Parsippany, New Jersey, United States · On-site
$35/hr–$42/hr
Clinical Research Coordinator (CRC) – Raleigh, NC Location: Raleigh, NC Work Setup: On-site Schedule: 30 hours per week (Part-Time) About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and cl…
Skills: Clinical Research Coordination, GCP Guidelines, Patient Recruitment, ECG Performance, Specimen Collection
Zaventem, Flanders, Belgium · On-site
Ben jij een enthousiaste relatiebouwer met een passie voor de farmaceutische sector? Wil je impact maken binnen een dynamische omgeving waar autonomie, ondernemerschap en resultaatgerichtheid centraal staan? Dan is deze …
Skills: Relationship Building, Pharmaceutical Promotion, Communication Skills, Result Orientation, Time Management
Cambridgeshire, England, United Kingdom · Hybrid
HYBRID Primary Care Key Account Manager – East of England Territory: Cambridge | Colchester | Ilford | Romford IQVIA is looking to recruit a Primary Care Key Account Manager who will play a pivotal role in improving pati…
Skills: Pharmaceutical Sales, Account Management, Stakeholder Engagement, Relationship Building, NHS Structures
Vienna, Austria · Remote Solely
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and…
Skills: Psychiatric Assessments, Rating Scales, Structured Clinical Interviews, Clinical Research, CNS Trials
Zaventem, Flanders, Belgium · On-site
Ben jij een ervaren farmaceutisch afgevaardigde die zowel commercieel als inhoudelijk sterk staat? Krijg je energie van het uitbouwen van duurzame klantenrelaties, het analyseren van marktpotentieel en het behalen van am…
Skills: Pharmaceutical Sales, Account Management, OTC Portfolio Management, Market Analysis, Relationship Building
Halle, Lower Saxony, Germany · Hybrid
Mitarbeiter (m/w/d) Fallmanagement Healthcare – hybrid, Homeoffice möglich Halle (Saale), Germany | Vollzeit | Hybrid | Gestalte mit uns die Gesundheitsversorgung von morgen. Die IVM plus GmbH entwickelt innovative Verso…
Skills: Case Management, Customer Service, Data Maintenance, Documentation, Communication
Kuala Lumpur, Kuala Lumpur, Malaysia · On-site
As an Associate Consultant at IQVIA, your problem-solving, analytical, critical thinking and leadership skills will be called upon from day one. You will be responsible for the delivery of consulting projects. An Associa…
Skills: Problem Solving, Analytical Thinking, Critical Thinking, Leadership, Market Research
Sofia, Sofia-City, Bulgaria · On-site
About the Role We are seeking an experienced and results-driven Project Manager to lead cross-functional initiatives and ensure successful project delivery. The ideal candidate will be responsible for planning, executing…
Skills: Project Planning, Stakeholder Management, Risk Mitigation, Budget Management, Agile
London, England, United Kingdom · Hybrid
Heart Failure Specialist Pharmacist and Independent Prescriber ATTR-CM Amyloidosis Support Programme Part-time – 3 days a week (remote with 1 day a week onsite in London) We are seeking an experienced Heart Failure Speci…
Skills: Independent Prescribing, Heart Failure Management, Clinical Pharmacy, Patient Education, Remote Clinical Consultations
Carlsbad, California, United States · Remote OK
$126k–$350k/yr
Location: Remote, must be based in US OVERVIEW Associate Principals are methodologic experts with substantial experience in providing consulting services to Pharmaceutical clients. Associate Principals are project leader…
Skills: Systematic Literature Review, Indirect Treatment Comparison, Network Meta-Analysis, Bayesian Statistical Analysis, Project Management
Buenos Aires, Argentina · On-site
Clinical Lead (Clinical Trial Management) - Global Study Leadership At IQVIA, our Clinical Leads play a vital role in bringing innovative medicines to patients worldwide. You'll provide clinical leadership across regiona…
Skills: Clinical Trial Management, Patient Recruitment, Site Performance Management, ICH-GCP Guidelines, Clinical Quality Oversight
Sofia, Sofia-City, Bulgaria · On-site
Job Overview Lead and manage the strategic, operational, and financial delivery of Site Activation activities across assigned studies and regions. This role is responsible for accelerating site activation to support time…
Skills: Site Activation, Project Management, Clinical Research, Regulatory Submissions, Stakeholder Management
Durham, North Carolina, United States · On-site
$88k–$220k/yr
At IQVIA, we are driven by our dedication to healthcare and our passion for technology. As a Product Manager you will harness the power of cutting-edge technology to create solutions that seamlessly unite patients with v…
Skills: Product Management, Roadmap Development, Stakeholder Management, Business Analysis, Project Management
Kaunas, Kaunas County, Lithuania · On-site
$45k–$55k/yr
IQVIA is recruiting Immunology & Inflammation Account Specialist in Lithuania to cover the Baltics on behalf of one of our pharmaceutical partners to support the promotion of a portfolio of specialty medicines within spe…
Skills: Pharmaceutical Sales, Customer Engagement, CRM Systems, Territory Management, Communication Skills
Buenos Aires, Argentina · Remote OK
The Site Enablement Lead (SEL) supports clinical study execution by identifying and enabling trained and qualified clinical research staff who are dedicated to a specific study or group of studies at a research site with…
Skills: Clinical Trial Conduct, Patient Recruitment, ICH/GCP Guidelines, Portuguese Fluency, Spanish Fluency
Bucharest, Romania · On-site
IQVIA is looking for a Recruiter based in the Romania to support hiring across Medical Sales and Medical Affairs functions within the pharmaceutical and life sciences industry. This is a delivery‑focused recruitment role…
Skills: End-to-end Recruitment, Candidate Sourcing, Candidate Screening, ATS Management, Pipeline Development
Livingston, Scotland, United Kingdom · On-site
Job Overview: As an Accountant 2 within IQVIA's EMEA General Accounting Team you will deliver high-impact accounting services across multiple EMEA entities ensuring timely accurate and fully compliant financial reporting…
Skills: General Ledger, Month-end Close, Balance Sheet Reconciliation, Journal Entries, Financial Reporting
Bogota, Capital District, RAP (Especial) Central, Colombia · On-site
Location: Bogotá, ColombiaJob Overview We are seeking an experienced Line Manager, Clinical Operations to lead and develop a team of clinical research professionals supporting the successful delivery of clinical studies.…
Skills: People Leadership, Clinical Monitoring, Resource Management, Stakeholder Management, Customer Relationship Management
Vienna, Austria · Remote OK
Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requiremen…
Skills: Site Activation, Regulatory Affairs, Clinical Research, GCP/ICH Guidelines, Project Planning
Warsaw, Masovian Voivodeship, Poland · On-site
$104k–$130k/yr
To support ongoing growth across Europe, IQVIA is hiring a Recruiter in Poland to support recruitment for Medical Sales and Medical Affairs roles within the life sciences sector. This role is suited to a recruiter who en…
Skills: End-to-end Recruitment, Sourcing, Candidate Engagement, LinkedIn Sourcing, Candidate Screening
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Coordinate and support clinical research studies by performing clinical procedures and managing participant recruitment and enrollment. Ensure data integrity through accurate entry into EDC systems and maintain audit-ready regulatory documentation.
Requires at least one year of clinical research experience and working knowledge of GCP guidelines and medical terminology. A bachelor's degree in health or life sciences is preferred along with experience in CRIO and regulatory filing.
Location: Raleigh, NC
Work Setup: On-site
Schedule: 30 hours per week (Part-Time)
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation. By combining deep scientific expertise with advanced technology, we help transform clinical research and bring new therapies to patients faster.
IQVIA is seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to support the successful execution of clinical research studies under the direction of the Principal Investigator. This role offers the opportunity to work directly with research participants, contribute to groundbreaking clinical trials, and ensure the highest standards of patient care, data quality, and regulatory compliance.
The ideal candidate has hands-on clinical research experience, is comfortable performing study-related procedures, and possesses strong organizational skills in both data management and regulatory documentation.
Key Responsibilities
Coordinate and support clinical research studies in accordance with study protocols, sponsor requirements, and Good Clinical Practice (GCP) guidelines.
Perform study-related clinical procedures, including ECGs, vital signs, specimen collection, and other protocol-required assessments.
Recruit, screen, enroll, and educate study participants while ensuring participant safety and retention.
Prepare study materials, maintain equipment, and coordinate study logistics to support efficient study conduct.
Accurately collect, review, and enter study data into Electronic Data Capture (EDC) systems.
Review source documentation and ensure timely resolution of data queries and discrepancies.
Support regulatory activities, including maintaining electronic study files and ensuring documentation is audit-ready.
Collaborate with investigators, sponsors, monitors, and study team members to ensure protocol compliance and data integrity.
Serve as a patient advocate while maintaining a safe and compliant research environment.
Minimum of 1 year of clinical research experience in a Clinical Research Coordinator or related role.
Working knowledge of clinical trial processes, GCP guidelines, and medical terminology.
Experience performing accurate clinical data entry and managing study documentation.
Familiarity with Electronic Data Capture (EDC) systems and data query resolution.
Strong organizational skills, attention to detail, and ability to manage multiple priorities in a fast-paced research environment.
Ability to build effective relationships with patients, investigators, sponsors, and study team members.
Bachelor's degree in a health science, life science, or related field, or an equivalent combination of education and relevant experience.
Experience utilizing CRIO (Clinical Research IO) to review and receive source data prior to EDC entry.
Experience supporting regulatory processes, including electronic regulatory filing, document maintenance, and ensuring study documentation complies with sponsor and regulatory requirements.
Experience with source document review, data reconciliation, and maintaining high standards of data quality and compliance.
Please note: This position is not eligible for employment sponsorship.
#LI-CES and #LI-DNP #LI-HCP #remote
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 proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
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 is $35.00-$42.00 per hour. 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.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
