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Online Resumes with "clinical trial "
Clinical Research - 4 Years of Experience - Near 60009
SUMMARY * Quality focused Clinical Research professional, with nearly 4 years of experience, and exposure in, Research & Development, Quality Checking, Monitoring, Regulatory Affairs and Document Management
Tags for this Online Resume: Regulatory Coordinator, Clinical Trial Management, Document managment, Quality Checking, Monitoring, Management, Data Entry, Protocol, Regulatory Affairs, Clinical Research, Compliance, Document Management, Email
Clinical Research - 20 Years of Experience - Near 33498
As the Director of PSRI, I specialize in the analysis and restoration of Complex Multi Therapeutic Clinical Programs with a minimum of Invasive change to the Sponsors Design. I concentrate on complex, Pharmaceutical, Biologic, Medical Device, Vitamin/Supplement and Food Clinical Research. I'm experienced and well versed in all FDA/GCP & ICH requirements for conducting Phase I thru IV research. I have worked on all phase...
Tags for this Online Resume: Documentation, Pharmaceutical, Clinical Operations, ICH, Management, Protocol, Audit, Clinical Research, Good Clinical Practices, Medical
Clinical Research Associate II - 7 Years of Experience - Santa Clara
Seeking a position in Pharma as well as Medical Device in which utilized my experience to manage investigative sites, monitor and oversee regulatory compliance in clinical trials.
Tags for this Online Resume: CTMS, EDC, GCP, ICH, CRO, FDA, Medical Device, Monitoring, Management, Compliance, Data Management, Cascading Style Sheets, Clinical Research, CSS, Data Queries, Distribution
Systems Support Analyst- 3 Years Experience in CRO field
I aspire to progress my career by utilizing and expanding upon my knowledge and experience in the CRO field. Clinical trial research is challenging, fascinating, and vastly important to the many individuals who benefit from pharmaceutical development. I look forward to furthering my career by contributing my expertise of SQL developer, knowledge of the design of clinical trials, and excellent client relation and teamwork ...
Tags for this Online Resume: SQL Developer, MS Excel, Database Updates, MS Access, Data Management, Research
Clinical Research Scientist
My goal is to leverage my strong scientific, medical, and clinical trial experience as the foundation for building a career in Pharmaceuticals and Biotech companies. The positions I am interested are Clinical Scientist, Drug Safety Scientist, PV scientist, Non-MD Study Clinician, Clinical Trial Manager and other opportunities in San Francisco bay area. I am open to both permanent and contract positions.
Tags for this Online Resume: San Franciso, Oncology, Research, Trials, Management, Scientist, Pharmacovigilance, GCP
Product Complaints Specialist
Seeking a position which will allow me to execute as well as challenge my current skill set resulting in performance growth and advancement. Exceptional verbal/written communication, organizational, leadership, analytical, and interpersonal skills
Ideal Companies: Biomedical, Biotechnology, Healthcare compliance
Tags for this Online Resume: compliance, Regulatory
Clinical Research - 15 Years of Experience - Near 90001
I am seeking a position in Clinical Trial Management or as a Project Manager per my previous US and international experience.
Ideal Companies: Pharmaceutical or Biotech
Tags for this Online Resume: Oncology, Orthopedics, Surgical, Clinical Research, Management, Medical, Medical Affairs, Diabetes, Cardiovascular, Women's Health, Clinical Trial Management, Regulatory, Medical Writing, Microsoft, CTMS
PhD with Clinical Research Training and 5 years research experience - seeking Clinical Research and MSL related positions
Highly driven and dynamic scientific professional, strategic and analytical in processing and integrating scientific and clinical information. Fast learner who thrives under challenging and demanding situations with steep learning curves. Excellent written and oral communicator with an established record of effective and influential presentations at key international conferences and won best oral presenter/presentation awar...
Ideal Companies: Roche, Johnson & Johnson, Pfizer, Genentech, GlaxoSmithKline (GSK), Sanofi, Novartis, Bristol-Myers Squibb, Abbott, Bayer, Merck & Co., AstraZeneca, Amgen, Lilly
Tags for this Online Resume: Scientific Expertise, Written and Oral Communication, Leadership qualities, Time Management, Clinical Research, Scientific Liaison, PhD, Relocatable
Quality Manager - 16 Years of Experience - Near 98012
ACCOMPLISHMENTS Lead teams to achieve fastest clearance times for the Ultrasound business unit outpacing all other Medical Device business units in Philips Regulatory Affairs Professional Society (RAPS) Regulatory Affairs Certified (RAC) American Society for Quality Certified Biomedical Auditor (CBA) ISO 13485:2003, ISO 9001:2000, and ISO 14001:2004 Lead Auditor Certified Implemented Japanese Ministerial Ordinance No.169. A...
Tags for this Online Resume: Quality System, Regulatory Affairs, Compliance, Clinicals, ASQ Biomedical Auditor, RAC, ISO13485, Risk
Clinical Research
Tags for this Online Resume: Project Manager, Clinical Trials
Clinical Regulatory Affairs - 20 Years of Experience - Near 92694
I love what I do. Although, I have a broad knowledge of Clinical Trials and the desimenation of these trials/studies I love being a part of from first launch to final result. To continue in a job that enables all of my capabilities and to manage/direct the dynamic teams it takes to complete this effort is of great reward and love helping and giving back to our patients we represent.
Ideal Companies: Pharmaceutical companies
Tags for this Online Resume: manager, director, clinical trials, GCLP, ICH, Liaison, Client, Clinical, Site Manager, global, audits
Clinical Research Associate - Entry level - Waterloo
Driven, dynamic, and detail oriented. Trained in ICH/GCP guidelines to monitor clinical trial processes. Actively seeking an entry level CRA position within clinical trial programs.
Tags for this Online Resume: ICH/GCP, Clinical Research, SOPs, Case Report Forms, Microsoft Office Suite, Phases I - IV trials, Recruitment
