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Online Resumes with "Drug Safety Associate "
I am seeking for a stable and well established company that is growing. Also,what I am looking for in a new job is for employers that care about their employees and acknowleges them for their good hard work. I would also hope that good training is provided so that the individual such as myself can be productive for the company and contribute towards it's success rate. I would also hope that it was a warm welcoming environm...
Detailed oriented Clinical Research Professional with medical education background and several publications. Extensive experience working on complex clinical trials in a critical care, cardiology and podiatry environment. Solid knowledge of GCP/ICH guidelines and FDA regulations. Well versed in medical terminology and medical procedures. Possess excellent communication and presentation skills.
Medical Technologist/Regulatory Affairs Professional with 7 clinical research and laboratory science years experience and extensive knowledge of cGMP, FDA regulations, CAP/CLIA, SOP preparations and editing, clinical research project management.
Seeking a position within an esteemed organization where my expertise would add great value.
An experienced drug safety professional well versed in all aspects of pharmacovigilance including a comprehensive understanding of Safety’s SOPs, Work Instructions (WI), guidance documents and directives associated with safety management, reporting and pharmacovigilance. Experience working in a high-paced GMP environment. Highly motivated and dedicated team player with a passion for continuous improvement.
More challenging position
To work for an organization where I can apply the best of my knowledge and applied experience in Pharmacology which would contribute to the growth of the company & Institution.
To acquire a position as a Clinical Research coordinator in a pharmaceutical company or a CRO that will benefit from my skills, knowledge, experience and enthusiasm and that will give me an opportunity to learn and grow further. To be responsible for the administration, initiation and monitoring of the Clinical research project in accordance with the FDA regulations and ICH-GCP guidelines.
Health care professional with 4 years of experience in development & delivery of health care systems. Combines strong clinical documentation improvement, coding, billing, project, operations, research, business & financial management expertise with more than 2 years of clinical experience as a medical doctor.
Tags for this Online Resume: Healthcare administration, Pharmaceutical, research, Analyst, Leadership, Management, Clinical research, Healthcare Analyst, Healthcare administrator, Drug Safety Associate, Administrator, Manager