Clinical Research Specialist

Tampa General Hospital- C.O.R.E Tampa,Florida

- New Port Richey , FL Work History Clinical Research Specialist , 10/2020 to Current Tampa General Hospital - C . O . R . E - Tampa , FL Financial Research Coordinator III , 01/2017 to 06/2020...families about clinical trial process Provide compassionate care and respectful service to trial volunteers during their research experience Demonstrate knowledge and understanding of clinical trial protocol...Investigators , I have studied many research trials in Oncology . My experience have allowed me to gain solid knowledge of all stages of drug development , safety and clinical trial management from PSV , Start

Clinical Research Specialist

University of Wisconsin School of Medicine and Public Health New York,New York

Compassionate Efficient and reliable team player Adaptable Patient - focused care Work History Clinical Research Specialist Feb 2016 - Jun 2016 University of Wisconsin School of Medicine and Public Health Madison

CLINICAL RESEARCH SPECIALIST

UNC Lineberger Comprehensive Cancer Center Durham,North Carolina

Current UNC Lineberger Comprehensive Cancer Center Chapel Hill , NC January 2009 to Current CLINICAL RESEARCH SPECIALIST Lead CRA on 16 accruing studies ranging from Phase I to Phase IV Pharmaceutical , In...Radiation Oncology Department SOCIAL RESEARCH ASSISTANT This position was created to combine the tasks of a Project Manager with the role & responsibilities of a Clinical Research and Regulatory Associate in the... , outline expectations for study Start Ups . Create and maintain a research chart for each treated patient by compiling clinical data from a variety of sources . Complete data forms and resolve data

Clinical Research Specialist

Memorial Sloan Kettering Cancer Center Queens,NY

York , NY Bachelor of Arts : Biology , Public Policy Work History 02/2020 - Current Clinical Research Specialist | Memorial Sloan Kettering Cancer Center - Commack , NY Screened patient records...protocols covering patient care and clinical trial operations . Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols . 09/2017 - 02/2020...medical facilities Worked quickly and efficiently with clinical teams to solve problems and to ensure that clinicians' needs were met Audited clinical documentation with great attention to detail to ensure

Clinical Research Specialist

Quintiles Plymouth,Massachusetts

background in FDA clinical research guidelines Experience with e CRF platforms : Medidata and Clinform Excellent communication skills . Professional Experience Clinical Research Specialist August 2011...Quintiles － Research Triangle Park , NC Lead clinical teams on Associate Clinical Scientist February 2002 to August 2011 Quintiles － Research Triangle Park , NC Lead clinical portion of Clinical Trials...Senior Clinical Research Associate February 1998 to September 2000 Quintiles － Boston , MA Mentored fellow Clinical research Associates to perform all monitoring visits . Senior Clinical Research Associate

Senior Clinical Research Coordinator

University of Pennsylvania Philadelphia,Pennsylvania

periodically as per the protocol . Experience with PK/PD and toxicological data . Medacta Clinical Research Specialist | Erie , PA 11/2018 to 12/2019 Experience with management and generation of reports...referrals to locate potential research study participants . Wayne State University Clinical Research Coordinator | Detroit , MI 08/2016 to 10/2018 Management of clinical trial study by recruiting Medical...Certifications Certified - GCP/ICH Medidata Certified Experience University of Pennsylvania Senior Clinical Research Coordinator | Philadelphia , Pa 01/2020 to Current Assist program managers with initiating

Clinical Writer

GE Healthcare New Berlin,Wisconsin

2006 Senior Clinical Research Specialist Irvine , California Supervised and mentored junior clinical research associates . Appeared before the Japanese MHLW for the GCP audit of an IDE clinical study that...Maintained regulatory documents in the Clinical History File and at the clinical site . Collaborated with investigators , site management organizations , and clinical research coordinators . Collaborated with... Services February 2010 to September 2010 Sr . Clinical Research Associate , Consultant Irvine , CA Managed Phase I clinical studies in the Clinical Pharmacology and Quantitative Sciences department