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Online Resumes with "Clinical Trial Studies "
Highly ambitious, motivated personable business individual with excellent communication and organizational skill, providing a professional demeanor gained through extensive interaction through the public for over 14 years. One who excels at multi-tasking in a fast-paced environment, by completing job duties within the appropriate time.
I'd like to look for a job in credit risk analysis and direct marketing research.
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 ...
Clinical Data Coordinator with over 12 years experience and expertise working in a Data Management environment within a clinical research organization. Organized and able to handle multiple clinical trial studies along with excellent problem solving ability.
Objectives: To seek a growth opportunity in US pharmaceutical industry, a role in clinical research areas such as Drug Safety/Pharmacovigilance, Medical Writing, and Medical affairs.
Tags for this Online Resume: drug safety, pharmacovigilance, medical writing, clinical research, clinical trial or study, managerial/supervisory experience, senior level in global pharma company, risk management, US work authorization, GCP, FDA, ICH, detail-oriented, results driven, drug , medical , safety, clinical, writing, FDA, GCP, ICH, senior, regulatory, responsible, pharmaceutical
My objective is to expand in my professional experience, while contributing to your company's overall success.
Registered Nurse Indianapolis, IN Clinical trial study coordinator, IV/Infusion nurse Homecare
With 14 years in remote SAS development and Statistical Programming, I have gained invaluable expertise leading and contributing to summarizations of clinical trial results for pharmaceutical and biotech firms. I have been a “go to” SAS resource for Amgen, Cephalon, BD Medical Systems, Astra-Zeneca, Boehringer-Ingelheim, Smith-Kline & Beecham and Miami/Dade Water and Sewer Administration (WASA). I have successfully led mu...
Obtain a position where I can maximize my BSN, RN nursing, pharmaceutical research and management skills. Apply my knowledge of AE reporting, quality assurance, risk management, auditing, clinical trial studies, regulatory reporting, employee supervision and development, and training experience.
Established this firm to leverage extensive clinical data management experience in supporting clients’ clinical trial laboratories as well as clinical trial data of various therapeutic areas. Working remotely, manages a variety of activities including high-volume clinical double data entry reconciliation and data validation of Phase I, II, and III clinical trial studies. Enhances client value by performing double data entry...
Michelle Straka, BSHS, CPT 1163 Portsmouth Circle Medina, Ohio 44256 Cellular: (216) 337-2007 Home: (330) 722-2165 Email: firstname.lastname@example.org Linkedin account: http://www.linkedin.com/pub/michelle-straka/1b/964/aa2 Objective Obtain the position of Clinical Research Associate to further advance monitoring career. About four years additional experience in research as a study coordinator, regulatory coordina...