Company DescriptionArtech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• Assist in the management of the day to day operations of clinical trials including coordination and oversight of all CRO/clinical site/vendor activities, liaison between Clinical Operations Manager and CRO, manage scopes of work/budgets/invoice payments.• Participate in development of protocol, case report form, CRF guidelines and other study documents.• Prepare and/or review regulatory documents (e.g. ICF), contracts, requests for proposal.• Ensure the training of CROs/investigators on protocol, regulatory, Client SOPs and data issues.• Reviews and approves monitoring reports and ensures tracking of ongoing site issues.• Minimum of college degree in a relevant discipline.Qualifications• Bachelors degree in relevant scientific discipline preferred.• 1-2 years experience in pharmaceutical industry.Additional InformationSneha ShrivastavaTechnical Recruiter (Clinical/Scientific)Artech Information Systems LLC360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: 973.967.3348 | Fax: 973.998.2599Connect with us on - LinkedIn | Facebook | TwitterSummaryType: ContractFunction: ResearchExperience level: Mid-Senior LevelIndustry: Pharmaceuticals
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