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Online Resumes with "clinical researcher "
Clinical Research - 10 Years of Experience
Clinical Research - 6 Years of Experience - Near 80918
Pursuing a challenging career in an organization where I can apply my talents and education in a medical/scientific-related field. Qualification Highlights Proficient use of Databases: iMedidata RAVE, RTOG, GOG, Inform, Oncore, CTSU, SWOG, Clincapture. Oversee RNs are strictly following X-Chart requirements of study protocols. Reviews Expectancy Reports of all associates in our department to ensure data timelines are met. R...
Tags for this Online Resume: Clinical Research, Research
Clinical Research - 0 Years of Experience
You shouldn't have to read my entire resume to know I'm the one!
I absolutely enjoy what I do and look forward to work every week. I know there will be challenges and problems that my team and I will have to solve. I enjoy this career because every day is different. Every study requires a different amount of care and expertise/experience. I love the organization that comes with this career. I love having my own studies and organize documents according to company SOP as well as my own way...
Ideal Companies: Any Biopharma Company (start-up, or young companies) in Phase 1 or 2 of their studies
Tags for this Online Resume: Instant Messaging, Data Analysis, Document Management, Good Clinical Practices, Good Laboratory Practices, Management, Medical, Medical Terminology, Microsoft, Microsoft Excel, Data Entry, Site Feasibility, Trial Master File Audit, Trial Master File, Routine Monitoring Visits, Bilingual, IWRS Systems, DSMB, analysis of PK data from different generations of Japanese subjects, Receiving Plasma samples and storing them in freezers, Urine collection and UA testing, Phlobotemy, ECGs, Dosing, Writing Visit Reports, Query data sheets, Resolving Queries within the SOP allotted time frame, Pippetting Fluids and shipping off with appropriate courier., CRA visit matrixes, Reporting numbers and statistics to Project Manager and Operations Manager, Reviewing Source Documents and making original source documents according to procedures in the protocol, Protocol review sessions, QA sessions daily with a volunteer from each department to go over daily data and tasks to make sure none were missed, Call subjects and perform AE checks according to timelines on protocol, Send critical documents to sites directly or through CRAs as demanded., Make progress matrices of site visits and site reports, Send reminder emails for upcoming visits for CRAs and internal deliverables, Coder
Clinical Research
Clinical Research - 15 Years of Experience - Near 75089
I have been doing contract work For the last 2 years In house site audits Getting site ready for FDA audits
Tags for this Online Resume: Management, Project Management, Documentation, Training, VITAL SIGNS, Protocol, Audit, Banking Industry, Best Practices, Biomedical Industry
Clinnical Research Associate
Contract Medical Writer
Summary Work Experience: Strong background in medical writing and biotechnology product and services development, with a solid publication record in the peer-reviewed medical literature in addition to biotechnology analyst articles-an unusual combination of medical writing expertise, analytical skills, data analysis, management experience, and medical knowledge. Participate in pre-clinical, clinical, and commercial research...
Tags for this Online Resume: Business Development, Cancer, Clinical Research, Medical Writer, regulatory science, biologics, drugs, medical device
Clinical Research
Clinical Research
Clinical Research - 8 Years of Experience - Near 30024
Tags for this Online Resume: phase I, Oncology, pediatrics, data , monitoring , SAE, regulatory, clinical team
Life Scientist
Accomplishments Identified and established productive scientific collaborations served as a scientific liaison between academic institutions, and contributed to and led multiple research programs. Proven experience in developing and planning research studies, writing scientific articles for peer-reviewed publication, developing standard operating procedures (SOPs), and presenting complex/technical information to the medical...
Tags for this Online Resume: Research, Analytical Skills, C Programming Language, Cancer, Clinical Research, Computer Aided Software Engineering, ELISA, GloboMax PDx Pharmaceutical Development Expert Tools, ICH, Imaging
