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Online Resumes with "Clinical research "
Clinical Research
Tags for this Online Resume: Training, Clinical Research, Research, Management, Oncology, ICH, Protocol, Audit, Data Management, Documentation
Mental Health Therapist
Tags for this Online Resume: Management, Assessments, Custody, Security, Trauma, Audit, Clinical Research, Cms, IDoc (Intermediate Document), psychologist, clinical psychologist, assessment, forensic psychologist, correctional psychologist
Clinical Research - 1 Years of Experience - Near 79414
Dear Sir/Madam, Please see the attached CV to be considered for the position . In brief, I attended the University of Cordoba School of Medicine in Argentina from 1989 to 1995 where I achieved an MD degree in 1995. After my graduation, I moved to Spain where the Secretary of Education of the Government of Spain validated my MD degree within Spain and the European Union. From 2000 to 2003 I did three years of residence withi...
Tags for this Online Resume: pharmaceutical, clinical, trial, protocol, phase
Clinical Research - 10 Years of Experience - Near 80027
Tags for this Online Resume: medical writer
RN,BS,CCM - 30+ Years of Experience - Near 19465
I am looking for a RN position, working in a positive and healthy environment. I am very open to change and would love to add a new skill to my already much experienced career. As an RN of over 30 years, I have traveled extensively and worked in many different healthcare settings. I have been both student and mentor and enjoy being either. I have found that I do best in a fast paced, ever changing environment, filled with c...
Tags for this Online Resume: Data Entry, Clinical Research, Insurance, registered nurse, remote, telephonic, case management, drug safety, heids, quality review, chart auditer, data extraction
Pharmacist - 1 Years of Experience - Near 33334
I am an enthusiastic pharmacist
Tags for this Online Resume: Data General Nova, Nursing, Reconciliations, Cancer, Cardiopulmonary resuscitation (CPR), Chemotherapy, Clinical Research, Critical Care, Health Insurance Portability And Accountability Act, Hepatitis
Molecular Cell Biology / Research Associate
SUMMARY OF QUALIFICATIONS * 4 years of post doctoral experience in molecular neurodegeneration analysis * Demonstrated expertise in cell culture technologies including Primary cells, stem cells, iPS cells, and differentiation to desired cell types * Demonstrated assay development skills for microRNA analysis in neurodegenerative diseases * Demonstrated time management and project management experience with strong team leade...
Tags for this Online Resume: Research, Clinical Research, Quality Control, Pharmaceutical, Quality, Quality Assurance, Support, Technical Support, Inventory, Inventory management, project management
Scientific writer - 8 Years of Experience - Anywhere in the US
I am a highly motivated professional seeking to utilize my technical, educational, creative and interpersonal skills to advance organizational goals and contribute to making real-world impacts in the scientific, pharmaceutical and research industry.
Tags for this Online Resume: Health Care Industry, Research, Pathology, Pharmaceutical, Public Health, Training, clinical, research, pharmaceutical, phase i, regulatory, clinical trials
Clinical Research
Clinical Research - 15 Years of Experience
Tags for this Online Resume: gcp, ich, oncology, clinical, protocol, CTMS, EDC
Chief Executive Officer - 15 Years of Experience - Near 32835
To obtain a challenging position in a high quality engineering environment where my resourceful experience and academic skills will add value to organizational operations.
Tags for this Online Resume: Business Development, Engineering, Management, Persuasion, Planning, Problem Solving, Team Leader, Innovation, Executive Officer, Health Technology Management, Health IT, Academic Administration, Clinical Research, Accreditation, Public Speaking, healthcare
Psychology - 17 Years of Experience - Near 92057
Clinical Assisted Director of Operations in the daily operation of all trials at the Site. Responsible for staffing and training study personnel and planning study start-up activities. Responsible for team performance and annual goal reviews. Responsible for client relationships through obtaining feedback from trial monitors and sponsors. Trials was an outpatient Phase 2-4 clinical research facility with a 4-bed sleep labor...
Tags for this Online Resume: Management, Process Improvements, Risk Management, Clinical Operations, Clinical Research, Research, Pharmaceutical, clinical, phase iv, phase iii, pharmaceutical, quality, clinical QA, GCP, document control, clinical trials, IRB, consent document, essential documents, nonessential documents, SOPs, Work Instructions
