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Online Resumes with "Clinical Trial Monitor"
Seasoned Clinical Research Professional with 10+ years experience in Clinical Research, including, CRA, Lead CRA, and Project Management duties. THerapeutic areas include oncology, endocrine/metabolism, and CNS.
Obtain a position that will allow me to utilize my quality organizational skills, communication skills, educational background, and ability to work well with people in a team enviroment.
I desire to continue my work in the field of clinical research, utilizing 12+ years of experience in order to provide services as a home-based salaried or contract clinical trials monitor, eventually transitioning into a Lead CRA or Project Management position
Sr. Scie - over 20 years experience major pharmacutical company - conducting and monitoring GLP clnical trials,
Seeking a position in pharmaceutical industry as a Clinical Trial Monitor In-house, Regional Monitor, Clinical Quality Assurance,Clinical Drug Safety
Seeking a position as a Medical Assistant/Phlebotomist with a goal of providing the highest level of patient care to a health care facility and make significant contribution to th field's continuing growth.
I am looking for a job that will enhance my skills in purchasing, logistics, and human resources. I want the job to enable to for me to learn new skills and tasks and stretch my abilities. I am a jack of all trades and love multi-tasking and learning other jobs while at a company. I believe that is essential to grow with a company and to understand the operation as a whole.
Tags for this Online Resume: Java Script, Microsoft Word, Microsoft Access, Microsoft Powerpoint, Microsoft Exel, Peoplesoft, Kronos, Oracle, Profit and Loss Statement, OSHA, Sarbanes Oxley, JD Edwards, EZ Buy, Negotiator, Purchasing, logistics, supply, Customer Service, Planner, Microsoft Outlook, Operations Management, Human Resources
Clinical Trial Monitor/Manager - 6.4 yrs experience in Clinical Trial monitoring.management. Therapeutic expertise: Oncology. Others: GI, Resperitory, CVS, Nephrology, Endocrinology.
My Career Objective: To contribute my best of knowledge and skills in the field of Clinical Research to an excelling Pharma/CRO company which conducts quality and ethical clinical trial as per GCP guidelines. Also to bring profit to the company in drug development & pahrmaceutical market by timely delivery of quality work. I also strive to enhance my knowledge and skills and excel in career at all level.
Interested in continuing in the research science field as a clinical trial monitor or as a research scientist.
Looking for possible home based consultant opportunities – in clinical trial monitoring or management
Sr Medical Writer with 14 year experience - Mississauga, Ontario