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Online Resumes with "Clinical trial "
Clinical Regional Monitoring - 0 Years of Experience
To obtain a fulltime/permanent Clinical Research Associate position having 10 plus years clinical trial experience as a Clinical Research Associate and laboratory Quality Assurance Auditor excellent organization and communication skills travel expertise superior clinical laboratory experience and knowledge coupled with the desire to manage, mentor and train others.
Tags for this Online Resume: Management, Audit, Hematology, Microbiology, Venipuncture, Banking Industry, Blood Bank, Emergency Medicine, Trauma, Pathology, clinical, gcp, protocol, trial, pharmaceutical, ich, phase
Clinical Research
Tags for this Online Resume: Microsoft Excel, Microsoft Access, Project Coordinator, Protocol, Research, Training, Adobe, Certificate Authority, Compliance, Data Entry
Quality Coordinator - 0 Years of Experience
Summary: * Extensive experience in clinical data management, pharmaceutical, and device research industries. * Experience working with Adverse Event Reporting and Medical Device Reporting. * Strong analytical, problem resolution, and project management skills. * Proficient in monitoring and managing record retention timelines for all clinical and regulatory documents and assistance in the preparation and review of documents...
Tags for this Online Resume: Data Entry, Database, Distribution, Filing, Documentation, Licensing, Medical, Microsoft Access, Regulatory Affairs, Research, clinical research
Quality Coordinator - 10 Years of Experience - Near 35173
Tags for this Online Resume: ICD-9, Insurance, Surgical, Coding, Documentation, Data Management, Data Queries, HIV, Management, Oncology
Clinical Quality Assurance
Tags for this Online Resume: Management, sheets, Support, Legacy, Protocol, Surgical, Documentation, Health Insurance Portability And Accountability Act, MDR, Quality Assurance
Clinical Research - 15 Years of Experience - Near 15135
Profile: Medical background with extensive research, quality improvement, regulatory, consent writing, creation of protocol-specific tools for physicians and coordinators, local IRB and external/commercial IRB, Institutional Review Board Staff, institutional liaison with all external IRBs, HTML coding of all active AHN studies for our AHN.org research site Personal Qualifications: Excellent communication skills, team player...
Tags for this Online Resume: Pharmaceutical, Research, Coding, Database, Documentation, Health Insurance Portability And Accountability Act, HTTPs, Human Resources, HyperText Markup Language, Information Technology, clinical trials, research, pharmaceutical, regulatory, clinical, cro, phase i, phase ii, phase iii, phase iv
Clinical Research - 11 Years of Experience - Fort Wayne
I have been a Registered Nurse for 25 years, working in Clinical Research for the past 11 years. I am a Senior Clinical Research Coordinator looking to expand my career into the role of being a Clinical Research Associate or Project Manager. I am open to full-time employment or contract work.
Tags for this Online Resume: Clinical Research, Corporate Training, Documentation, Recruiting, Research, Training, Allergy, CENTRAL LINES, Injections, Nursing, Project Management, Clinical Research Coordinator, Clinical Research Associate, Clinical, pharmaceutical, CRO, phase I, Phase II, Phase III, Phase IV, Regulatory, Clinical Trials, Research Coordinator, Project Lead, Clinical Research Lead
Pharmaceutical Industry positions - 5 Years of Experience (academia) - Charlotte, NC
I'm a Ph.D. graduate with 5-year research experience in the drug discovery and development field, and actively looking for an entry-level position in the pharmaceutical industry. Equipped with a Bachelor's Degree in Science from China Pharmaceutical University and a Ph.D. in Pharmaceutical Sciences from University of Arkansas for Medical Sciences, I am well-prepared to align my skill set with any position that requires a pr...
Tags for this Online Resume: High Performance Liquid Chromatography (HPLC), Pharmaceutical, Pharmacology, Phoenix, Research, Analytical Chemistry, Pain Studies, Pharmacokineitcs, Regulatory Affairs, LC/MS, Drug discovery and development, R&D, clinical trials, research, Quality Control, Quality Assurance
Sr. Clinical Research Associate - 22 years Experience - remote - Austin, TX
A top-performing Senior Clinical Research Associate with extensive experience in clinical research, GCP, ICH, Regulatory, and clinical site management/monitoring. Solid background in critical care nursing for in-depth understanding of medical terminology for records review. Highly skilled in spearheading internal teams through clinical research and document management to ensure accuracy and adherence with study specific str...
Ideal Companies: Pharmaceutical, Biotech, Medical Device, CRO
Tags for this Online Resume: Clinical Research, Management, Protocol, Research, Documentation, Medical, Allergy, Monitoring, Reporting Tools, Cardiology, clinical, trial, gcp, protocol, pharmaceutical, regulatory, medical device, CNS, EDC, contract, remote, CRO
Pharmacist - 22 Years of Experience
ACCOMPLISHMENTS * Coordinated and conducted clinical and academic research * Coordinated and actively participated in teaching clinical pharmacology course to Internal Medicine staff * Developed a clinical module for pharmacy staff * Developed automatic substitution protocols, resulting in significant dollar savings, reducing length of stay and minimizing bacterial resistance * Established cost-effective formulary * Assesse...
Tags for this Online Resume: Patient Care, Support, Management, Budgeting, Clinical Programs, Purchasing, Pharmaceutical, Clinical Research, Consulting, Research
Clinical Research
Tags for this Online Resume: Protocol, Documentation, Management, Query, Clinical Research, Research, Distribution, Project Management, Project Manager, Clinical Management
Clinical Regional Monitoring - 15 Years of Experience - Near 75219
Professional Summary Accomplished and energetic Senior Clinical Research Associate with a solid history of achievement in monitoring clinical trials. Motivated leader with strong organizational and prioritization abilities. Performed lead study duties to include trip report review and expense reporting. Mentored junior level CRAs and provided feedback and constructive critiques. Interested in senior positions as a research ...
Ideal Companies: Allergan, Bayer, CMED, Novartis, Pfizer, Paidion Research,
Tags for this Online Resume: Clinical Research, Research, Medical, Medical Records, Monitoring, Documentation, Protocol, Complaints, Nursing, Ophthalmology
