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Online Resumes with "Clinical Trial Process"
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
A tree that branches out and continues to grow.
Ideal Companies: Government, Health Care Insurance Co., Pharmacy, General Electric
Tags for this Online Resume: Customer Service, Customer Service Supervisor, Data Entry, Billing
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
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...
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...
Senior Research Nurse Coordinator
I'm a competent, organized, detailed oriented and efficient Clinical Research Nurse Professional with 10 years experience and proven administrative skills. Experience includes OB/GYN, Vascular Surgery, Podiatric and Ophthalmology Reserach. Excellent communication skills and proficient in time management and problem solving abilities. Knowledge of GCP and ICH guidelines, regulatory requirements, and the clinical trial process.
Senior Lead Clinical Research Associate - MPH CCRA - Certified - Southeast Contract CRA / LCRA
To provide an insightful, knowledge driven assessment of the clinical trial process or onsite monitoring to advance the progress of the trial and/or the team as a whole.
Pharmaceutical Deputy Compliance/Internal Auditor/Governance/Risk Management/Internal Controls/Change Management
I am interested in a position where I can leverage the skills and experience I have gained over a career in the pharmaceutical industry.I am a skilled professional with over 15 years experience in compliance, risk management, corporate governance and change management, as well as R&D internal audit and assurance. I am an excellent communicator, with well-developed speaking and writing skills and in-depth subject matter e...
Ideal Companies: Shire Pharmaceuticals, Novo Nordisk, Pfizer, AstraZeneca, Endo, Sanofi
Tags for this Online Resume: Internal audit, Training, Risk Management, Governance, Internal Control, Change Management, Risk Assessment, Facilitation, External Benchmarking, Communication through writing, Thought Leader, Team Player, Project Leader, Business Liaison, Contract Analyst, Assurance, Risk Profiles, Compliance
Clinical Research Associate - Entry level - Waterloo
Driven, dynamic, and detail oriented. Trained in ICH/GCP guidelines to monitor clinical trial processes. Actively seeking an entry level CRA position within clinical trial programs.
Tags for this Online Resume: ICH/GCP, Clinical Research, SOPs, Case Report Forms, Microsoft Office Suite, Phases I - IV trials, Recruitment
Medical or Health Services Manager - 10 Years of Experience
Career Summary Pharmacist by education, with 10 years of Industrial Experience in various domains of Preclinical and Clinical Research and Development as well as IMP Supply Chain Management. R&D Professional with 4 years of Clinical Research experience from within the CRO as well as Sponsor environment that includes PK/PD studies, Phase II, III and IV studies and more than 1 year of experience in Preclinical research labora...
Tags for this Online Resume: Clinical Research, Clinical Supply , Trial Management , Microsoft, Microsoft Excel, Microsoft Office, Microsoft Word, Microsoft Word, Clinical Research, Management, Research, Analytical Skills, Audit, Cardiovascular, Compliance, ENT
Clinical Trial Assistant, Downingtown
Support Clinical Trials in processing documents from study start-up to study close out.
Tags for this Online Resume: clinical , support, assistant, research, project, study
Clinical Research - 15 Years of Experience
SUMMARY A highly experienced Clinical Research professional with considerable experience in all stages of clinical trial processes, gained within the Biotech, CRO and Pharmaceutical environments. Key experiences areas: CNS- Psychiatric/Migraine/Alzheimer/Seizure/Movement Disorders Epilepsy, Cardiovascular- Statins, Type 1 & 2 Diabetes, Infectious Disease- HIV, AIDS, Autoimmune (NMO), Medical Device-stents, valves, glucomete...
Tags for this Online Resume: Clinical Programs, Clinical Research, Research, Protocol, Cardiovascular, Management, COPD, Distribution, Oncology, Vendor Management
