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Online Resumes with "GCP "
Senior pharmaceutical scientist with professional experience in drug safety, toxicology, biomarkers and clinical trials
Senior biomedical scientist with 14 years of pharmaceutical industry experience, in both the preclinical and clinical setting, with a focus on discovery and application of biomarkers of safety and efficacy. Served as line function expert on cross-functional project teams as well as extensive experience in leading specialty sub-teams. Excellent analytical, verbal and written communication skills, with extensive experience in...
Tags for this Online Resume: drug safety, biomarkers, clinical research, clinical trials, toxicology, data analysis, scientific writing
Clinical Research - 20 Years of Experience - Near 95050
Clinical trial Research or Pharmacology Research
Tags for this Online Resume: San Francisco, Clinical Trials, Pharmacology, Oncology, Drug Trials, Wet Chemistry, Protocol Compliance, ICH-GCP
Clinical SAS Programming - 4+ Years of Experience - Near 43016
Experienced in SAS/BASE SAS/SQL, Assisted in CRF Annotation and edit check plans, experienced in offline listings, Good working knowledge on SDTM,CDISC Std. Good knowledge on Demography, concamitant medications, Medical History etc..
Tags for this Online Resume: Dublin,Ohio, SAS, BASE SAS, SDTM, CDISC, CLINICAL RESEARCH, ICH-GCP
Manager - 13 Years of Experience - Near 46037
Sr. Manager with 5 years’ experience managing individual contributors and supervisors in a global environment Proven Quality Assurance leadership skills to ensure IT/Lab/Site compliance with internal procedures and regulatory requirements Demonstrated ability to successfully lead continuous improvement initiatives with effective planning and organization skills • Lead CAPA Investigations • Host FDA/CAP/DOH/Client Audits ...
Tags for this Online Resume: CAPA, 21 CFR Part 11, SDLC, Metrics, FDA, Quality, Validation
Quality Assurance Auditor - 12 years Experience - Pharmaceuticals
Quality Assurance Auditor with proficient skills and experiences in various compliance disciplines. Have a passion to conduct local, international, and global audits, training, and provide guidance services within the following regulatory specialties: â?¢Good Laboratory Practices (GLP) 21 CFR Part 58 â?¢Good Clinical Practices (GCP), VICH GL9, Document 85 â?¢Environmental Protection Agency GLP (EPA-GLP), 40 Code of Federa...
Tags for this Online Resume: Auditor, GLP, GCP, Quality Assurance, QA Manager, QA Auditor
Clinical Quality Assurance -13 Years of Experience - Near 92121
Experienced Document Control Associate for the pharmaceutical, device and technology industry working in a GLP, GCP, and cGMP environment. Demonstrated project manager for several document management types, with ability to self-prioritize to meet management and customer demands. Responsible for the successful execution of change control activities for all document types. Effective communicator with strong grammatical, wr...
Tags for this Online Resume: San Diego, CA, GLP, GCP, cGMP, Document Control, Quality Assurance
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
Clinical Research - 1 Years of Experience - Near 56003
To be part of an organization that is thriving on the latest technology, which gives a challenging career, in terms of accomplishing the responsibilities, where I can optimize exposure, vertical and communication skills. Also, to improve myself by continuous learning in and outside the purview of my responsibilities such that I can contribute to the progress of the organization.
Tags for this Online Resume: ADR reporting , ICH GCP, P.V, English Language, Hindi Language, regulatory affairs, protocol writing, article, leaflet, literature writing
Clinical Research - 20 Years of Experience - Near 33498
As the Director of PSRI, I specialize in the analysis and restoration of Complex Multi Therapeutic Clinical Programs with a minimum of Invasive change to the Sponsors Design. I concentrate on complex, Pharmaceutical, Biologic, Medical Device, Vitamin/Supplement and Food Clinical Research. I'm experienced and well versed in all FDA/GCP & ICH requirements for conducting Phase I thru IV research. I have worked on all phase...
Tags for this Online Resume: Documentation, Pharmaceutical, Clinical Operations, ICH, Management, Protocol, Audit, Clinical Research, Good Clinical Practices, Medical
Clinical Research Scientist
My goal is to leverage my strong scientific, medical, and clinical trial experience as the foundation for building a career in Pharmaceuticals and Biotech companies. The positions I am interested are Clinical Scientist, Drug Safety Scientist, PV scientist, Non-MD Study Clinician, Clinical Trial Manager and other opportunities in San Francisco bay area. I am open to both permanent and contract positions.
Tags for this Online Resume: San Franciso, Oncology, Research, Trials, Management, Scientist, Pharmacovigilance, GCP
Medical or Health Services Manager - 4 Years of Experience - Near M1H 3G6
COVER LETTER: Dear Sir/Madam , Please find attached my resume for your consideration for Clinical Research Associate position. I have B.Sc, M.D and Post Graduate Diploma in Clinical Research, Drug Safety and Pharmacovigilance. I have experience in communicating with patients using sound judgment, in order to resolve any problems. I am a logical thinker, capable of following complex procedures quickly and accurately. I have ...
Tags for this Online Resume: Cancer, Cardiopulmonary resuscitation (CPR), Management, Cardiac Cath, Computer Aided Software Engineering, Diabetes Mellitus, Endometriosis, Insulin
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 ...
Tags for this Online Resume: C Programming Language, Cancer, Data Analysis, Data Processing, ELISA, EMT, Extensible Markup Language (XML), Genotyping
