IQVIA Posted October 2, 2026

Qualitative Project Manager, Patient Centered Solutions

Mexico City, Mexico Full time
Quality Manager
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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

Overview

IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle.

The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into the development and commercialization of medication and other drug/non-drug interventions. We focus on understanding and meeting the needs of our clients – mostly life science/pharmaceutical companies – through the application of broad consulting expertise and technical scientific knowledge to design scientifically rigorous research. This research is broad and includes qualitative (e.g. interviews, focus groups), quantitative (e.g. clinical outcome assessments (COAs)/patient-reported outcomes (PROS), preference research) and passive (e.g. digital health technology tools) approaches to understand patient, caregiver and healthcare professional experiences and expectations of disease and treatment.

To meet our client expectations and retain the excellent reputation built up over time the IQVIA PCS team is committed to recruiting, training and supporting driven individuals who have both consulting skills and life science skills that can be applied to PCS research activities. Individuals joining us are assured of a rewarding and progressive career in patient-focused research. You’ll have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in developing and delivering solutions.  We operate in a truly multi-cultural, collegial, and collaborative work environment that is rich in development and growth.

Role Description

As part of the Study Execution Team (SET), the Qualitative Project Manager will be responsible for the execution of all operational aspects of the data collection phase of Patient Centered Solutions (PCS) studies which include a primary research phase.  The Qualitative Project Manager will be an integral member of study teams and will be involved in proactive project planning and take ownership of the management of study fielding.  The abilities to multi-task, “think fast on your feet”, creatively problem-solve, and provide accurate information, logistical solutions and support and quality results are keys to success.

The Qualitative Project Manager will:

As part of the project team, will manage and ‘own’ the primary research process from determining feasibility through study closeout.

Inform/develop recruitment and overall execution plan, determine feasibility, develop timelines and secure cost estimates with various recruitment partners and/or sites

Review recruitment materials for Institutional Review Board (IRB) submission

Provide input on relevant operational aspects of study protocol

Provide input on screening documents, confirmation of diagnosis (COD), recruitment outreach materials.

Provide input on quantitative survey materials

Manage recruitment process

Secure recruitment partners (vendors, patient advocacy groups (PAGs), sites) and ensure all logistical pieces are in place: required training, contracting and purchase orders, invoicing, sFTP sites, interviewing platforms, required programming of online materials

Laisse with other SET members to provide details related to and for actioning relevant project tasks.

Provide research materials, align with project team on recruitment processes, conduct project kick-off calls with vendors, ensure accuracy of recruitment tracker.

Monitor recruitment process to ensure all participants meet criteria and requirements are met, act as point person for all recruitment partners

Manage programming and launching of any online recruitment/interviewing materials

Provide regular internal/external recruitment/project updates

Work with vendors/sites to meet timing and quality standards

Ensure compliance with IQVIA requirements and SOPs

As needed:

Screen and schedule KOLS, patients, secure informed consent forms and CODs

Coordinate transcriptions

Coordinate payment of honoraria

Approve vendor invoicing

Create/request purchase orders

Facilitate contracting with PAGs, clinicians, vendors, subcontractors, etc.

Ensure new vendors/partners are set up within internal systems

Budget tracking: own financial tracking for out-of-pocket costs and billable time

Ensure all legal and fiduciary requirements are consistently met

Receipt of high-quality deliverables from partners

Safeguards against unnecessary expenses, inefficiencies, and poor delivery

Compliance with legal requirements (fair market value, anonymity, etc.)

MINIMUM EDUCATIONAL AND EXPERIENCE REQUIREMENTS:

Bachelor’s degree in Business Administrtion or related field.

5-7 years project management experience, preferably in market research, healthcare, or pharmaceuticals.

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.

Job details

Seniority
Manager
Function
Quality
Therapeutic area
Not listed
Location
Mexico City, Mexico
Employment type
Full time

How this role compares

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

We currently track 330 comparable Manager Quality roles across 82 biopharma companies.

330Comparable roles tracked
304Currently active
82Companies hiring similar roles
36Countries represented

Salary context

54 of 330 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
Lowest disclosed · Associate I, Quality Control, Raw Materials · ModernaTX, Inc. $53,500/yr – $85,600/yr
Highest disclosed · Advisor, Design Validation & Learning, Biotherapeutics · Lilly $168,000/yr – $268,400/yr
Peer group range $69,550 – $218,200 (median $166,200)

Where these roles are based

Top locations among the 330 comparable roles

United States138
India26
Ireland24
China24
Germany14
United Kingdom11

+ 30 more countries

Seniority mix

330 of 330 peers have a known seniority level

Manager216
Associate68
Associate Director46

Therapeutic area mix

0 of 330 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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
Novartis Insurgentes, Mexico Manager
Same function Same seniority Same country
60%similar
Johnson & Johnson Mexico City, Mexico Manager
Same function Same seniority Same country
45%similar
AbbVie North Chicago, IL Manager
Same function Same seniority
45%similar
Gilead Sciences, Inc. Foster City, United States Manager
Same function Same seniority
45%similar
McDermott Laboratories Limited Northern Cross, Ireland Manager
Same function Same seniority
45%similar
Mylan Teoranta Inverin, Ireland Manager
Same function Same seniority

Notify me about similar jobs

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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%
Senior eCompliance Manager
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Function Therapeutic area Seniority Country
45%
Senior Manager, Quality Assurance
Gilead Sciences, Inc. · Foster City, United States · Manager
Function Therapeutic area Seniority Country
45%
Qualified Person Manager (Határozott időre)
Mylan Hungary Kft. · Komárom, Hungary · Manager
Function Therapeutic area Seniority Country
45%
Senior Manager Quality Assurance, Drug Product (Filling)
Regeneron Pharmaceuticals, Inc (USA) · Renss, United States · Manager
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.