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IQVIA

Runs drug trials and sells health data to pharma

Qualitative Project Manager - Patient Centered Solutions

Project ManagementConfirmed live in the last 24 hours
Full-timeMexico City, CDMX, MexicoNo salary listedIn-person

About the Job

Requirements

  • Bachelor’s degree in Business Administration or a related field.
  • Five to seven years of project management experience, preferably in market research, healthcare, or pharmaceuticals.

Responsibilities

  • Manage and own the primary research process from feasibility through study closeout as part of the project team.
  • Inform or develop recruitment and overall execution plans, determine feasibility, develop timelines, and secure cost estimates with recruitment partners or sites.
  • Review recruitment materials for Institutional Review Board submission.
  • Provide input on operational aspects of study protocols, screening documents, confirmation of diagnosis documents, recruitment outreach materials, and quantitative survey materials.
  • Manage recruitment and secure recruitment partners, including vendors, patient advocacy groups, and sites; ensure required training, contracting, purchase orders, invoicing, secure file transfer sites, interviewing platforms, and online-material programming are in place.
  • Liaise with other Study Execution Team members to provide details and action relevant project tasks.
  • Provide research materials, align with the project team on recruitment processes, conduct project kick-off calls with vendors, and ensure recruitment trackers are accurate.
  • Monitor recruitment to confirm participants meet criteria and requirements, and serve as the point of contact for recruitment partners.
  • Manage programming and launch of online recruitment and interviewing materials.
  • Provide regular internal and external recruitment and project updates.
  • Work with vendors and sites to meet timing and quality standards.
  • Ensure compliance with IQVIA requirements and standard operating procedures.
  • As needed, screen and schedule key opinion leaders and patients, and secure informed consent forms and confirmation of diagnosis documents.
  • Coordinate transcription and payment of honoraria.
  • Approve vendor invoices and create or request purchase orders.
  • Facilitate contracting with patient advocacy groups, clinicians, vendors, subcontractors, and other partners.
  • Ensure new vendors and partners are set up within internal systems.
  • Track budgets and own financial tracking for out-of-pocket costs and billable time.
  • Ensure legal and fiduciary requirements are consistently met.
  • Ensure high-quality deliverables are received from partners.
  • Safeguard against unnecessary expenses, inefficiencies, and poor delivery.
  • Ensure compliance with legal requirements, including fair market value and anonymity.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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