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Online Resumes with "Protocol Amendment"
Administrative Assistant
Ideal Companies: Pharmaceutical
Tags for this Online Resume: Administrative Assistant
Have the experience and the knowledge of the clinical trial processes (start-up through close-out), including FDA regulations
Social/Clinical Trials Research Assistant/Coordinator/Clinical Support Specialist
Tags for this Online Resume: ICH Guidelines, IND Application, Guidance on HIPAA Privacy in Research, Protocol Amendment, Quality Assurance (QA), Serious Adverse Events (SAE) or Serious Adverse Drug Reaction (serious ADR), Source Document, Randomization
Senior Technical Editor, Electronic Document Coordinator/Specialist
Enthusiastic New Graduate
Offering: Practical experience and education in social science research, effective communication and demonstrated diligence, interest in healthcare and human services. Long term goal is a graduate degree in health education and promotion.
Tags for this Online Resume: research assistant, case manager, psychology, non-profit
Registered Nurse, Clinical Research Coordinator, pharmaceutical trials, consultant, experienced
As my career goals are on target with my education and expertise, I am now seeking a non-traditional nursing role where my experience and education have provided me with knowledge in a wide range of areas with many prospects that require skills I have acquired over a long career. I am ready to move in a new direction using my passion for research, law, creativity, travel, information technology, consulting, advising and the...
Ideal Companies: Stanford, Amgen
Tags for this Online Resume: Registered Nurse, Research, Medical Records Reviewer, BSN, Coordinator , Consultant, Sales, Entrepreneur, Clinical Research Coordinator
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...
Clinical Pharmacovigilance/Drug Safety - 10 Years of Experience - Near 19440
Summary Clinical Scientist/Clinical Data Analyst/Clinical Data Management/Project Coordinator/GLP auditor/Research Biologist with over 15 years experience in the pharmaceutical industry. Authored/QC review of protocols, protocol amendments, protocol clarification letters, informed consent forms, risk language, periodic safety reports (PSUR, DSUR, QSR), investigator brochures, medical monitoring plans, clinical SAE narrative...
Tags for this Online Resume:
Protocol, Oncology, Audit, Monitoring, Critical Care - Neurology, ICH, Neurology, Quality Assurance, Test, Data Quality
Contract Medical Writer
Summary Work Experience: Strong background in medical writing and biotechnology product and services development, with a solid publication record in the peer-reviewed medical literature in addition to biotechnology analyst articles-an unusual combination of medical writing expertise, analytical skills, data analysis, management experience, and medical knowledge. Participate in pre-clinical, clinical, and commercial research...
Tags for this Online Resume:
Business Development, Cancer, Clinical Research, Medical Writer, regulatory science, biologics, drugs, medical device
Featured Profile
Clinical Research Project Manager Interested in Growing with a Patient Centered Organization
My career goal is to first obtain a clinical research project manager position with an innovative, patient-centered pharmaceutical company, medical device company, clinical research organization (CRO), or medical center. Eventually, I would like to prepare to segue into international development as a Senior Director and play an integral role in developing a research infrastructure for new companies and/or those interested ...
Ideal Companies: Pfizer, AstraZeneca, Becton Dickinson, etc.
Clinical Research Project Manager Interested in Growing with a Patient Centered Organization
My career goal is to first obtain a clinical research project manager position with an innovative, patient-centered pharmaceutical company, medical device company, clinical research organization (CRO), or medical center. Eventually, I would like to prepare to segue into international development as a Senior Director and play an integral role in developing a research infrastructure for new companies and/or those interested ...
Ideal Companies: Pfizer, AstraZeneca, Becton Dickinson, etc.
