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Project Manager I EDS

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Join ICON plc, a global clinical research leader, as a Project Manager I EDS. This hybrid role in Whitesboro, NY requires 3+ years of lab or project management experience. You will manage bioanalytical project timelines, budgets, and client coordination. We offer competitive health insurance, ret...
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Location
United States , Whitesboro
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Salary
68616.00 - 85770.00 USD / Year
Expiration Date
Until further notice

Commercial Legal Counsel

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Join ICON as a Commercial Legal Counsel in Warsaw. Provide pragmatic legal advice and negotiate complex agreements for Pharma and Biotech clients. Leverage 2-5 years of in-house or law firm experience in commercial contracts. Enjoy competitive benefits including health insurance and a global supp...
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Location
Poland , Warsaw
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Salary
Not provided
Expiration Date
Until further notice

Clinical Site Associate (In-House CRA)

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Join ICON plc as an In-House CRA in Ankara. Utilize your life sciences degree and clinical research skills to support site management, document compliance, and data oversight. Enjoy a comprehensive benefits package while contributing to global clinical development in a collaborative, fast-paced e...
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Location
Turkey , Ankara
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Salary
Not provided
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Until further notice

Regulatory Technician

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Join our team in Mexico City as a Regulatory Technician. You will manage clinical trial submissions using the CTIS system, ensuring compliance and quality. Ideal candidates have advanced English and 1-2 years in clinical research. We offer competitive health insurance and retirement plans.
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Location
Mexico , Mexico City
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Not provided
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Until further notice

Senior Clinical Research Associate

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Join ICON plc as a Senior Clinical Research Associate in Taipei. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, r...
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Location
Taiwan , Taipei
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Salary
Not provided
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Until further notice

Clinical Site Associate

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Join ICON plc, a global clinical research leader, as a Clinical Site Associate in Reading, UK. Support trial operations by ensuring site compliance, documentation accuracy, and audit readiness. This role requires a life sciences degree, strong organizational skills, and offers competitive benefit...
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Location
United Kingdom , Reading
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Salary
Not provided
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Until further notice

Senior Manager, Clinical Supplies Management

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Lead global clinical trial material (CTM) operations from Warsaw. This senior role requires 8+ years in clinical supply planning, vendor management, and cGMP/GCP. You will oversee packaging, inventory, and logistics, providing strategic supply chain leadership. We offer competitive health insuran...
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Location
Poland , Warsaw
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Salary
Not provided
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Until further notice

Clinical Site Associate

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Join ICON plc as a Clinical Site Associate (In-House CRA) in Hong Kong. Support clinical trial operations, ensuring site compliance and documentation accuracy in this hybrid office role. Utilize your life sciences background and organizational skills within a world-leading CRO. Enjoy competitive ...
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Location
Hong Kong , Hong Kong
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Salary
Not provided
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Until further notice

Manager, Accounts Receivable

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Lead the Accounts Receivable function for a global clinical research leader in Chennai. You will manage a team, optimize collections, and minimize delinquencies using your 5+ years of AR expertise. We offer competitive benefits including health insurance and a supportive, innovative environment.
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Location
India , Chennai
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Salary
Not provided
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Until further notice

Pharmacovigilance Assistant

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Join our Pharmacovigilance team in Warsaw or Sofia as an Administrative Assistant. Play a vital role in global projects, ensuring compliance and patient safety through meticulous administrative support. A life sciences background is beneficial. We offer competitive benefits including health insur...
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Location
Poland; Bulgaria , Warsaw; Sofia
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Salary
Not provided
Expiration Date
Until further notice
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