IQVIA

Job OverviewProvide Trial Master File (TMF) - Quality checks related assistance to study teams.Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs) policies practices good clinical practices applicable regulatory requirements and meets quality and timel

Job OverviewProvide Trial Master File (TMF) - Quality checks related assistance to study teams.Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs) policies practices good clinical practices applicable regulatory requirements and meets quality and timel

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordina

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly If so come and join us - IQVIA are looking Clinical Research Coordina

The DTP Team Lead is responsible for leading a team of Content Design Specialists who ensure translation projects are delivered according to IQVIAs standards and design requirements. He/she builds and maintains strong relationships within his/her team with Project Managers as well as

The DTP Team Lead is responsible for leading a team of Content Design Specialists who ensure translation projects are delivered according to IQVIAs standards and design requirements. He/she builds and maintains strong relationships within his/her team with Project Managers as well as

The Content Design Specialist must check content in various languages to ensure it does not contain any design error. He/she must track omission inaccuracy inconsistency and visibility errors coming from OCR translation and DTP tasks. It may entail correcting removing adding and forma

The Content Design Specialist must check content in various languages to ensure it does not contain any design error. He/she must track omission inaccuracy inconsistency and visibility errors coming from OCR translation and DTP tasks. It may entail correcting removing adding and forma

We are seeking aresilient strategic and self-driven Key Account Manager(m/f/d) in Germany to further expand our footprint in theCardioplegia marketthrough aclient-dedicated role. You will be responsible for driving the customer journey experience in hospitals that undergo open-heart s

We are seeking aresilient strategic and self-driven Key Account Manager(m/f/d) in Germany to further expand our footprint in theCardioplegia marketthrough aclient-dedicated role. You will be responsible for driving the customer journey experience in hospitals that undergo open-heart s

The IQVIA Sponsor-Dedicated Clinical Trials Assistant Team issupporting the project teams in the execution of clinical the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved i

The IQVIA Sponsor-Dedicated Clinical Trials Assistant Team issupporting the project teams in the execution of clinical the team provides the opportunity to work with the preparation and documentation of clinical research projects in different therapeutic areas. You will be involved i

Job OverviewReview assess and process safety data and information across service lines received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under

Job OverviewReview assess and process safety data and information across service lines received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations Standard Operating Procedures (SOPs) and internal guidelines under

Project Role: Programmer Analyst or Software Devl Analyst 2Work Experience: 2 to 8 yearsWork Mode: HybridMust Have Skills: Veeva CDMS or Veeva CDBJob Roles & Responsibilities:Veeva CDMS -Veeva Vault CDMS knowledge: Deep understanding of Vault EDC Vault Coder and Vault DataWorkbench.CD

Project Role: Programmer Analyst or Software Devl Analyst 2Work Experience: 2 to 8 yearsWork Mode: HybridMust Have Skills: Veeva CDMS or Veeva CDBJob Roles & Responsibilities:Veeva CDMS -Veeva Vault CDMS knowledge: Deep understanding of Vault EDC Vault Coder and Vault DataWorkbench.CD

Job OverviewUnder direct supervision assist with the development and preparation of pharmacovigilance agreements for assigned customers.Essential Functions Under direct supervision work closely with project team to determine appropriate terms and conditions of safety agreements. Under

Job OverviewUnder direct supervision assist with the development and preparation of pharmacovigilance agreements for assigned customers.Essential Functions Under direct supervision work closely with project team to determine appropriate terms and conditions of safety agreements. Under

Senior Site Activation Coordinator ICF (Informed Consent Form)Locations: Bulgaria South Africa Slovakia SerbiaWork Model: HybridMake an impact on patient health with IQVIA!Join our Global Site Activation Team a 2000strong network driving highquality site activation and ensuring pa

Senior Site Activation Coordinator ICF (Informed Consent Form)Locations: Bulgaria South Africa Slovakia SerbiaWork Model: HybridMake an impact on patient health with IQVIA!Join our Global Site Activation Team a 2000strong network driving highquality site activation and ensuring pa

IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client envir

IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client envir

Location: Guatemala City Work Type: HybridAbout the RoleJoin our team as a Business Intelligence Analyst where you will be responsible for data investigation query resolution data transformations and delivering valuable insights to the business. This role supports internal stakeholder

Location: Guatemala City Work Type: HybridAbout the RoleJoin our team as a Business Intelligence Analyst where you will be responsible for data investigation query resolution data transformations and delivering valuable insights to the business. This role supports internal stakeholder

Job OverviewClinical Trial Manager are an integral part of clinical trial delivery working alongside clinical teams to improve patients lives by bringing new drugs to the market faster. The Clinical Trial manager is a member of the core project team responsible for the clinical delive

Job OverviewClinical Trial Manager are an integral part of clinical trial delivery working alongside clinical teams to improve patients lives by bringing new drugs to the market faster. The Clinical Trial manager is a member of the core project team responsible for the clinical delive

IQVIA Biotech is hiring an Associate Clinical Project Manager in Argentina.Job OverviewAssociate Project Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Associate Project Lead

IQVIA Biotech is hiring an Associate Clinical Project Manager in Argentina.Job OverviewAssociate Project Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Associate Project Lead

Job OverviewThe Clinical Lead provides leadership of the clinical team in support of the project leader and in collaboration with the other functional teams to achieve the delivery of the projects overall objectives to the Sponsors satisfaction per contract while optimizing speed qual

Job OverviewThe Clinical Lead provides leadership of the clinical team in support of the project leader and in collaboration with the other functional teams to achieve the delivery of the projects overall objectives to the Sponsors satisfaction per contract while optimizing speed qual

The Operational Effectiveness Specialist 2 is responsible for administering and optimizing proposal development technologies across Commercial Business Optimization & Technology (CBOT) and Research & Development Solutions (R&DS). This role manages user access maintains and updates sta

The Operational Effectiveness Specialist 2 is responsible for administering and optimizing proposal development technologies across Commercial Business Optimization & Technology (CBOT) and Research & Development Solutions (R&DS). This role manages user access maintains and updates sta

IQVIA is expanding its team and is seeking a Retail & Market Access Manager based inFrance. This is one of several newly created roles across the EU due to our customers ongoing success and ahead of product launches in 2026.Our customer is a global biopharmaceutical company dedicated

IQVIA is expanding its team and is seeking a Retail & Market Access Manager based inFrance. This is one of several newly created roles across the EU due to our customers ongoing success and ahead of product launches in 2026.Our customer is a global biopharmaceutical company dedicated

Clinical Research Coordinator Toledo (Part-Time 20-24hours/week)Start Date: immediatelyDuration: until 30th of September 2026IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Toledo. This part-time position offers a unique

Clinical Research Coordinator Toledo (Part-Time 20-24hours/week)Start Date: immediatelyDuration: until 30th of September 2026IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Toledo. This part-time position offers a unique

Our MedTech Healthcare Collection Associate will be responsible for collecting reprocessed medical equipment in a hospital. You will be working with surgical non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Processing Departments. Th

Our MedTech Healthcare Collection Associate will be responsible for collecting reprocessed medical equipment in a hospital. You will be working with surgical non-invasive and vascular equipment within areas of the hospital such as Operating Rooms and Sterile Processing Departments. Th

Clinical Research Coordinator Sioux Falls SDWork Setup: On-siteSchedule: Part-time (24 hours per week)Shape the Future of Medicine with IQVIA!Are you passionate about advancing healthcare and improving patient outcomes Join IQVIA as a Clinical Research Coordinator (CRC) and play a vi

Clinical Research Coordinator Sioux Falls SDWork Setup: On-siteSchedule: Part-time (24 hours per week)Shape the Future of Medicine with IQVIA!Are you passionate about advancing healthcare and improving patient outcomes Join IQVIA as a Clinical Research Coordinator (CRC) and play a vi