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Online Resumes with "Clinical Trial Studies "
Experienced, Professional and Reliable Office Administrator
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.
Ideal Companies: The Hour Magazine, Essence, E-Entertainement, Karmanos Cancer Institute, Lifetime Adoption, Lifetime Womens Network, Beaumont Health Center, O Magazine, CNN, Sirius Satellite
Manager of Credit Policy and Risk, Marketing Portfolio Analysis
I'd like to look for a job in credit risk analysis and direct marketing research.
Ideal Companies: Discover, Citi
Tags for this Online Resume: Risk Managemnet, Direct Marketing, Marketing Research, Credit Risk, Credit Policy and Risk
Clinical Research Coordinator or Monitor
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 ...
Tags for this Online Resume: CRC, Phase II, Registered Nurse, CRA, Clinical Research Associate, Clinical Trials
Clinical Data Coordinator
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.
Tags for this Online Resume: clinical data coordinator, clinical trial associate, clinical data associates
drug safety/pharmacovgilance/medical writing-9 years experience-global pharmaceutical
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
Collections Agent
My objective is to expand in my professional experience, while contributing to your company's overall success.
Ideal Companies: NIKE, APPLE, COCA-COLA, PEPSI, COACH, ETC.
Tags for this Online Resume: ACCOUNT MANAGEMENT, CUSTOMER SERVICE, BUSINESS DEVELOPMENT
transition into clinical research from RN
Registered Nurse Indianapolis, IN Clinical trial study coordinator, IV/Infusion nurse Homecare
Clinical trials Study Coordinator
Sr SAS Programmer
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...
Manager Pharmacovigilance Quality Systems, Training and Standards
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.
Clinical Data Associate/Manager - six years plus 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...
Clinical Trials Associate
Michelle Straka, BSHS, CPT 1163 Portsmouth Circle Medina, Ohio 44256 Cellular: (216) 337-2007 Home: (330) 722-2165 Email: dodgestealthrt1994@yahoo.com 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...
