Was emailed by this recruiter yesterday too--6-Month Clinical Trial Associate position: Greetings, My name is Md Perwaiz and I am recruiter at eTeam Inc. eTeam Inc is a global contingency staffing firm servicing fortune 1000 clients globally.We have an excellent job opportunity with one of our client. Job Title: Clinical Trial Associate Location: East Hanover,NJ Duration:6 months Job Description: Duties: Assist in the operational and logistical aspects of clinical trials according to ICH-GCP and internal Client procedures. Assist in delegated tasks to support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study. Provide support to the Clinical Trial Leader (CTL) with many of the tasks involved with the smooth running of clinical trials in compliance with Client processes. Collaborate with the CTL in taking action to address issues as they arise. Help manage clinical, regulatory and study-related essential documents such as study protocols, Case Report Forms, Informed Consent Forms etc.; review documents for completeness, accuracy and compliance with protocol and appropriate regulations. Identify issues and take appropriate corrective action as necessary. Interactions with Investigator sites e.g. to collect relevant documentation, provision of study materials / documents. Liaise with contract organisations, vendors and other suppliers of project support services to ensure study deliverables are met e.g. contribute to documentation, processes and set-up activities to facilitate efficient working and effective partnerships with external groups. Provide input on agendas, create materials, liaise with meeting planners and coordinate logistics for key meetings e.g. internal CTL meetings or external investigator meetings. May attend and present at these meetings as appropriate. Help ensure accuracy of clinical trial management databases and resource/budget tracking tools, providing information, maintaining meeting minutes and following up on questions as necessary. Help check for discrepancies and take actions to correct as necessary. Identify areas for process or technology improvements with regard to tasks undertaken within the role. Assist in the ordering of clinical trial supplies Assist in the compilation of the clinical study report and its appendices. Responsible for setting up and maintaining Trial Master Files and ensuring all relevant study documents are filed and archived based on the appropriate guidelines. Audit existing Paper Trial Master Files, collect outstanding documents and archive after study is completed. Assist the CTL in organizing Investigator/Site Initiation Meetings and/or First Dose/Monitoring Visits. Attend at least 1 of these meetings and assist the CTL in conducting. Maintenance of knowledge and training of ICH-GCP, current regulations and procedures. Skills: Fluent oral and written English Previous experience in clinical trials (e.g. clinical trial design, execution and operations) is preferred but not required Good organizational and interpersonal skills. Ability to work in a team as well as independently if required and to manage multiple priorities with support. Computer literate. Education: A bachelor¿s degree or equivalent qualification or work experience in life sciences or nursing. If you are qualified, available, interested, planning to make a change, or know of a friend who might have the required qualifications and interest, please call me ASAP at (732) 248-1900 Ext.412 even if we have spoken recently about a different position. If you do respond via e-mail please include a daytime phone number so I can reach you. Also, please take a few minutes to answer some of the questions below as they will help me qualify your candidature Full Legal Name as in Driving License/ Passport: Preferred email ID: Day/ Evening phone numbers: Current Location: Work Authorization: Earliest availability for Phone/ On-Site interview: Hourly Rate: Earliest possible start date: Two Professional References: Also, be aware that our client conducts an extensive background checks on candidates who are extended offers of employment. Sincerely yours, Regards, Md Perwaiz Alam malam@eteaminc || eteaminc
Posted on: Fri, 01 Nov 2013 09:56:01 +0000
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