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Online Resumes with "GCP ICH"
Biochemist - 18 Years of Experience - Near 84037
Compliance and Quality Manager in Pharmaceutical manufacturing. Highly experienced with Aseptic, Solid Dosage, and Liquid Manufacturing including 15+ years in management. Key player in successful Regulatory relationships with Inspectors across 4 continents. Developed and implemented Quality systems, processes, procedures, and policies. People acumen across all levels from executives to entry-level.
Tags for this Online Resume: Quality, Compliance, Quality System, Standards (GMP, GLP, GCP, ICH, ISO, WHO, CE, Med Device), Training, Investigations (CAPA), Documentation, Salt Lake City
Featured Profile
Clinical Research - 6 Years of Experience - Near 92649
Experienced Clinical Research Professional interested in positions within the pharmaceutical or medical device industry.
Ideal Companies: inventiv, johnson & johnson, covance, covidien, peregrine
Tags for this Online Resume:
Irvine, CCRP, regulatory affairs, clinical project manager, EDC, budgets , timelines, contracts and budgets
Senior Clinical Trial Manager - 10 year experience - GCP/ICH - Mentor/Trainer
My goal is to obtain a position as a clinical manager or line manager. I have an additional 16 years of experience in leadership and management with the military as enlisted and an officer.
Tags for this Online Resume:
Senior Clinical Trial Manager, Clinical Project Manager, Manager of Clinical Operations, GCP, ICH, FDA
Biologist - 5 Years of Experience - Near 60608
Summary * 10 years research experience, broad scientific knowledge with solid publications. Lead projects from initiation, planning, design, and execution to publication * Daily responsibility in optimizing conditions, developing protocols and training graduate students * Strong R programming skill, familiar with statistical inference and regression modeling * Familiar with bowtie2, tophat, cufflink, samtools and rMats for ...
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C Programming Language, Cancer, Data Analysis, Data Processing, ELISA, EMT, Extensible Markup Language (XML), Genotyping
Clinical Research - 6 Years of Experience - Near 75287
PROFESSIONAL SUMMARY: A CRA with strong eye for detail and exceptional ability to interpret and follow instructions Possesses the ability to collect accurate data in line with client specifications excellent analytical and organizational skills knowledgeable in FDA regulations, GCP/ICH guidelines, seeking to join an organization that makes research subjects' safety its first priority. CORE QUALIFICATIONS: * Over 5 years exp...
Tags for this Online Resume:
Management, Clinical Research, Data Management, Protocol, Research, Assessments, Forth Programing Language, Good Clinical Practices, Monitoring, Training
Clinical Research - 1 Years of Experience - Near 27704
A goal-driven dependable and dedicated management professional with over 12 years' solid experience in Clinical Data Management operations at a non-profit organization. Has extensive knowledge of GCP ICH and FDA regulatory requirements regarding management of clinical trials data. Expertise in data management practices for paper studies as well as electronic data capture systems. Has a proven ability to effectively communic...
Tags for this Online Resume:
Data Management, Email, Management, Query, Training, Documentation, Clinical Research, Compliance, Data Entry, Project Management
Clinical Research Associate
SUMMARY: To apply my knowledge of FDA Good Clinical Practice guidelines/ICH guidelines, extensive site/field Clinical Director, Site Lead Study Management, in addition to my experience with various therapeutic areas of medicine, to a position as a Clinical Research Associate. AREAS OF EXPERTISE * Management * Interview candidates and either make a selection decision or recommend individuals for hire. * Able to manage multip...
Tags for this Online Resume:
Clinical Research, Research, Accounting, Acquired Immune Deficiency Syndrome (AIDS), Advertising, Amazon Elastic MapReduce, Audit, Basic First Aid, BLS, Budgeting
Clinical Research
Summary of Qualifications Clinical Research Manager, Associate, Monitor, Coordinator, with over 25 years experience in the medical field and 21 years experience in clinical trials with extensive experience in the fields of Cardiology, Electrophysiology, Neurology, Urology, Autoimmune, Respiratory, Gastroenterology, Weight Loss, Diabetes, Women's Studies, Arthritis, COPD, Gynecology, Endocrinology, Rheumatology and Stem Cell...
Tags for this Online Resume:
Monitoring, Protocol, Cardiovascular, Clinical Research, Management, Pharmaceutical, Research, Therapy, Audit, Data Management, Medical Device, CRA, CTM, Clinical Trials
Sr. Clinical Research Coordinator - 14 years Experience -Miami
FMG with 14 years experience working in Clinical Research field from Phase I to Phase IV in multiple therapeutic Areas with vast knowledge of GCP-ICH, Medical Terminology and Regulatory Compliance,Bilingual,Works without supervision or a Team, Detailed and Organized, resolution skills looking forward to join a Pharmaceutical Company to represent it in FL in which my skills can help to enhance the Company Efficacy and Effect...
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Miami, Florida, Sr. CRC, CRA Entry Level, Study Start Up Specialist, Regulatory Affairs
Chief Operations Officer - 11 Years of Experience - Near 92122
SUMMARY of QUALIFICATIONS Available for remote project management and San Diego based roles leading business, clinical, compliance structures. Clinical and regulatory catalyst establishing organizational, technological and scientific intelligence, strategies and resources to ensure a profit based business and marketing environment. * Synergistic Scientific and Business acumen, proficient analytical, technical and interpreti...
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IVD/Medical Device, Pharmaceutical Research, RNA/DNA, Clinical Research, Operations, IND, Regulatory, Project Management, Oncology, AI, cNLP, Genomics
Clinical Project Manager-6 years-France
I supervised the development of several clinical projects in different therapeutics areas and in different countries (France, England, Italy, USA and Canada). I coordinated the clinical activities in respect with the budget, timeframe and regulations (SOPs, FDA-GCP and ICH guidelines). I trained CRAs, site investigators and CROs to ensure study protocol comprehension and compliance (initiation visits, co-monitoring). I plan...
Tags for this Online Resume:
clinical project, oncology, dermatology, cardiology
Clinical Research - 6 Years of Experience - Near 92649
Experienced Clinical Research Professional interested in positions within the pharmaceutical or medical device industry.
Ideal Companies: inventiv, johnson & johnson, covance, covidien, peregrine
Tags for this Online Resume: Irvine, CCRP, regulatory affairs, clinical project manager, EDC, budgets , timelines, contracts and budgets
