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Online Resumes with "Clinical Research Associate"
To manage clinical trials for both pharmaceutical and biotechnical companies.
A job! Been laid off since january and would like an in house position with a pharma or device company within a 50 mile radius of 95404
My focus is administrative management. Currently I am looking to enhance my job opportunities by exploring other career options; applicable to my skills and education. I have spent many years working within clinical research settings for both pharmaceutical and medical device organizations. In order to realize my potential, I am willing to think outside of the box.
Clinical Research Associate or Epidemiologist
I am currently looking for an appropriate job opening in a Research Institute. I have five years experience as a Clinical Research Associate (as Regulatory Officer and Medical Writer). I had been working with reputed pharmaceutical companies in India. I have led a team of Medical writers and as a part of them, I have written Clinical and Pre-clinical overviews on more than 100 molecules for regulatory dossier submission ...
Senior Clinical Research Associate-30years experience in monitoring pysicians participating in clinical research
Senior Clinical Research Associate
Profile: Certified Clinical Research Associate professional with extensive recent focus in CVS research and clinical trials. Combine resourcefulness and problem solving skills with clinical knowledge to consistently deliver improved research and production results. Team player dedicated to quality, continuous improvement and bottom-line objectives. QUALIFICATION HIGHLIGHTS • Knowledgeable in all areas of research including...
I wish to be a Clinical Research Associate. I am pursuing my Masters in Pharmacology and Toxicology and will graduate by August 2010. So also, I am a MD from India practising General Surgery since 8 years.My strong clinical background would complement my research capabilities and prove invaluable in this position as a Clinical Research Associate at your organization.
Monitor clinical trials
To work with a professional organization in which I can use my nursing experience to collect data,enter data and patient case history reports ,assist in case studies,assist in setting up sites,reviewing records in house or in the field.
My career goal is to have an impact on the entire process of clinical studies. I would like to broaden my horizons beyond the normal CRA role performed and be involved in the entire clinical study from start to finish. I want to be involved in the protocol from beginning (developing the protocol) to the FDA submission. From my previous experiences I know I can have a positive effect on the successful outcome of studies.