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Online Resumes with "source documents review"
I have completed a Masters program in Biotechnology. I have keen interest in Clinical Research and Regulatory Affairs. I am looking for an entry level Clinical or Regulatory position. I have research site coordination experience in the areas of Rheumatology and Pain research. I am also ICH and GCP certified.
Tags for this Online Resume: CRF writing, patient follow up, administering informed consent form, administering psycometric scales, source documents review, Reporting SAE’s, Pre-screening and recruiting patients, -Submitted documents to the Ethics Committee, Rheumatology, Pain
AccountingMatthew Rippin 168 Archibald St. Cincinnati, OH 45244 (513) 606-8190 email@example.com __________________ Objective Accountant. Summary of Qualifications Accountant Maintained accounts payable records. Filed developing capital project procedures and audit controls. Developed and maintained capital project files. Reviewed capital projects purchases. Assisted in development of computer progra...
Tags for this Online Resume: Maintained accounts payable records. Filed developing capital project procedures and audit controls. Developed and maintained capital project files. Reviewed capital projects purchases. Assisted in development of computer programs for maintaining capital , Reconciled various expenditure reports to source documents. Reviewed procurement documents and invoices for accuracy. Prepared routine entries and posted financial transactions. Reconciled entries and internal ledgers to financial system reports. Assisted
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
I am seeking for a stable and well established company that is growing. Also,what I am looking for in a new job is for employers that care about their employees and acknowleges them for their good hard work. I would also hope that good training is provided so that the individual such as myself can be productive for the company and contribute towards it's success rate. I would also hope that it was a warm welcoming environm...
Tags for this Online Resume: Dallas, GCP, Informed Consent, Data Management, Archiving, Microsoft Office, FDA, Accounts Payable, Internal audit preparation, Contract management, Ancillary, Query resolution, Quality assurance, Source document review, Administrative Assistant, Billing, Business Development, Clinical Research, Financial Services, Management, ICH, iMedidata, Oracle, Inform, PeopleSoft, Salesforce, Contract/Grant Management, Concur
SUMMARY OF CLINICAL EXPERIENCE Eleven years' experience as a CRA which includes 2 years as a Lead CRA in clinical trial monitoring, including study start up, study initiation through closeout, as well experience in International, and Domestic studies. Provide on-site clinical trial monitoring and full site management at investigational sites in the conduct of Phase II-IV clinical trials. Recruited and trained CRA (s), inves...