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Online Resumes with "ICH"
Professor of German, English, & Film
Wenn Sie einen guten Deutschprofessor wollen, bin ich derjenige.
Aircraft Rigging Assembler
Clinical Research Associate-8 years experience
I'm an ambitiuos Clinical Research Professional contributing 8 years to the industry in project management, quality assurance/quality control, site coordination, internal clinical monitoring, and data collection. My healthcare background has rewarded me with skills in mulitiple thereapeutic areas consisting of: practice management, patient care, records system development, and team leadership.
Tags for this Online Resume: Houston, Pharmaceutical, ICH-GCP, HIPAA, FDA, Quality Assurance/Quality Control, Monitoring, Clinical Research
Pharmaceutical Research Scientist, Regulatory/Quality/Project Manager/.EHS/Safety, York, PA
To achieve career growth and opportunity by transitioning from phamaceutical product development scientist (19 years experience) to EHS/Safety field (8 years direct experience), project management, or quality managment.
Ideal Companies: GSK, Amazon, Airgas, Astrazenaca
Tags for this Online Resume: research scientist, GMP, Safety/EHS, Quality Management, Project Management, QbD, FDA, Pharmaceutcial Product Development, Risk Assessment, DOT, EPA, OSHA
Clinical Research Associate
To obtain a Clinical Research Position in the Minnesota Area.
Tags for this Online Resume: Knowledge of 21 CFR, Quality System Regulation (QSR), Medical Device Reporting, Regulatory Compliance , Regulatory Submissions , ICH GCP Guidelines
Med Tech 18 years MBA Health Mgmt.MS Project mgmt, CRA enrolled cert.
I am looking for an opportunity in Clinical Resaerch. Willing to start in entry level position however, I am experienced in laboratory management, FDA, osha, ICH and other regulations and protocols.
Tags for this Online Resume: clinical research, project coordinator, medical technologist, Atlanta, Pharmaceutical , trial coordinator
Clinical Pharmacovigilance/Drug Safety
Tags for this Online Resume: MD, ARISg, FDA & ICH guidelines, MedDRA, WHO-DD, iMedidata & RAVE
Biostatistician-6 years’ experience- SAS -SPSS - ICH & EMEA guidelines - Project Statistician -GSK/ICON/Freelancer
I'm a Biostatistician with Master's in Statistics and have over 6 years of experience in Clinical Research Domain. Expertise in writing Study report analysis plan, Statistical analysis (Generating Tables, listings and Graphs) using SAS and review of Clinical report and manuscript.
Quality Assurance Engineer
I am a Senior Quality Assurance Engineer with 20 years experience in the consumer good and food technology industries. I have expertise in QA, FDA and ICH/ISO compliance, R&D and manufacturing supply chain experience. I am a six sigma black belt equivalent(internal company training)
Senior Clinical Operations Supervisor - 11 years experience - GCP-ICH
Drug Safety Physician, Medical Monitor, 11 years experience
An accomplished individual offering long-term experience in the pharmaceutical industry. My areas of expertise include Medical Affairs, Drug Safety, Medical Monitoring, and Clinical Research Associate. Additionally, I possess 18-year medical practice including head and neck Oncology.
Tags for this Online Resume: Medical Monitor, PSUR, GCP/ICH, CRA, Remote, MedDRA coding, Adverse Events, Risk Management Plan, SMQ
Document Specialist - 20 years experience - Philadelphia
Tags for this Online Resume: eCTD, IND, submission readiness, NDA, Document management , ICH, FDA, EMEA, SOP
