Project Coordinator I (US Remote) in Madison, Wisconsin at MERIT CRO, Inc.
MERIT CRO, Inc.
Madison, Wisconsin, United States
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Job Description
MERIT CRO, Inc. is a global clinical trial endpoint expert specializing in multiple therapeutic areas. We’re committed to making a difference and are seeking talented people to join our team. Collaboration and customer focus are at the core of everything we do. We value diversity and are interested in people with drive, dedication, and creative problem-solving skills. We offer flexible schedules and remote opportunities.MERIT is seeking a full-time Project Coordinator to work Monday thru Friday from 5:00 AM ET to 1:00 PM ET under direct supervision, assists the Project Management Division with the coordination and conduct of project management activities, including the creation and distribution of study-related documents. Carries out management directives in a professional, efficient, and thorough manner. Primary functions include supporting the management of clinical trial data in the EXCELSIOR™ cloud application environment; performing data upload, and quality control functions; recording and distributing meeting minutes, maintenance of controlled documents including Master Project Files; and providing support functions for clinical sites, reading centers, and clients according to company and/or study-specific procedures and Good Clinical Practices (GCP).ESSENTIAL DUTIES AND RESPONSIBILITIES: (Other duties may be assigned.)Administrative Duties:
- Assist in the management of office tasks, including organization and coordination of controlled documentsAssist with all aspects of study management Assist in the development of the project and regulatory documents; includes proofreading of documentsAssist in the creation, duplication, and dissemination of documents.Assist with responses to quality review auditsMonitor own work to ensure quality and completeness
- Assist with all study activities from start-up through close outOrganize and prioritize work assignments to complete assignments and tasks on time, with quality, and has the ability to anticipate problem areas in advance.Apply creative approaches and ideas to solve problems maximizing the effective use of appropriate resources.Initiation of Master Project File and maintenance of project documentsGenerate and email eligibility notifications Attend project meetings internally and with the sponsor (via teleconference or face-to-face) throughout the projectCommunicate with Shipping and Receiving Department to confirm shipment and receipt of study-related materials at the designated address.
- Understand the EXCELSIOR™ product, protocol, and conduct of clinical trials in sufficient detail to be able to adequately discuss tasks with study team membersAssist with the review of EXCELSIOR™ study-specific configurationManage and review site surveys; update EXCELSIOR™ for site registrationAssist with providing guidance and training to sponsors, CROs, clinical sites, and graders on the use of EXCELSIOR™, including software functionality and technical supportImage check-in and quality controlIssue and review data query responses to ensure completeness and accuracy of response relative to other dataReview, categorize, and respond to customer support and complaint tickets in the helpdesk applicationPerform and document periodic review of inactive users in EXCELSIOR
- Comply fully with company policies and Standard Operating Procedures (SOPs)Other responsibilities may be assigned as required
- Practices and responds with commitment and sensitivity toward satisfying the needs of internal and external customers. Promotes quality and continuous improvement philosophy.
- Demonstrates a commitment to maintaining a safe, clean, and orderly work area. Promotes and follows safety regulations and actively contributes to work safely.
- 401k Retirement Health InsurancePaid Holiday Paid Long-Term Disability insurancePaid Life InsurancePaid Time Off
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Job Location
Madison, Wisconsin, United States
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