Consummate professional with 10 years of experience working in diverse therapeutic areas, with experience in leading Data Managers working in both drug and medical device trials. Aspiring for a position which has a blended responsibilities of leading the project and Data Managers.
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Clinical Project Manager, Clinical Data Manager, Rave, San Diego, San Francisco, California, CRO
SUMMARY OF EXPERIENCE: CRA Experienced CRA with more than 15 years in clinical trials and extensive experience in management of phase II to IV clinical drug trials to include a device trial. Five years as a Study Coordinator in a Cardiology Research Clinic. Together with medical background as a Registered Nurse possess far-reaching knowledge spanning several therapeutic areas including Cardiovascular, Oncology, Neurology, M...
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Monitoring, Management, Project Management, Device Trials, Clinical Research, Oncology, Research, Training, Documentation, Exposure to Many Therapeutic Areas
Initialized Managed stable and equine healthcare, trained jumpers, started young horses under saddle. training under saddle and exercised horses of various disciplines to include: jumpers dressage polo and racing. Prepped and exhibited thoroughbred yearlings for sales pavilion. Assisted in endoscopy exams and radiological soundness exams.
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Scottsdale, Clinical Research, Compliance, Clinical Research Coordinator (CRC), Device Trials, Documentation, Clinical Trial, Medication Trials, Data collection, Microsoft, Electronic Data Capture (EDC), Regulatory submission
Professional Summary A certified professional Clinical Research with 4 years of experience in Clinical Research coordination and a year experience as Clinical Study Associate. Expertise in QC of documents, remote Monitoring and supporting the management by handling the tasks of multiple clinical research studies managing eTMF's & designing Clinical Portfolio's from Sponsor end. Expert in liaising between different departmen...
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Document Management, Monitoring - Remote and onsite, Clinical Research coordinator, Device trials, clinical Research, Project Management, QC and QA, Pharmacovigilance, Ethics and compliance, regulatory, Clinical study Associate, Multiple therapeutic areas experience, Phase 1-4 trials, Audits and Inspection readiness, Multiple software and application experience - Veeva VAULT , Impact , Quest , Sentinel,Tesla, EDC experience- RAVE Medidata, IRT system experience Clinpace , Endpoint
CURRICULUM VITAE: Sharon Woodruff
Team excellence instructor, facilitator, and trainer. Proven managerial, interpersonal, and training skills.
Work History
Title: Senior Clinical Research Associate
Company/Location United BioSource Corporation Kansas City, MO/Regional United States
Dates July 2014 - January 2015
Accountabilities
Implement and monitor clinical trials for medications and devices to ensure sponsor and invest...
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South Carolina, Training, New Hire , Business, Education, Postsecondary, Excellence
