Sr. Clinical Data Manager, MS. Deg. in CIS., CS. w/ 6 mon.of exp.; Create clin. (DMP) & main. DMP though proj. life. Accor. to study des. & req.; Dev. Valid. Plans, Risk Assess., Trac.Matrix compl. to 21 CFR Part 11, Gxp, Data Int. std. & Audit Trails; Lead dev. of study spec. Data mngt. Plans, Vendor mngt. plans, Cross-func. data rev. plans, eCRF comp. guide., Data Trans.Spec., eTMF maps, & CDM doc.; Prep. SOPs, Data mngt. Plan, Coor. Data. Des., devel., impl., maint. & user supp. of clin.syst.; perf. & manage proj. close-out tasks incl. database lock / freeze, unbl. &, access changes; Supp. Data Managers thr. Subj. data rev., data listings, ident. data discr., verify data query resol. Include. Res.of data issues from clin. & stat.groups. Must be willing to travel and/or relocate to work in unanticipated locations throughout the US. Send Resume to PVR Technologies, Inc, 501 Allendale RD, Ste 201, King of Prussia, PA 19406. recblid kr2rj63cfbzyl2y28axrxnve0vzzy7
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