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Trouvez des postes près de chez vous, sur site, hybrides ou à distance.- Emplois similaires à : Senior Clinical Research Associate
Clinical Research Associate II/Senior Clinical Research Associate
ICONNew YorkClinical Research Associate II/Senior Clinical Research Associate- Poznan ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and tre
Clinical Research Associate II or Senior Clinical Research Associate
ICONNew YorkClinical Research Associate II or Senior (FSP - Sponsor Dedicated) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments
Clinical Research Associate
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Clinical Research Associate I
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Biolinq IncorporatedSan DiegoJob Type Full-time Description WARNING about fake job posting scams. There has been a recent wave of scams whereby third parties post fake job openings using a bogus email address that resembles xxxx@
Clinical Research Associate II
AbbVieOrlandoCompany Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. W
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Clinical Research Associate (CRA) - Dallas
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IQVIA HoldingsDurhamSite Monitoring Manager To be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting
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Clinical Research Associate - Ohio/Michigan
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Clinical Research Associate - New York / New Jersey
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Clinical Research Associate II - Oncology - United States (Remote)
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Clinical Research Associate II/Senior Clinical Research Associate
- New York, New York, United States
- New York, New York, United States
À propos
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports
Your Profile: You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience:
Bachelor's degree in a scientific or healthcare-related field. Minimum of 1 year of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Willingness to travel as required
Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:
Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Compétences linguistiques
- English
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