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Junior Biostatistician

Senior Clinical Trial Associate - East Coast or Hybrid Office-Based in Waltham, MA

Global Clinical Trial Manager (US/Canada Remote)

Imaging Project Manager

ICON Strategic Solutions

Senior Clinical Research Associate

CRA II

CRA I

CRA I - Epidemiologic and Late phase

CTA Intern

Estagiária de farmácia

Assistente de Projetos de TI

Senior Project Manager

Senior Clinical Lead

Head of gastrointestinal trials team

Clinical Study Coordinator

Clinical Team Manager 2

Clinical Team Manager 1

In-house CRA II

Study Start Up Associate

Document Management Specialist

Coordinator Facilities & Admin

Head Cashier

Administrative Assistant

Clinical Operations Manager

Sr Project Management Specialist

Clinical Research Associate

Safety Surveillance Reviewer

Clinical Scientist II

Clinical Trial Assistant III

Clinical Research Associate II

Clinical Research Associate I

Clinical Research Associate- Site Management in Research Institute

Clinical Research Coordinator

Sr. Clinical Research Assistant

Clinical Research Assistant

Clinical Research Intern

Intern

Graduate Pharmacovigilance Associate

Assistente de farmacovigilância

Analista de laboratório - Pesquisa e desenvolvimento

Analista de laboratório II

Analista de laboratório l

Estagiária

Akamai

Cloudflare DNS

Mimecast

Microsoft Office 365

Amazon AWS

Brightcove

Senior Clinical Research Associate at Icon Plc on Behalf of BeiGene

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries.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 advances, in an effort to advance their path toward cures. To learn more, visit www.iqvia.com.

Senior QA Auditor/Quality Manager - Sponsor Dedicated

Associate Director, Program Management â Patient Support Services â Remote

Neuromuscular Medical Science Liaison - Southeast - 3069922

IQVIA

Outlook

Oracle Cloud

VueJS

Amazon SES

OneTrust

Senior Clinical Research Associate I

Clinical Research Coordinator III

Klinar CRO was established in January 2009 for the international trials conducted in Turkey.Klinar CRO and its team has a deep experience over the clinical trials of different phases and post marketing surveillance studies.KlinAR is one of the leading and experienced foundations for conduct, organization and improvement of clinical researches in Turkey. Currently, KlinAR CRO  which is a member of DIA, has become one of the first  certified CRO to be approved by the Ministry of Health in Turkey, working in compliance with the principles of "Guideline For Good Clinical Practices"​.In addition to the main office based in Ankara, depending on the project needs, KlinAR provides home based personnel in İstanbul and in İzmir.We provide; Regulatory Services (EC and RA (Ministry of Health) Submissions of the trials are performed and followed-up by KlinAR CRO), Clinical Trial Management (Monitoring and Project Management, Site Management Organization, Post-marketing Surveillance Studies), Medical Affairs (project manager of the study and the medical advisor of KlinAR CRO cooperate in the formation of the report ensuring that obtained data is correctly and fully reflected in the report), Data Management (Data Management Unit constructs the study database and performs statistical analysis defined in the protocol), Investigator Meeting Organization, CRF Design, Study Protocol Design, Training Organziation .Clinical Trials, Post Marketing Trials, Site Management Organization, Electronic Data Capture and Compassionate Use are being conducted by KlinAR CRO.Apart from the local and international sponsor companies, KlinAR's cooperation with Clinical Research Institutions which operate worldwide is in progress.

Eray Kuecuek

Senior Clinical Research Associate at Icon Plc on Behalf of BeiGene at ICON Strategic Solutions

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