This is an excellent opportunity to be a part of a growing team and work in a progressive environment, Please contact me at your earliest convenience.
Urgent requirement for one of our top clients located in “Branchburg, NJ”.
Please contact me at your earliest convenience, along with job No. SMW_92008 to xxxxxx.xxxxxx@xxxxxxxxx.xxx
Description:
Contribute to data management activities related to drug product development for assigned compounds or indications. Collaborate with internal biostatistics, Clinical Operations, and CRO data management and biostatistics. Collaborate with Biostatistics and Clinical Operations on database design, edit checks, data review and data extracts. Review data definition files and other DM or biostatistical components of a submission to ensure content meets Regulatory agency submission requirements. Review CRF for consistency with company standards
Requirements:
B.S. required. Preference in science or computers. Two years experience in clinical trials in a data management role. Experience with cancer clinical trials preferred Knowledge of FDA, EMEA and ICH guidelines and regulations covering clinical trials, statistics, and data management preferred and Knowledge of EDC and CDISC preferred.
Contact:
The most effective way of communication is via email please forward us your updated WORD FORMAT resume (Address, Contact number and email is must) to *** xxxxxx.xxxxxx@xxxxxxxxx.xxx ***
Please mention your best hourly rate, availability and visa status. Any questions, do feel free to email us.
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