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Online Resumes with "EDC"
Clinical Research Coordinator - 3.5 Years of Experience - Near 30338
Tags for this Online Resume: Diabetes Mellitus, Audit, Cardiopulmonary resuscitation (CPR), Clinical Research, Diagnostics, Documentation, Health Insurance Portability And Accountability Act, Oracle, Oracle Clinical, Protocol, Clinical Research Associate, Chronic Disease, EDC
Clinical Research - 10 Years of Experience - Near M1T3N
SUMMARY: * NIH trained Study/Site Coordinator with 10 years of experience in clinical research coordination and administration. * Demonstrated ability in coordinating & implementing Network / Pharmaceutical / Investigator-driven multisite Phase I - IV clinical studies. * Adept in liaising with internal and external stakeholders.
Tags for this Online Resume: Protocol, Clinical Research Associate, Infectious Diseases, ICHGCP, Logistics of study material, Monitoring, Data Entry, Team Lead, Essential Documentation, Informed Consent, SOPs, Coordinator, Regulatory, QA/QC, Source Docmentation, CRF's, TMF, EDC, Toronto, Contracts, SAE
Clinical Research - 2 Years of Experience - Near 77449
HIGHLIGHTS OF QUALIFICATIONS: * RN with close to 2-years experience in clinical trials monitoring * Knowledgeable of clinical trial procedures and approval processes. * In-depth knowledge of ICH GCP guidelines and FDA regulations * Conversant with Design and Review of case report forms (CRF) * Conversant with Site Monitoring visits (PSVs, SIVs, IMVs and COVs) to meet study expectations. * Clinical and post-marketing safety ...
Tags for this Online Resume: Direct Patient Care, DRESSING CHANGES, Medical, Patient Care, Suctioning, Surgical, Wound Care, Acquired Immune Deficiency Syndrome (AIDS), HIV, Monitoring
Clinical Research - 8 Years of Experience - Near 85748
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.
Tags for this Online Resume: Scottsdale, Clinical Research, Compliance, Clinical Research Coordinator (CRC), Device Trials, Documentation, Clinical Trial, Medication Trials, Data collection, Microsoft, Electronic Data Capture (EDC), Regulatory submission
Clinical Regional Monitoring - 18 Years of Experience - Near 08053
Tags for this Online Resume: Clinical Research, monitoring, Cancer, Prestudy, initiation and close out visits, Inflammatory Diseases, Cardiovascular, regulatory review, Good Clinical Practices, New Jersey, Phase I - III Clinical trials, EDC, drug accountability, infectious diseases, laboratory and study supply, IRB documentation
Clinical Research
Clinical Research Associate with experience in both pharmaceutical and medical device clinical trials, possessing strong communication skills with sound analytical and problem solving techniques. Demonstrated ability to work independently and in a team environment. Experienced with electronic data capture (EDC) review, entry and query resolution. Skilled in performing clinical trials activities (including site selection, de...
Case Manager - 1 Years of Experience - Near 21224
SUMMARY: 30 years Clinical Research experience and home-based monitoring experience 12 years Oncology monitoring experience 12 years Pediatric Nurse experience 10 years Inform EDC experience and 6 months IMedidata experience 4 years as CRA trainer/mentor 3 years as Local Site Liaison/co-Clinical Monitoring Lead/Clinical Monitoring Lead THERAPEUTIC AREA EXPERIENCE: Oncology-12 years Non-Small Cell Lung-Phase III Colon-Phase ...
Tags for this Online Resume: Audit, Protocol, Clinical Research, Research, Nursing, Management, Monitoring, Therapy, Oncology, SAN (Storage Area Network)
Clinical Research - 15 Years of Experience - Near 92880
ACCOMPLISHMENTS * Worked with 50 different sponsor and CRO companies on various GI studies * Managed Bunion investigational study with 300 patients. * Three FDA audits without 483. * Met all recruitment targets within required study timeframe * Managed regulatory binder for studies, post start-up * In depth knowledge of Microsoft packages ( Word, Excel and power point) Experienced with Oracle, Inform, Medidata eDC programs ...
Tags for this Online Resume: Clinical Research, Oncology, Research, Computer Aided Software Engineering, Good Clinical Practices, Medical, Microsoft, Microsoft Excel, Microsoft PowerPoint, Microsoft Word
Clinical Research - 8 Years of Experience - Near 60169
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...
Tags for this Online Resume: 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
Clinical Data Management - 18 Years of Experience - Near 18938
SUMMARY Expert level Project Management, Data Management & Standards, Database Analysis and Application Design with Oracle Applications in the Pharmaceutical Industry. Extensive knowledge of Clinical Life Sciences Domain. Experience working for Sponsors, Biotech, Service Provider and CRO. Leadership capabilities to manage complex projects from project initiation to implementation. Delivery experience between the Business an...
Tags for this Online Resume: Data Management, Oracle Clinical, Structured Query Language, Applications, Pharmaceutical, Protocol, Consulting, Oracle Inform, Central Designer, Standards Project Management, Oracle Database, Clinical Information Systems, Electronic Data Capture (EDC), SQL Developer, SDTM Mapping, CDISC
Pharmacist - 14 Years of Experience - Near 19115
Experienced with Oracle Clinical, ClinTrial, ARGUS 7.0.7 databases, MedDRA 20.0, Who Drug coding systems, and EDC system.
Tags for this Online Resume: Management, Insurance, Managed Care, Coding, Data Entry, Data Management, Documentation, Pharmaceutical, Protocol, Regulatory Affairs
Clinical Research - 12 Years of Experience - Near 78254
SUMMARY OF QUALIFICATIONS * Managed Phase I -IV and observational Clinical Research Trials for HIV/AIDS, HIV Vaccine trials, HIV and Hepatitis, Infectious Diseases, Hyperlipidemia, Diabetes, Renal CKD, Secondary Hyperparathyroidism, Vitamin D Deficiency, Diabetic Nephropathy, Allergies, Asthma, and Immunology, Hepatic therapeutical area, from HBV, HCV, Fatty Liver, Cirrhosis in the Liver, medical devices. * As an inhouse mo...
Tags for this Online Resume: PEDIATRIC, Pharmaceutical, Surgical, C Programming Language, Data Entry, Hepatitis, Hepatitis C, Research, Therapy, Cardiovascular
