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Ukraine | 21147 | 27-Mar-2020Due to continued growth, we are looking for a Clinical Research Associates (Level II or Senior) to work for a global and prestigious pharmaceutical company. This is a full time permanent role. Office-based in Kiev. Previous experience in on-site monitoring is required.
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Beijing | 25118 |Supports project teams through contributions to product development strategies and the design, planning, execution, analysis, and reporting of clinical studies, with a view toward establishing the conditions essential for determining safety, efficacy, and marketability.
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US-Remote | 17946 | 29-Sep-2020Remote Senior Biostatistician with 5-7 years of Pharma or Biotech industry experience
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Poland | 24278 | 19-Nov-2020Exciting job opportunity in risk based monitoring. This is a global position, Sponsor dedicated.
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US - Remote | 24725 | 19-Oct-2020DOCS is currently seeking an experienced individual for a home-based Clinical Bioanalytics Operations Manager. This position requires previous experience in a pharma/CRO setting and experience working with bioanalytical data.
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Home Based in UK or Marlow / Eastleigh | 24514 | 08-Oct-2020At DOCS Global, an ICON Clinical Company, as part of long running global clinical & data operations FSP with a TOP 10 Pharma company, we are currently recruiting for an experienced Clinical Data Management Project Lead to join us in the UK.
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Warsaw, Poland | 24437 |Great job opportunity for experienced Line and Project Manager
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UK - Home-based | 24785 | 22-Oct-2020Are you interested in a full-time, permanent and home-based Clinical Pharmacology project management role with a multinational pharmaceutical company? Apply to DOCS!
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Stockholm, Sweden | 23810 |We are seeking a Clinical Program Leader based in Stockholm. In this role, you will lead and manage the cross-functional global Clinical Team, to ensure delivery of all clinical program activities to agreed timelines, budget and quality.
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Chile - Santiago | 24478 | 06-Oct-2020A Clinical assistant is responsible for set-up, tracking and maintenance of study activities (i.e regulatory documents, contracts and grants payments) including in- house management of documentation generated by the clinical sites. Responsible for the maintenance of the Local Study File (LSF)...