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Online Resumes with "Clinical Trial Assistant"
Diligent, accurate and reliable Clinical professional with a reputation for completing high quality, complex diagnostic lab procedures in a timely fashion and in accordance with SOP’s, ICH guidelines and OSHA standards. Eager to learn all broad aspects involving Clinical Research & Development and all scientific and administrartive approaches it entitles.
To obtain a position in the field of clinical research, to apply the knowledge I have learned through my coursework, and to gain additional knowledge of the field through hands-on experience.
Office support professional experienced in fast-paced environments demanding strong organizational skills, technical and interpersonal skills. Trustworthy, ethical, and discreet, committed to superior customer service. Confident and poised interactions with individuals at all levels.
Work with the research team and assist with all aspects of clinical trials
Michelle Straka, BSHS, CPT 1163 Portsmouth Circle Medina, Ohio 44256 Cellular: (216) 337-2007 Home: (330) 722-2165 Email: email@example.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...
I received my Bachelors Degree in Biology and my Masters Degree in Clinical Research Management. I am currently working as a Clinical Trials Assistant for a pharmaceutical company, but am looking for career growth, such as a Clinical Research Associate positions or other related occupations in Clinical Research.
John is detail oriented, highly dependable previous site monitor and study coordinator with 4 years and 6 months experience, including assistant project management in the pharmaceutical development industry He has attained knowledge and experience in 4 years of hands on provision of care for elderly and disabled persons assisting them with activities of independent daily living as well as dealing with transitional aspec...
Currently seeking a position as a clinical trials assistant.
Natalia is a Biologist by profession; she graduated from Pontificia Universidad Javeriana in 2008 and her experience starts in 2007 where she did her practice in Brazil at Pontificia Universidad Catolica de Minas Gerais. In 2008 she joined Merck Sharp & Dohme and worked in Clinical trials as Assistant Data Coordinator, in 2011 she was promoted to Pharmacovigilance as Associate Data coordinator until 2012. Natalia Gómez is ...
I am a Document Quality Coordinator/Clinical Trial Assistant with 3 years experience with pharmaceuticals and 3 years with CROs. My expertise in with organizing, maintaining, and quaity checking Investigator files and General files, hard copies and electronic documentation. I keep track of updates on essential documents from sites - IRB approvals, CVs, Medical licenses, and Financial disclosures,protocol, IB, study manual ...