Report this job

---

What is the problem? *

Incorrect company
Incorrect location
Job is expired
Job may be a scam
Other

Sr. Clinical Data Manager, MS. Deg. in Pharm. + Toxico., Stat. w/ 2 yrs. of exp.; Create &/or rev. clinical data mngt. docu., incl. but not limited to study prot., data mngt. plan, clin. data rev. plan, data tran. agreem., CRF Compl. Guide., & data issue logs, & ensure study active. are cond.; Create & rev. eCRF specif., Edit Check, Query logic, Dyn. logic, & UAT test scripts to ensure clin. data is colle. & rev.; Man. man. data listings, rev., metrics, issues, & gen. manu. Quer. in soft., incl. Medidata Classic Rave, RaveX, Oracle Inform, & IBM Clin., to ensure data ent. is clean.; Integ. oper. of clin. data mngt. w/ req. of Clin., Proj. mngr., Biostat., med., & Safety depart. Reg. proj. status & issues; Mon. Clin. data to ensure clin. trials are cond. as per ICH/GCP guidel.; Exp. in CDASH, CDISC, 21 CFR Part 11, and GCDMP; Must be willing to travel and/or relocate to work in various worksites throughout the US. No telecommuting. Send resume to Nexpro Technologies Inc, 114 Crockett Rd, King of Prussia, PA 19406.