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Online Resumes with "ICH guidelines"
Clinical Research Associate
I am seeking a career as a Clinical Research Associate where I can maximize my education and experience. My professional goal is to provide technical, educational support to doctors, nurse specialist and upper management in the direction of improving patient health. I possess technical understanding with ability to perform without supervision and learn as objectives are completed.
Tags for this Online Resume: Knowledge of US federal regulations, ICH Guidelines and GCP., Excellent analytical skills with the ability to interpret clinical data., I have trained and assisted doctors and hospital staff., Strong communication skills (verbal/written/presentation). , The ability to concentrate on detail and work independently. , Advance Cardiac Pacing approved by American of Critical Care Nurse, Clinical, analytical , communication skills
Experienced CRA
Experienced Certified Clinical Research Professional and Certified Critical Care Nurse with excellent communication skills and proven track record of accomplishment in assisting potential and established investigative sites to meet and or exceed established goals. Recognition Awards for communication and cooperation with Co-workers and Sr. Project Management. Excellent knowledge of FDA CFR, GCP/GMP, ICH guidelines. Highly ...
Tags for this Online Resume: CRA, Clinical, Project, Research
Senior Clinical Research Associate
Continue my service, as an educator and monitor in clinical trials for product development with major pharma/device company.
Tags for this Online Resume: Clinical Research Associate, GCP/ICH Guidelines, Bachelor Degree, Clinical Research Coordinator, ACLS Certification, Registered Nurse
Clinical Research Associate
SUMMARY OF QUALIFICATIONS • Foreign graduate Medical Doctor and licensed RN with more than 22 years of clinical and research experience. US citizen. Fluent in English, Russian and Romanian • Extensive training in Good Clinical Practices, ICH Guidelines, SOPs through various Sponsors • In depth therapeutic and protocol knowledge as per Sponsor’s assignment. Excellent organizational and problem-solving skills.
Ideal Companies: Biotech companies
Tags for this Online Resume: research associate, biotech, CRA, Las Vegas, pharmaceutical, health
Clinical Trial Professional
Detailed oriented Clinical Research Professional with medical education background and several publications. Extensive experience working on complex clinical trials in a critical care, cardiology and podiatry environment. Solid knowledge of GCP/ICH guidelines and FDA regulations. Well versed in medical terminology and medical procedures. Possess excellent communication and presentation skills.
Tags for this Online Resume: Clinical Research , Clinical Research Associate, Drug Safety Associate, Clinical Trial Associate, Research Scientist
Research (Clinical or Pharma), North Carolina
Results-oriented individual with clinical and drug-discovery/development research experience. Demonstrated excellent interpersonal and organizational skills with great attention to detail. Recognized as an effective and motivational team player with a consistent track record in meeting multiple deadlines for concurrent projects. Well versed in ICH Guidelines and GCP and the clinical trial process. Able to establish rappor...
Quality Assurance Specialist, Clinical Quality Assurance - 17 years of experience- SQA Active Member
Based on my extensive experience in a variety of Health care and Clinical Research companies, I am confident that I would be a great asset to any organization. My expertise includes quality review of documents, processes and systems, root cause analysis, and CAPA investigation. In addition, my projects have focused on the development of the internal/external audits and risk assessments, audits of final clinical reports, po...
Tags for this Online Resume: Quality Assurance, Clinical Research, Pharmaceutical, Blood Banking, GCP, ICH
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.
