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Loyal Source Government Services is looking for a qualified Staff Development Registered Nurse to work with the Gallup IHS in New Mexico as a civilian contractor promoting and restoring patients? health.\n\nOur employees are our greatest asset! Benefits to working with Loyal Source include but are
Description
Job Description
CLINICAL TRIAL DISCLOSURE SPECIALIST
LAWRENCEVILLE, NJ
Project Description:
The Clinical Trial Disclosure Specialist will provide the operational support of Clinical Trial Data Sharing and Publication of Patient Lay Summaries. Key business partners are Clinical Developmen
Supports the logistical aspects of clinical trial conduct in compliance with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs).
Works closely with members of the Clinical Team, specifically in activities of study set-up, conduct and completion of clinical studies.
Assist
Interpret data with support from supervisor and contribute to technical reports.
Initiate workflows for protocol and report uploads/approvals in relevant electronic documentation systems.
Plan and execute formulation of screening stability experiments.
Details:
The pay range we're offering is
25 - 2
Staff Laboratory
New grads are welcome to apply! Are you a certified Medical Technologist and tired of your current role? Do you aspire to work in a commercial lab setting that will offer you the chance to combat cancer risk for as many people as possible? If so, this might be a perfect position fo
Job Description
Seeking a Clinical Research Coordinator II to work for a highly reputable research institute in the Bay Area. Team is dynamic and quickly growing!
DUTIES INCLUDE:
Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research
A clinical research firm is in need of a Telecommute Database Developer.Core Responsibilities Include: Creating electronic Case Report Forms according to finalized protocols for EDC studiesCreating data entry screens according to the approved annotated Case Report Form for paper studiesDesigning, bu
Job Description
We are partnering with a reputable and highly innovative research group in the Bay Area seeking a Senior Clinical Trial Manager/Project Manager. Seeking someone with CRO/Sponsor experience. This individual will be responsible for both clinical operations and personnel management. Pay
ResponsibilitiesManages study scope, quality, timelines, budget and risks with the internal functional leads, CRO and vendors to ensure that overall project objectives are met. Responsible for the development and management of clinical trial documents including (but not limited to) protocols, Case R
Processes, proofreads, verifies and manages various clinical regulatory documents, ensuring they are submission-ready for publishing with an appropriate level of accuracy and consistency.
Communicates regularly with colleagues and management regarding timelines and conflict to timelines for word
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