Early Phase Opportunities at INC Research

Early Phase Opportunities at INC Research

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Summary: Coordinates or co-leads assigned clinical research projects in accordance to Protocols, Standard Operating Procedures (SOPs), and applicable regulations.Essential Functions:1. Clinical Research Project Plan and Preparationa) Review of assigned protocols and other protocol documentation (ICF, IB) for accuracy, feasibility, timing, and resources.b) Prepares and...

16004886 Requisition #

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Summary: Conducts quality control reviews of in-process study procedures and desk review of study documents to ensure accuracy, completeness, consistency of data, and adherence to study requirements, applicable Standard Operating Procedures (SOPs), and Good Clinical Practice (GCP). Essential Functions:1. Performs quality control review of in-process (live) clinical and...

17001182 Requisition #

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Please note that this is a 3 month contract.Summary: Supports the activities of the Clinical Trial Documentation Coordinators and Early Phase business unit. Responsible for clinical research administration and documentation support including the compilation, submission, management, and filing of clinical and regulatory documents to the Research Ethics Board and the...

17001056 Requisition #

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Summary: Ensures compliance with INC Research’s regulatory activities at the Early Phase Unit. Verifies activities performed by the functional and/or operational groups at the Early Phase unit are completed per regulatory, protocol and SOP requirements. Oversees the Early Phase unit’s QC processes.Essential Functions:1. Ensures overall compliance at the Early...

17001069 Requisition #

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Summary: Supports compliance activities associated with maintaining and enforcing volunteer compliance with protocol, Standard Operating Procedures (SOPs) and clinical code of conduct. Supports facility service requirements which include conducting patrols, initiating evacuation plans as required, maintaining and monitoring of restricted access areas. Trouble shoots and...

16004436 Requisition #

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Summary:Responsible for conducting and documenting the clinical tasks required in the management of trials. Ensures subject safety and compliance with study Protocol, SOPs, and Clinic Rules and Regulations.Essential Functions:1. Performs all relevant clinical skills and non-clinical functions during study conduct as qualification and training permits including, but not...

16006005 Requisition #

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Summary: Assists with the conduct of clinical trials through the collection of biological samples, performing venipuncture, electrocardiograms, vital signs, tube labeling, sample processing, and other related tasks in accordance with Protocol, Good Clinical Practice, Standard Operating Procedures (SOPs), and relevant regulatory guidelines.Essential Functions: Collects,...

15006848 Requisition #

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SummaryPromotes safety and implements Study Protocol, Working Practices, Standard Operating Practices, and Good Clinical Practices in the conduct of clinical trials. Promotes Nursing Standards in compliance with the College of Nurses and Regulated Health Professionals Act.Essential Functions:1. Practices all relevant clinical skills and non-clinical functions during study...

16005080 Requisition #

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SummaryPromotes safety and implements Study Protocol, Working Practices, Standard Operating Practices, and Good Clinical Practices in the conduct of clinical trials. Promotes Nursing Standards in compliance with the College of Nurses and Regulated Health Professionals Act.Essential Functions: Practices all relevant clinical skills and non-clinical functions during study...

15006812 Requisition #

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Summary:Promotes safety and implements Study Protocol, Working Practices, Standard Operating Practices, and Good Clinical Practices in the conduct of clinical trials.Essential Functions:1. Practices all relevant clinical skills and non-clinical functions during study conduct as qualification and training permits.2. Ensures study volunteers are efficiently monitored and...

16002769 Requisition #

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