Hamilton, NJ
... Experience also includes working on
clinical trial administration database software (InfoEd) and managing data related to
clinical trials. Experience in the Pediatric Research includes working on Tuberous Sclerosis Complex Natural history database ...
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May 22
Rockville, MD
... WORK EXPERIENCE
Clinical Research Coordinator- Hospital for Special Surgery Jun'12-present Dept. of Medicine (PI Dr. Linda Russell) Project: Perioperative Ischemic Evaluation-2
Trial (Poise-2
Trial): A large, international, placebo-controlled, ...
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May 20
Valparaiso, IN
... • Supported
clinical trial in Europe by checking CRO activities and their documentation with European standards. • Trended
clinical data for all patients and made charts for IDE filing with FDA. Coordinated stability program for testing and prepared ...
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May 20
Plainsboro, NJ
... 08536 609-***-**** (Home) ( 973-***-**** (Cell) ( email: abvidw@r.postjobfree.com PERSONAL PROFILE Expertise in
clinical drug
trial and regulatory documentation auditing meeting ICH Guidelines, GCP and SOP compliance, regulatory, and government ...
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May 18
India, Vadodara, GJ
... Working in coordination with Principal Investigator and study team to conduct
trial in accordance with protocol, ICH GCP and regulatory requirement. Organize and participate in all
clinical trial related activities including site qualification visit ...
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May 17
India, New Delhi, DL
... Compilation of Regulatory documents and Preparation of
Clinical Trial Application as per schedule Y and CTD format as per ICH- GCP guidelines. . Submission of all Regulatory documents in DCGI office and collection of approvals for respective studies ...
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May 15
Lincoln, CA
... Professional Experience:
Clinical Research Consultant North Valley Nephrology Yuba City, CA February 2012 to August 2012 I was responsible for protocol evaluation and feasibility including
Clinical trial preparation involving the planning, ...
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May 15
Holbrook, NY
... Performed
clinical trial procedures as outline in the protocol, recruitment, pre-screening, scheduling appointment, informed consent process, vitals, source documentation/ data collects and data entry . Reviewed journals, abstracts & scientific ...
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May 15
Westminster, CA
... Perform internal data audits (10 - 20%) on
clinical trial data entry on a quarterly basis to check quality. Increase knowledge of data process flow, medical terminology and anatomy - attend internal classes/teleconferences. Assist in development of ...
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May 13
Plainfield, IL
... 2003- 2004 Center for Aging, Alzheimer s Disease and Neurodegenerative Disorders, Creighton University, Omaha, NE Clinic and Research Nurse and Research Coordinator Screened
clinical trial patients, maintained all aspects of
clinical trial ...
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Apr 22
Port Saint Lucie, FL
... part in a
clinical trial utilizing having patients inside hyperbaric oxygen tanks while treating them for Carcinoma of Cervix Education 2011 – Present I am in the process of taking a Bachelor Degree through distance learning from Ashford University. ...
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Apr 22
Annapolis, MD
... Processed Serious Adverse Events from
clinical trials. . Ensured FDA and International Regulations (ICH) were followed regarding
clinical trial drug safety . Validated reports were accurate, consistent and completed in a timely manner . Conducted ...
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Apr 22
Richmond, VA
... Scheduling appointment, drug screening for admission into
clinical trial, transcribing labs to CRFs for transmission, maintain medical record. Data entry, carrying out other research- related duties as needed. Minimum 2-5 years' experience ...
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Apr 21
Frankston, TX
... in the company’s history • Baxter Healthcare – Acting Regional Manager while manager was absent, Mentor,
Clinical Instructor and
Clinical Trial Leader • Davis and Geck- Regional Trainer, Product Launch Specialist, Assembled a panel of clinicians ...
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Apr 04
Houston, TX
... Researcher: • Participate in the FDA approved
clinical trials. Reviewing and evaluating prospective patients’ medical records to ensure whether requirements for entry to
clinical trial protocols are met; this would include inclusion and exclusion ...
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Apr 03
Bristol, CT
... CMS guidelines, MCM guidelines, Local Medicare Review Policy for
clinical trial medications for Medicare Part B, attend CAC conferences where comments from physician and representatives of specialties meet quarterly and referrals to fraud. Review of ...
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Apr 01
New Orleans, LA
... Services Area 2007-2008 Coordinated research operations within LSU Health Science Center as well as pharmaceutical and
clinical trial companies Administration of schedules and business transactions and electronic grants Managed database of
clinical ...
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Apr 01
Seal Beach, CA
... E ste r Sie ***** ********* ** (310) ***-**** Seal Beach, CA 90740 abqxno@r.postjobfree.com EXPERIENCE University of Southern California, General Surgery May 2007 Nov 2012 Los Angeles, CA
Clinical Trial Specialist • Participated in over 60
Clinical ...
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Mar 29
Loma Linda, CA
... E ste r Sie ***** ********* ** (310) ***-**** Seal Beach, CA 90740 abqxnn@r.postjobfree.com EXPERIENCE University of Southern California, General Surgery May 2007 Nov 2012 Los Angeles, CA
Clinical Trial Specialist • Participated in over 60
Clinical ...
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Mar 29
Farmington, CT
... Conduct Risk assessments and
Clinical trial data analysis. and prepare audit report, Periodic audit plans, document non conformities, observations and Noteworthy efforts identified during audit process, recertification plan and expense report. ...
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Mar 28
