Amsterdam, North Holland, Netherlands · On-site
IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment. The sector we are in is cutting edge for thera…
Skills: Clinical Monitoring, GCP/ICH Guidelines, Site Evaluation, Source Data Verification, Clinical Trial Management
Buenos Aires, Argentina · On-site
Job Overview Site Enrollment and Engagement Lead - Argentina collaborate with research staff and key stakeholders to enhance trial recruitment and support study‑specific training needs. Serves as a strategic partner to i…
Skills: Patient Recruitment, Relationship Management, Clinical Trial Coordination, Stakeholder Management, Patient Retention
Parsippany, New Jersey, United States · Hybrid
$71k–$239k/yr
To be eligible for this position, you must reside in the same country where the job is located. This role is hybrid and will require going into an IQVIA office several times weekly in PA, NY, NJ or CT. Consultant - Comme…
Skills: Data Analytics, Business Consulting, Project Management, Pharmaceutical Commercial Business, Healthcare Data Analysis
Parsippany, New Jersey, United States · On-site
$80k–$85k/yr
Key Account Representative In partnership with our client, we are actively searching for Key Account Representatives to deliver on our commitment to serve patients. The Key Account Representative will be responsible for …
Skills: B2B Sales, Pharmaceutical Sales, Medical Device Sales, Negotiation, Persuasion
Paris, Ile-de-France, France · On-site
Créée en 2010, l’agence RCA Factory accompagne les acteurs de la santé dans la définition et la mise en œuvre de leur stratégie de communication social media et de marketing digital. RCA Factory propose une large gamme d…
Skills: Creative Direction, Generative AI, Team Management, Art Direction, Social Media Strategy
Sofia, Sofia-City, Bulgaria · On-site
Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health a…
Skills: Strategic Pricing, Pricing Models, Competitive Analysis, Excel, Budgeting
Beijing, Beijing, China · On-site
single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to prov…
Skills: Data Management, Project Planning, Clinical Data Management, Data Cleaning, Stakeholder Communication
San Francisco, California, United States · Hybrid
$60k–$274k/yr
Location: Hybrid (Boston, New York, or San Francisco)-50% in office Eligibility: Candidates must reside in the same country where the role is located Team Overview IQVIA Advisory Services is a cornerstone of IQVIA, deliv…
Skills: Management Consulting, Strategic Planning, Project Management, Pharmaceutical Industry Knowledge, Healthcare Industry Knowledge
Bratislava, Region of Bratislava, Slovakia · On-site
Job Overview Provides support to CMS leads on activities related to the CMS team, in partnership with project and clinical lead, and in collaboration with other functional teams, to achieve the delivery of the project’s …
Skills: Centralized Monitoring, Clinical Trial Management, ICH GCP, Risk Assessment, Data Integrity
Carlsbad, California, United States · On-site
The Part Time Clinical Consultant (PTCC) role is an exciting opportunity to join IQVIA. IQVIA/MedTech takes the approach to helping customers drive healthcare forward in this challenging, fast-paced environment. We help …
Skills: Ventricular Medical Device Support, Patient Management, Clinical Education, Case Support, Cardiac ICU Care
Carlisle, England, United Kingdom · On-site
Territory Business Manager Location: North Yorkshire, North East, North Cumbria Do you want to join a company that nurtures its employees and advocates for an employee work-life balance? Do you have excellent sales exper…
Skills: NHS Sales, Relationship Building, KPI Management, Analytical Skills, Dermatology Product Sales
New Providence, New Jersey, United States · On-site
$114k–$319k/yr
IQVIA Digital powers exceptional brand experiences, delivering innovative solutions based on a customer-first, insights-driven, and integrated omnichannel vision. We provide authenticated, privacy-enhanced data and analy…
Skills: Product Management, AdTech, MarTech, Media Measurement, Data Architecture
Madrid, Community of Madrid, Spain · On-site
We are looking for a Customer Success Manager to join the Research Practice in the Payers, Providers and Governments group, supporting the growth and adoption of innovative solutions that advance clinical and health rese…
Skills: Customer Success Management, Project Management, Service Delivery, Stakeholder Management, Client Networking
Durham, North Carolina, United States · On-site
$63k–$157k/yr
IQVIA Biotech is seeking Sr. Site Contracts Associate or Site Contracts Associate with 3-5 years' experience negotiating clinical site contracts and budget templates. This role requires candidates who have sponsor facing…
Skills: Clinical Site Contracting, Contract Negotiation, Budget Template Development, GCP/ICH Guidelines, Technical Writing
Wayne, Pennsylvania, United States · On-site
$54k–$136k/yr
Job Overview Provides the client relationship to a mid-sized client or clients through relationships with executives and leaders in the client organization in a part of mid-sized market or part of a large region. Grows r…
Skills: Account Management, Revenue Growth, Sales Presentations, Contract Expansion, Client Relationship Management
Carlsbad, California, United States · On-site
$72k–$189k/yr
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor r…
Skills: Site Monitoring, GCP, ICH Guidelines, Subject Recruitment, TMF Management
Carlsbad, California, United States · On-site
$72k–$189k/yr
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor r…
Skills: Site Monitoring, GCP, ICH Guidelines, Subject Recruitment, Trial Master File (TMF)
Dublin, Leinster, Ireland · On-site
Sales Account Manager Location: Ireland IQVIA is recruiting for a Medical Device Sales Specialist. In this role you will be responsible for developing sales in strategic accounts across London. You will become an integra…
Skills: Medical Device Sales, Account Management, Business Planning, Stakeholder Management, Value Proposition Presentation
Zaventem, Flanders, Belgium · Hybrid
For one of its customers IQVIA is looking to recruit a GP Engagement & Omnichannel Key Accountmanager (Women’s Health). This national function combines field and office-based work and and plays a key part in strengthenin…
Skills: Omnichannel Engagement, Business Development, Key Account Management, Digital Marketing, GP Relationship Management
Paris, Ile-de-France, France · On-site
Are you looking for an opportunity as a Clinical Research Nurse? Do you want to work for an industry leading company. This part-time role is to support a clinical trial in Marseille where you will need to visit patients …
Skills: Clinical Research, Patient Care, Medical Device Assistance, Clinical Trial Knowledge, Medical Terminology
Amsterdam, North Holland, Netherlands • On-site
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The role involves overseeing Phase I-IV clinical trials through site evaluation, initiation, and close-out visits. The CRA ensures compliance with Good Clinical Practices and manages communication between the sponsor and investigators.
Candidates must have 1-2 years of onsite monitoring experience and strong knowledge of GCP/ICH guidelines. Proficiency in both Dutch and English is required, along with the ability to work independently in a matrix environment.
IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment. The sector we are in is cutting edge for therapies with un-met medical need.
IQVIA Biotech has an exciting position within its EU Clinical Monitoring team. The Clinical Monitoring department is the largest team within IQVIA Biotech, providing CRA, Clinical Leads, Management and oversight to global clinical studies.
Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA to ensure all monitoring activities are conducted according to study requirements.
Participates in the investigator recruitment process, performing site evaluation visits of potential investigators to evaluate the capability of the site to successfully manage and conduct the clinical study.
Coordinate activities with the site and internal departments in preparation for the initiation of the study. Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF and EDC system; monitoring activities and study close-out activities.
Assists in resolving any issues to ensure compliance with site file audits in conjunction with ISS.
Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs.
Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory.
Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification and works with sites to resolve data queries and produce robust data.
May review protocols, eCRFs, study manuals and other related documents, as requested by the Clinical Trial Manager and/or Lead CRA.
Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.
Assists with, and attends, Investigator Meetings for assigned studies.
Attends study-related, company, departmental, and external meetings, as required.
Ensures all study deliverables are completed per IQVIA Biotech and study timelines
Conducts Field Evaluation Visits and field training of CRA Is, IIs and other Sr. CRAs.
Serves as mentor for junior CRAs and those new to the company and/or study.
Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology.
Minimum of 1-2 years of onsite monitoring experience is a must.
Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.
Able to form productive professional relationships both internally within own function, cross-functionally and externally with health care professionals.
Able to handle several priorities within multiple, complex trials.
Able to reason independently and recommend specific solutions in clinical settings.
Able to work independently, prioritize, and work within a matrix team environment.
Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research.
Candidates must have strong communication levels of Dutch and English.
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.
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Offices: 2400 Ellis Rd, Durham, North Carolina 27703, US
