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Online Resumes with "Study Start up"
Clinical In-house Monitoring - 13 Years of Experience - Near 08068
Skilled in the planning and implementation of clinical research projects in compliance with ICH-GCP, Regulatory Agencies, and company SOP. Study Start up expert. Proficient in Microsoft Office Applications, CTMS, IVRS/IWRS, INFORM, Medidata Rave. Therapeutic areas: Oncology, Cardiology, Neuroscience, Internal Medicine, including Diabetes. Participated in 3 FDA Submissions, FDA Inspection Readiness and TMF reconciliation
Tags for this Online Resume: Princeton, Study startup, In house CRA, CTA, Inform, Medidata Rave
Nurse Executive, Clinical Research
Using nursing skills, critical thinking skills and clinical research experience of 13 years, I would like to advance professionally by leading a team of engaged researchers.
Ideal Companies: Academic Hospital with engaged physicians
Tags for this Online Resume: Michigan, ethical, professional, energetic, passionate, attentive, nurse, experienced
Clinical Research - 14 Years of Experience
Nursing professional with management experience in conducting phase Ib – IV pharmaceutical clinical trials in Cardiovascular, Endocrine, Respiratory, GI, and Immunology diseases. Broad base knowledge of FDA regulations and Good Clinical Practices for study start-up, execution, and completion using applicable SOPs and site policies and procedures
Tags for this Online Resume: Research Nurse Coordinator, Drug Safety Specialist
Clinical Research - 20 Years of Experience - Near 60601
-Participate in development of new intramural clinical research studies, both for solid tumors and hematology/oncology, reviewed all new protocols, supervised designing case report forms for the new protocols for the solid tumors and hematology/oncology. -Work with the multiple investigators on developing and implementing new intramural oncology protocols and supervised accomplishments with all protocols' requirements. ...
Clinical Trial Assistant, Downingtown
Support Clinical Trials in processing documents from study start-up to study close out.
Tags for this Online Resume: clinical , support, assistant, research, project, study
Clinical In-house Monitoring - 15 Years of Experience - Near 27514
Experienced monitor, study coordinator, study start-up specialist and medical researcher seeking position where knowledge of medical terminology, clinical trials experience, regulatory knowledge, organizational strengths, and strong people abilities can add to a company's overall quality and growth. Since 1998 I have been in Clinical Research. I have a strong background in clinical monitoring, study coordinating and quality...
Clinical Research - 6 Years of Experience - Near 10461
Accomplished Clinical Research Professional with over 6 years’ experience in Clinical Study Manage- ment and hands-on skills in all spheres of clinical study process including but not limited to site manage- ment, study monitoring, all types of site visits, study start up and close out as well as data management. I wish to work with a team that will enhance my clinical research knowledge and broaden my scope.It is fulfill...
Tags for this Online Resume: georgia, Oncology, respiratory, CNS, Texas, Cardiovascular, New york
Clinical Research Project Manager, Regulatory Manager, Study Start-up Manager, Clinical
Clinical Data Analyst/Coordinator
Clinical Data Management Services, with extensive phase I-IV pharmaceutical experience in the following therapeutic areas: Dermatologic, Pathologic, Oncology, Ophthalmic, Infectious Diseases. Excellent analytical skills in data review and experience validation of data base design and study start up. Hands on knowledge of medical clinical research terminology and transcription, (EDC) Electronic Data Capture Experience.
Tags for this Online Resume: Clinical Data Coordinator, Clinical Data Analyst, Clinical Associate, Data Entry Operator, QA , Data Validation, Data Entry, Data Processor
Clinical Data Management - 9 Years of Experience - Near 01821
SUMMARY * I am certified-RAVE Study Builder- Certification Sponsored by Cognizant & Medidata USA. I have 12 years of experience in Project Management, Clinical Data Management, Technical Support and Team Management,Overall 10 years of progressive experience in Clinical Data Management domain from study start up till DBL activities. I am experienced with all aspects of data management including project management, edit check...
Tags for this Online Resume: Management, Data Management, Pharmaceutical Industry, Quality, Quality Control, Team Lead, Document Management, Audit, Training, Quality Assurance
General Manager - 6 Years of Experience - Near 10040
Title Study Start Up Lead II
Tags for this Online Resume: Frisco Tx, Documentation, Injections, Medical, Physical Therapy, Protocol, Therapy, Interactive Voice Response, Management, Voice, Clinical Research, Site Management, Clinical Trials, Oncology Trials, Phase 1-3, Texas, Plano, Dallas
Sr. Clinical Research Coordinator - 14 years Experience -Miami
FMG with 14 years experience working in Clinical Research field from Phase I to Phase IV in multiple therapeutic Areas with vast knowledge of GCP-ICH, Medical Terminology and Regulatory Compliance,Bilingual,Works without supervision or a Team, Detailed and Organized, resolution skills looking forward to join a Pharmaceutical Company to represent it in FL in which my skills can help to enhance the Company Efficacy and Effect...
Tags for this Online Resume: Miami, Florida, Sr. CRC, CRA Entry Level, Study Start Up Specialist, Regulatory Affairs
