establish working practices, KPIs, SLAs, quality expectations, and processes for ongoing oversight.

Provide strategic consultation regarding Safety delivery and recommend solutions based on evolving client and program requirements.

Represent Safety in governance meetings, steering committees, operational reviews, and other high-visibility client forums.

Operational and Financial Management

Provide oversight of the financial and operational performance of assigned Safety work.

Manage and monitor revenue, billing, utilization, budgets, resourcing, and financial performance.

Ensure resources and staffing plans remain aligned with current and anticipated client demand.

Monitor program-level quality, productivity, utilization, and financial metrics and implement corrective actions when needed.

Support adherence to change-control processes and ensure changes in scope are appropriately assessed, documented, and reflected financially.

Partner with operational and commercial stakeholders as the team's responsibilities and book of business evolve.

Business and Strategic Leadership

Identify opportunities for repeat business and additional client services based on customer needs.

Participate in RFPs, proposals, solution development, budgeting, and customer presentations.

Provide Safety subject-matter expertise in the development of operational solutions for new opportunities.

Assess the operational feasibility, staffing requirements, regulatory considerations, and financial impact of proposed solutions.

Support development and negotiation of scopes of work, budgets, work orders, service-level agreements, and other applicable contractual documentation.

Lead or contribute to global initiatives designed to improve Safety delivery, processes, systems, oversight, and service offerings.

Collaborate across functions to develop practical solutions and ensure consistent delivery across programs and geographies.

Qualifications

Required

Bachelor's degree, preferably in a health science, life science, nursing, pharmacy, or related discipline, or an equivalent combination of education, training, and relevant experience.

At least 10 years of progressive Safety, clinical safety, or related experience within a CRO or Medical Device environment.

Demonstrated experience supporting Medical Device clinical studies.

Working knowledge and practical experience with European Medical Device safety requirements and EU safety reporting, including interactions or submissions involving Ethics Committees and Competent Authorities.

At least 3-5 years of leadership, people-management, or line-management experience.

Experience leading Safety professionals and managing priorities across multiple programs or studies.

Experience with client-facing delivery and senior stakeholder management.

Demonstrated understanding of operational and financial management, including revenue, billing, utilization, budgets, and resource planning.

Ability to manage competing priorities and make independent operational decisions in a complex, matrixed environment.

Strong written and verbal communication, presentation, negotiation, and client-management skills.

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 and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is zł310,300.00 - zł659,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Job details

Seniority
Director
Function
Pharmacovigilance
Therapeutic area
Not listed
Location
Warsaw, Poland
Employment type
Full time

How this role compares

Computed from every other active Pharmacovigilance role in our database, not just this employer's listings.

We currently track 38 comparable Director Pharmacovigilance roles across 21 biopharma companies.

38Comparable roles tracked
38Currently active
21Companies hiring similar roles
8Countries represented

Salary context

16 of 38 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Highest disclosed · Senior Director, US Risk Management & Product Safety (REMS) · Novartis $204,400/yr – $379,600/yr
Peer group range $208,800 – $292,000 (median $264,000)

Where these roles are based

Top locations among the 38 comparable roles

United States27
Denmark3
United Kingdom3
Morocco1
Poland1
India1

+ 2 more countries

Seniority mix

38 of 38 peers have a known seniority level

Director30
Senior Director5
Principal3

Therapeutic area mix

11 of 38 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Neuroscience4
Oncology3
Immunology2
Ophthalmology1
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
GSK Services Sp. z o.o. Warsaw, Poland Director
Same function Same seniority Same country
45%similar
AbbVie North Chicago, IL Director
Same function Same seniority
45%similar
Gilead Sciences, Inc. Foster City, United States Director
Same function Same seniority
45%similar
Otsuka Pharmaceutical Development and Commercialization, Inc. Princeton, United States Director
Same function Same seniority
45%similar
BioNTech Cambridge, Morocco Director
Same function Same seniority
45%similar
BioNTech Mainz, Germany Director
Same function Same seniority

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Pharmacovigilance job in Poland, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
SERM Medical Director / SERM Scientific Director
GSK Services Sp. z o.o. · Warsaw, Poland · Director
Function Therapeutic area Seniority Country
45%
Director, Product Lead, Clinical Safety & Pharmacovigilance (CSPV)
Otsuka Pharmaceutical Development and Commercialization, Inc. · Princeton, United States · Director
Function Therapeutic area Seniority Country
45%
Global Safety Physician / Safety Asset Leader Director
Ipsen Biopharm Ltd · London (UK), United Kingdom · Director
Function Therapeutic area Seniority Country
45%
Senior Medical Director - Patient Safety
AbbVie · Irvine, CA · Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.