The main responsibility of the Site Contract Leader is the negotiation of study specific, generic, site specific and country Clinical Site Agreements (CSA) and any other agreement that is required for the completion of the Site Initiation Visit (SIV). The Site Contract Leader is also responsible for managing CSA activities and liaising with study specific stakeholders to

Site Feasibility Liaison1 Sr.CRACRA II 1 Web CRO / 1

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The HR Associate acts as a first point of contact and support for managers and employees who require HR assistance with using or accessing HR programs and processes. The Associate is responsible for providing a timely and accurate response or properly redirecting the inquiry, to help the employee resolve or address their need. May serve as an SME or SPOC for a HR program,

The main focus of the role is to provide leadership and management to Project Quality & Risk Management staff.Identify, innovate and implement quality improvement opportunities at the project , client , operational , department or cross department level. Key Accountabilities Collaborate with senior leadership to develop and implement the strategy and direction for the PQR

Manage Projects & Technology Lead and implement the setup of Data Receipt Agreements with vendors by working with cross functional teams. Programming and setup of Import procedures to allow the ingestion of data either using SAS or alternative technology (e.g. "Workbench") Programming of reconciliation checks to ensure appropriate transfer of data. Programming of offline

The Senior Initiation Clinical Research Associate ( Sr iCRA ) specialises in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing and driving the strategy for the Pre SIV / start up tasks of the study. The Sr iCRA can also support protocol amendments if applicable. This role in

More about you On your first day we'll expect you to have Experience Experience in Statistics and its applications to clinical trials or observational studies, in industry or course work Prior experience with SAS or R programming desirable Education A Masters or Ph.D. level education in biostatistics, statistics, mathematics, or another relevant discipline (preferred) Ski

GCP(Good Clinical Practice) SOP(Standard Operating Procedure) SDV Source Data Verification) CRF Case Report Form) IRB (Institutional Review Board) Job Qualifications CRA 1 Web Web