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iconplc - United States, Raleigh

26 Job Offers

Job Offers

Site Management Associate I

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Join ICON as a Site Management Associate I in Raleigh or Blue Bell, US. Support non-client sponsored studies, including Investigator Sponsored Studies, with a focus on operational execution and document tracking. Ideal for candidates with a scientific degree and clinical research experience. Enjo...
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Location
United States , Raleigh, Blue Bell
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Not provided
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Manager, Clinical Operations

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Lead global clinical trials as Manager, Clinical Operations at ICON plc in Raleigh, Charlotte, or Blue Bell, US. Leverage 5+ years of CRO/pharma experience and strong GCP knowledge to drive Phase 1-4 study strategies. Manage vendor relationships, budgets, and cross-functional teams with limited s...
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Location
United States , Raleigh; Charlotte; Blue Bell
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Not provided
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Oncology Scientific Lead, Med Com (Associate Scientific Dir)

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ICON plc seeks an Oncology Scientific Lead (Associate Scientific Director) for its Global Medical Communications team. This hybrid role requires an advanced degree (PhD, PharmD, or MD) and 4-5 years of high-level content development in a medical communications agency. You will oversee scientific ...
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Location
United States , Raleigh; Texas; Tennessee; Blue Bell; Boston
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Not provided
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Clinical Outcomes Assessment Training Lead

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ICON seeks a Clinical Outcomes Assessment Training Lead in Raleigh, NC. You will design and deliver COA training for clinical studies, requiring a Master’s degree and extensive outcomes research experience. Key skills include advanced PowerPoint, video editing, and strong presentation abilities. ...
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Location
United States , Raleigh
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Not provided
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Senior Manager, Regulatory Affairs (Ad Promo)

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Senior Manager, Regulatory Strategy role in Raleigh, US. Leverage 7+ years of regulatory expertise to design clinical trials, develop submission plans, and advise ICON clients. Requires a Bachelor's in science/healthcare, supervisory experience, and strong strategic drug development skills. Benef...
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Location
United States , Raleigh
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Not provided
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Country Lead Monitor

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ICON plc seeks a Country Lead Monitor in Raleigh, NC, to drive clinical trial operations. You will manage study deliverables, ensure regulatory compliance, and build stakeholder relationships. Requires a science degree, therapeutic expertise, and prior monitoring experience. Enjoy competitive ben...
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Location
United States , Raleigh
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Not provided
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Talent Acquisition Business Partner

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ICON plc seeks a strategic Talent Acquisition Business Partner in Raleigh or Blue Bell, PA. You will drive full-cycle recruitment for healthcare and clinical research roles, leveraging data insights and ATS proficiency. This role demands strong stakeholder collaboration and a commitment to DEI. E...
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Location
United States , Raleigh; Blue Bell
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Not provided
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Talent Sourcing Recruiter

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Join ICON plc as a Talent Sourcing Recruiter in Raleigh, NC. Proactively build talent pipelines and engage passive candidates for critical roles across the USA and Canada. Requires sourcing expertise, ATS proficiency, and a hybrid schedule (3 days onsite). Ideal for recruiters with clinical resea...
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Location
United States , Raleigh
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Not provided
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Talent Acquisition Business Partner

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ICON seeks a strategic **Talent Acquisition Business Partner** in Raleigh or Blue Bell, PA. You will drive end-to-end recruitment, leveraging data insights and ATS proficiency to attract top talent in the healthcare and clinical research sectors. This role demands strong collaboration with hiring...
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Location
United States , RALEIGH, BLUE BELL
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Senior Clinical Research Associate

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Senior Clinical Research Associate opportunity in Raleigh, NC with ICON Plc. Manage and monitor clinical trial sites, ensuring GCP and regulatory compliance. Requires a Bachelor's in a scientific field, extensive CRA experience, and strong site management skills. Benefit from competitive health i...
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Location
United States , Raleigh
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Not provided
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Supplier Performance Monitor

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ICON plc seeks a Supplier Performance Monitor in Raleigh, NC, to oversee data quality and compliance for clinical trials. Ideal candidates possess laboratory auditing experience, with in-vitro diagnostics preferred, and relevant degrees plus 3-12 years of experience. This role involves monitoring...
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Location
United States , Raleigh
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Not provided
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Sr. Etrif Specialist

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Join ICON as a Sr. TMF Specialist in Raleigh, NC, and ensure clinical trial document accuracy. Leverage 2+ years of TMF experience and a life sciences degree to manage document integrity, conduct audits, and support cross-functional teams. Enjoy benefits like health insurance, retirement planning...
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Location
United States , Raleigh
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