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Online Resumes with "Subject safety"
I have had a variety of careers in the health, mental health, teaching, and research fields
My previous career involved monitoring clinical research studies. I would like to continue in the field of research and welcome the idea of travel to achieve this.
Tags for this Online Resume: clinical research monitor drug studies, mental health professional service coordinator, children's therapist
Clinical Trial Specialist / CRA _ Home based
Achieve the successful of clinical trial and ensure the subject safety and the high data quality by working closely with each clinical site and ensure that all the tasks are being conducted in accordance with the clinical trial protocol , ICH GCP guidelines and local regulations.
Research Coordinator, Atlanta, GA.
To use my experience and knowledge to ensure subject safety while obtaining quality data to help move new pharmaceuticals through the FDA approval process for a site/company who appreciates and supports my contributions and efforts.
Director, Business Development Clinical Research IRB- 14 years Experience- Seattle/Portland/Denver
Senior marketing and client development executive with 14 years experience in clinical research. I am looking for continued growth as a research professional leading project teams and staff in support of strategic business goals. As a leader in the development and maintenance of productive client relationships, I have been recognized for expanded customer utilization of products and services with a focused customer-centric...
Ideal Companies: Quintiles, Huron Consulting, Roche, Genentech, PharmaLink Consulting, Icon, Covance, PRA International, AAHRPP
Tags for this Online Resume: Account Management, Client Services and Develpment, Marketing, Project Management, Presentations, Budgeting, International Business, Team Leadership, Process Improvement, Training/Development, Performance Management, Business Development, Operations Management, Branding, Vendor Relations, Clinical Research Regulatory Compliance, Federal Regulations
Clinical Research - 20 +Years of Research Experience - Near 30519
Secure a position that allows me to advance strategic and operational efficiencies, improve data quality, assure subject safety mitigate risk through implementation of a risk based approach to trial conduct. Working closely with a cross functional team to attain process improvements, assure compliance reduce trial cost of conduct.
Ideal Companies: Medical Device, CRO and Pharmaceutical Companies
Tags for this Online Resume: Organized high energy, quality and compliance, Effective communicator, Problem Solver, Leader/Trainer/Mentor, Medical Writer, Project Management, Critical Thinker
Clinical Research - 6 Years of Experience - Near 75287
PROFESSIONAL SUMMARY: A CRA with strong eye for detail and exceptional ability to interpret and follow instructions Possesses the ability to collect accurate data in line with client specifications excellent analytical and organizational skills knowledgeable in FDA regulations, GCP/ICH guidelines, seeking to join an organization that makes research subjects' safety its first priority. CORE QUALIFICATIONS: * Over 5 years exp...
Tags for this Online Resume: Management, Clinical Research, Data Management, Protocol, Research, Assessments, Forth Programing Language, Good Clinical Practices, Monitoring, Training
Clinical Research Associate
The contribute in the successful implementation of new drug trials with particular emphasis on subject safety.
I am a Regisered Nurse with interests and experience in Clinical Regional Monitoring and Clinical Management/Project Manager - 15 Years of Experience - Near 06512
I have a strong clinical background as a Registered Nurse prior to my joining the pharmaceutical industry. This has been beneficial in the course of my career. I have expertise in many areas and observational abilities in tracking subject safety and tolerability. I am aware of site challenges, having conducted clinical trials in large hospital settings as an RN and can be supportive and provide suggestions to sites when ch...
Ideal Companies: DOCs ICON Pfizer
Tags for this Online Resume: Clinical Research, Oncology, Immunology, Neuroscience, CRA, Registered Nurse, Clinical Manager, Data Management, Clinical Oversight, Project Management, CRO, CRO Oversight, GCP, ICH, Pharmaceutical Industry, Clinical Site Management, Compliance, Safety Management, Site Selection, Regulatory Compliance, Continuous Quality Improvement, Medical Writing, FDA Reporting, Trial Master File/eTMF, Cross-Functional Facilitation, Strategic Planning, Risk Analysis, Safety Oversight and Reporting, Data Targeted Review
Experienced Manufacturing and Production Manager, extensive remote experience and Business Education Manager
Solutions focused, innovative management professional with dedicated military service. Effective leader who quickly masters new roles and technologies to achieve positive results. Works extremely well alone or with team members and groups with diverse backgrounds. Capable of handling every assigned task with accuracy and efficiency.
Ideal Companies: Caterpillar, John Deere, Sara Lee, Eaton, Borg Warner, Emerson
Tags for this Online Resume: Scheduling, Billing, Business Development, Human Resources, Management, Manufacturing, Microsoft Outlook, Scheduler, P&L
