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IQVIA
IQVIA
Sponzor vizuma H1BProizvodnjaSvetovanjeTrženje
IQVIA združuje analitiko zdravstvenih podatkov, napredno tehnologijo in svetovanje, da bi organizacijam pomagala pri reševanju zapletenih izzivov na področju znanosti o življenju in zdravstva. Njena platforma Connected Intelligence povezuje podatke in umetno inteligenco za podporo kliničnim raziskavam, razvoju tehnologij in napredku novih terapij. Ekipe podjetja delujejo na področju analitike, svetovanja in zdravstvenih tehnologij ter ponujajo priložnosti, povezane z raziskavami, digitalnimi inovacijami in prizadevanji za izboljšanje izidov zdravljenja pacientov.
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Delovna mesta v podjetju

Clinical Research Associate, Sponsor Dedicated

Monitor clinical trial sites and support protocol compliance, patient recruitment, and study documentation for IQVIA. Coordinate with site staff and project teams to help trials meet quality standards and milestones.

USZdružene države AmerikeFLFloridaKSKansasNJNew JerseyNCSeverna KarolinaUTUtah
74.500 $ – 197.500 $ / leto
Na lokacijiPolni delovni časJuniorSrednja ravenDiploma ni potrebnaZahtevani Jezik: angleščinaKlinične raziskave
Google Cloud Platform

Opis

  • Monitor sites through selection, initiation, routine visits, and study close-out.
  • Assess site performance and compliance with protocols, GCP, ICH guidelines, and regulatory requirements.
  • Plan and track patient recruitment and retention with investigative sites.
  • Train site staff on study protocols and maintain regular communication.
  • Document and escalate quality or compliance issues and support their resolution.
  • Track regulatory submissions and approvals, enrollment, CRF completion, and data query resolution.
  • Keep Trial Master File and Investigator Site File records complete and accurate.
  • Prepare monitoring reports, follow-up letters, and other study documentation.
  • Work with project teams across functions to support study delivery and milestones.
  • Support study start-up, site budget tracking, financial management, and site payments as needed.

Zahteve

  • A bachelor’s degree in life sciences, healthcare, nursing, or a related field is preferred.
  • Relevant education and professional experience may be considered instead of a degree.
  • At least two years of independent on-site monitoring experience in pharmaceutical, biotechnology, or CRO settings.
  • Strong knowledge of clinical research processes and regulations, including GCP and ICH guidelines.
  • Industry experience and training in therapeutic areas and clinical trial protocols.
  • Proficiency with Microsoft Word, Excel, and PowerPoint, plus mobile and electronic data capture tools.
  • Clear verbal and written communication with investigators, site personnel, sponsors, and internal stakeholders.
  • Strong organization, problem-solving, and time-management skills.
  • Ability to manage multiple priorities in a fast-paced setting.
  • Ability to work independently and build collaborative relationships with colleagues, clients, and study teams.

Ugodnosti

  • Health and welfare benefits are available.
  • Incentive plans, bonuses, or other forms of compensation may be offered.

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