| Required Clinical Trial Manager in Ridgefield,CT(USC,GC,EAD) at Ridgefield, Connecticut, USA |
| Email: [email protected] |
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http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=554973&uid= From: Arun, KPG [email protected] Reply to: [email protected] Hi, Hope you are doing well, Please find the job description below and let me know your interest. Position: Clinical Trial Manager Location : Ridgefield,CT(Hybrid) Project : 12 Months Interview: Video Supply chain Operatiosn Clinical operations Pharma exp SAP exp Well organized Detailed Orientated They will be working in a trial team so they will need to be a team player and like people. Strong communication skills This is an entry level position with a degree and 5 years exp without Responsible for Managing and performing tasks along the Clinical Trial Supply Chain for Investigational Medicinal Products (IMPs) within legal and regulatory requirements. Study specific contact for all final release file preparation, review, modification, and KPI activities, function cost estimates, project time-line system creation / updates, bulk and comparator product order placement and tracking, deviation and CAPA processing, regulatory submission document processing, filing and archiving activities for trial close out, and providing enabling function information to other teams. Additional services provided include Product Complaint evaluation, classification, and notification, temperature excursion evaluation and processing. Experts for multiple computer systems such as Daisy, FoCUS, Idea, eProvisions, SQAM, and BLePs to complete tasks, provide information, and act as key users Ability to learn multiple computer systems. SAP software based computer systems experience. MS Office and MS Teams experience. SKYPE Meeting or Virtual Meeting software experience. GMP and Pharmaceutical Industry Regulations knowledge. Keywords: microsoft Connecticut http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=554973&uid= |
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| 08:21 PM 22-Aug-23 |