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Online Resumes with "Informed Consent"
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.
I have completed a Masters program in Biotechnology. I have keen interest in Clinical Research and Regulatory Affairs. I am looking for an entry level Clinical or Regulatory position. I have research site coordination experience in the areas of Rheumatology and Pain research. I am also ICH and GCP certified.
Tags for this Online Resume: CRF writing, patient follow up, administering informed consent form, administering psycometric scales, source documents review, Reporting SAE’s, Pre-screening and recruiting patients, -Submitted documents to the Ethics Committee, Rheumatology, Pain
I am very enthusiastic about beginning a career in clinical research. As you can see I have no direct experience in this field, however, my father was in a clinical trial study at Emory University for his prostrate cancer. I followed his participation in the study and was involved in his care during this time. In addition, as a home health care nurse, I treated several patients that were also involved in clinical trials in ...
Passionate, hard-working, intelligent, leader, compassionate, organized
Ideal Companies: I would enjoy working with any CRO or Sponsor who values and rewards excellence and a strong work ethic from their employees.
not only exceptional technical competency but also superior analysis, problem-solving abilities, leadership, communication and team member experience.
Ideal Companies: Companies that have more than 50 employees and been in business for awhile.
Can undertake most of the tasks and works independently. Very much focussed on the timelines and quite goal tending. Willing to help others in their prioritized tasks. Excellent planning, design and implementation. Highly experienced in writing reports and data analyses.
Seeking a full-time position utilizing my written,organization skills in a government, health care, clinical research setting with an emphasis on regulatory affairs submissions, informed consent, and FDA requirements
My objective is to support all health professionals in understand clinical research from the correct methodology to data collection to data analysis. Can support in writing case report form, questionnaire design,inform consent form
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...
Looking to work for a company that has growth potential. Want to move into management. Company that has good 401K. Company that allows the employees to come to managment with problems or suggestions.
Tags for this Online Resume: Document Specialist(paper & electronic), Clinical Research Associate II, Master File & Investigator File Specialist, Informed Consent Reviewer, Remote Site Management, Investigator Meeting Speaker
I am an excellent candidate for a Clinical Research Associate position due to my unique combination of experience in Preclinical Research and Development, Pharmaceutical Sales, and CRA Training. In addition to the skills and accomplishments detailed in my c.v., please consider the following highlights: Certification from Barnett International (July 2012): 10-Week CRA & CRC Beginner Program. Coursework emphasized FDA reg...