CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with " O "

supervisor housekeeping department

OBJECTIVES • To find a relevant and challenging position in an enabling corporate environment where my learnt and inborn skills would be an asset to my organization. • To have a job that will offer an opportunity for personal and career growth, skills acquisition and job enrichment while being productive.

Tags for this Online Resume: h, i, l, t, o, n

tecniques machine operator minings

Network Engineer

Ideal Companies: dell, hp, it

Admissions Director

MBA

TO ATTAIN THE HIGHEST POSITION IN AN ORGANIZATION

Tags for this Online Resume: DOEACC 'O' LEVEL, AUTOCAD, MS OFFICE, WINDOW 7, XP, VISTA

Baggage Porter

O

Medical & Clinical Laboratory Technologist

Senior Programmer Analyst - 25 years experience in COBOL, PL/1, CICS, DB2, IMS/VS DB/DC, DL/1, BTS, SQL, IDMS/R, OLQ, ADS/O, VSAM, MVS/ESA, VM/DOS/VSE, TSO/E SPF, VM/CMS, QMF, SPUFI, JCL, IDCAMS, CLIST, REXX, EXEC, PANVALET, MICROFOCUS, FOXPRO, CULPRIT, E

Programmer, Developer, Analyst, Production Support Analyst, Team Leader, Quality Assurance and Test Analyst.

Attorney

Legal work

Construction Carpenter

CTA

Seeking for a challenging career in a progressive organization offering the opportunity for contributing my skills services to the organization and personal growth and to work sincerely with maximum effort using best talents and with a challenge to achieve required goals and targets, abiding to the decisions of seniors and to earn a good reputation what ever required.

Tags for this Online Resume:  Develop, maintain and manage appropriate study documentation,  Developing, writing and presenting the clinical trial protocols,  Initiate, maintain and reconcile Trial Master File.,  Monitoring the trial throughout its duration which will involve visiting the Study centers on a regular basis to check the patient data in the case report forms (CRFs) and to sort out any problems which may arise.,  Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other Data collection tools by careful source document review Monitor data for missing of implausible data.,  Complete Serious Adverse Event (SAE) reporting, process production of Reports, narratives and follow up of SAEs and managing the clinical data intermilitently as per 21CFR USFDA guidelines,  Monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP and ICH Guidelines.,  Independently perform CRF review; query generation and resolution against established data review guidelines on client data management systems as assigned Perform other duties as assigned by management., , maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned

Sales Assistant