CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "IRB "

Certified Clinical Research Coordinator - 13 Years of Experience - Near 34202

Seasoned Certified Clinical Research Coordinator with 13 years' experience as a CRC, including experience in marketing, advertising, and regulatory document completion and submission. Completed my duties with great attention to detail, compassion, professionalism, confidentiality, and care. Seeking a position in healthcare/clinical research/pharmaceutical industry that will allow me to continue to exercise these skills and ...

Tags for this Online Resume: Clinical Research, Research, Good Clinical Practices, Protocol, Advertising, Documentation, Marketing Management, NPI, Training, Accounts Payable, clinical, trial, phase, gcp, protocol, pharmaceutical, GCP, IRB, CRF, ich, AE, SAE, SUSAR, Inclusion and Exclusion Criteria, ECG, Biological, PK, PG, Substudy, ICF, EDC, Rater, concomitant medications, IP, IP accountability, regulatory documents, master file

Medical Scientist - 14 Years of Experience

Profile: Professional in Clinical Research with Extensive Medical Knowledge and Academic Research Experience Summary of Qualifications Clinical Research Skills * Graduated with Master Degree in Clinical Investigation Sciences, with knowledge and experience in clinical research, clinical trials design, IRB application, informed consent writing, protocol design, and data analysis. As well as knowledge in epidemiology and publ...

Tags for this Online Resume: Cardiology, Progress, Research, Cardiovascular, Medical, Consulting, Data Analysis, Pediatrics, Training, Attention to Detail

Clinical Regional Monitoring - 20 Years of Experience - Near 18929

Seeking an opportunity with a Pharmaceutical, Biotechnology company or CRO as a Senior Lead Clinical Research Associate, Lead CRA, CRA Manager/Trainer (Mentor) and/or CRO Oversight Monitor to employ my 27 years of clinical research monitoring, management skills and CRA mentoring as well as19 years of Respiratory/Pulmonary and Cardiopulmonary critical care clinical medicine. Clinical Research Experience: Projects/Therapeutic...

Tags for this Online Resume: Pharmaceutical, Clinical Research, Research, Rheumatology, Biomedical Industry, Pharmaceutical Industry, Cardiology, Critical Care - Neurology, Critical Care - Respiratory, Neurology, oncology, clinical, phase, gcp, protocol, trial, ich

Medical Office Manager - 5 Years of Experience - Near 27502

QUALIFICATIONS: * Promoted to the Senior CRC position as the youngest individual within the organization due to ambition, diligence, a strong team player with the ability to look at the big picture and plan accordingly. * Developed strong CRO/sponsor/vendor relationships, ensuring continuity and open communications through all phases of the trials. * Continuously reached study goals by collaboration with a diverse populatio...

Tags for this Online Resume: Cardiology, Clinical Research, CMA, Communications, Management, Medical, Project Management, Research, Triage, Research Protocols, IRB, Informed Consent, Mentoring

Clinical Research - 20 Years of Experience - Near 98052

CAREER HIGHLIGHTS * Expertise in innovative technology/Diagnostics: CLIA approved Laboratory Director extensive experience in assay/protocol development in molecular biotechnology. Experience in regulatory compliance, accreditation, credentialing, IRB and AICUC. * Serving as CLIA approved director for five high complexity laboratories. Extensive experience in quality control and quality assurance (successfully obtained mult...

Tags for this Online Resume: Research, Biotechnology, Clinical Research, Compliance, Diagnostics, clinical, Microbiology, Human Resources, Management, Pain Management

Instructional Coordinator - 15 Years of Experience - Near 21122

Profile Dr. Anderson has a doctoral degree in education and 15 years of experience in instructional systems design (ISD), learning technologies and adult learning. Her program management skills have maximized training potential and established highly effective learning solutions in corporate and academic training needs. Dr. Anderson has supervised complex teams comprised of SMEs, technical staff, curriculum staff and contra...

Tags for this Online Resume: Information Technology, Leadership, Management, Training, Applications, instructional designer, education, training, teaching, distance education, online learning, instructional technology

Biologist - 20 Years of Experience - Near 94806

Career Summary * Lab Manager with over 25 years of optimizing efficiencies. * Able to coordinate initiatives (both scientific and administrative) within research laboratories strives to propel professionalism while minimizing the efforts produced within the workplace. * Adept at supporting and collaborating with other team members to implement the most appropriate policies, procedures, and protocols for assignments. AREAS O...

Tags for this Online Resume: Administrative Assistant, Critical Care - Neurology, Neurology, Research, Radiation, Complaints, Water Supply, Adobe, Adobe Acrobat, Adobe Illustrator

Clinical Research - 11 Years of Experience - Near 20774

My goal is to successfully coordinate both the technical and administrative details of any research assignment collaborating with the Principal Investigator to achieve study integrity and objectivity through the successful implementation and completion of protocols and procedures. Self-motivated achiever with over eight years' experience in different areas of research work including Human Participants in Research both for C...

Tags for this Online Resume: Clinical Research, Compliance, Good Clinical Practices, Health Care Industry, Health Insurance Portability And Accountability Act, HIPAA compliance, Pharmaceutical, Research, Training

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

Clinical Research - 15 Years of Experience - Near 27540

SUMMARY Ph.D. in Chemistry with 20 years of academic experience in biomedical imaging and cancer research 5 years of business experience in nutritional science and family financial service. * 17 years of leadership and management experience as principle investigator (PI) of biomedical research teams and multi-team consortium, including academia with private sector collaborations. Managed chemistry, medical physics, bioengin...

Tags for this Online Resume: Research, Biomedical Industry, Cancer, Chemistry, Clinical Research, Engineering, Imaging, oncology, pharmaceutical

Executive Assistant - 20 Years of Experience - Near 15025

ITxM ICD-10 training, Critical Care Medicine * Provided Executive administrative support to the Executive Administrator, Critical Care Medicine * Project management support to the Operations Manager, CRISMA Center * Provided Executive administrative support to the Director, Strategic Planning * Supervision of administrative personnel, 5 direct reports (2 clinical admins/3 research admins) * Managed administrative work flow ...

Tags for this Online Resume: Management, administrative assistant, clerical

Clinical Regional Monitoring - 3 Years of Experience - Near 0000

PROFESSIONAL SUMMARY Clinical Research Professional with various project experience from concept to development. Talents include in-depth knowledge of ICH guidelines SAE reporting and GCP auditing. Integral team-player with excellent communication skills CORE QUALIFICATIONS * Patient Recruitment & Screening * Detailed Documentation * Serious Adverse Event Reporting * Communicating with IRB for study proposal, approval and u...

Tags for this Online Resume: Clinical Research, Data Entry, Research, Audit, Communication Skills, Compliance, Documentation, Excellent Communication Skills, Good Clinical Practices, ICH