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Online Resumes with "Clinical Trial Assistant"

Clinical Trials Assistant, RTP

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.

Clinical Pharmacovigilance/Drug Safety

Tags for this Online Resume: Clinical Research Assistant, Clinical Trial Assistant, Executive Administrative Assistant, Database Data Entry, Documentation Specialist, Records Management/Archiving

Clinical Trial Assistant

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.

Tags for this Online Resume: clinical trials assistant, clinical research coordinator, clinical research assistant, research assistant, clinical research, clinical project assistant

Clinical Study Associate- study start up, maintenance and close out activities

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.

Tags for this Online Resume: In-house Monitoring, Study Start-up, Clinical Trials Assistant, Clinical Support , Clerical Support , Auditor

Clinical trial assistant

Work with the research team and assist with all aspects of clinical trials

Clinical Trials Associate

Michelle Straka, BSHS, CPT 1163 Portsmouth Circle Medina, Ohio 44256 Cellular: (216) 337-2007 Home: (330) 722-2165 Email: Linkedin account: 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...

Masters Degree Clinical Research Management, current Clinical Research Assistant, Fort Worth

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.

Tags for this Online Resume: Biology, Managment, Clinical Research

Clinical Research Associate

 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...

Ideal Companies: Alcon, Merck, Wythe, Pfizer, Bristol-Meyers Squibb, Covance

Tags for this Online Resume: in-house monitor, Clinical Research Associate

clinical research coordinator, new york

Currently seeking a position as a clinical trials assistant.

Tags for this Online Resume: clinical, clinical trials, pro, clinical research, project coordinator, research, coordinator, research coordinator

Accounting Clerk

Tags for this Online Resume: Clinical Trial Assistant, Project Assistant, Administrative Assistant, Clinical Trial Coordinator

Associate Logistics Coordinator 6 years of experiencia pharmaceutical industry

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 ...

Trial Master File/Document Quality Coordinator

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 ...

Tags for this Online Resume: trial master file, clinical assistant, data enty, filing