CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "GCP "

Chemist - 11 Years of Experience - Near 75002

To provide my expertise for companies in need of support with R&D, quality control and regulatory. * Qualities Highly detailed and dedicated person, fast learner strong leadership skills proven orga - nizational and management skills and self - motivated. A team player and performs well under pressure. Fields of experience include but are not limited to Microsoft Office Word, Power Point and Excel, SharePoint, Visio, Adobe ...

Tags for this Online Resume: Audit, Medical, Regulatory Affairs, Complaints, Product Development, Chemistry, Market Research, MSDS, Research, sas, oncology, phase, gcp, 6 sigma, SOP, R&D, Cosmetics, Drugs, FDA, QC

Clinical Research - 16 Years of Experience - Near 07052

SUMMARY: Clinical research professional with experience conducting and managing sponsor related clinical trials Phases I-IV following GCP and ICH requirements and guidelines. Clinical trial experience in various indications including Oncology (Solid Tumors, Prostate, Lymphoma and Renal Cell Carcinoma) and Cardiovascular (myocardial infarction, acute ischemic stroke, and Venous Thrombo-Embolism). Strong team player experienc...

Tags for this Online Resume: Management, Billing, Direct Patient Care, Integrate, Inventory, Inventory management, Medical, Medical Billing

Animal Scientist - 1 Years of Experience - Near 70820

It is hard to summarize my background experiences in few lines, but what it matters the most that I am so capable to take any methodology conception to completion. I am interested in finding a job that is a good fit for me and there is room to contribute and grow in a team-oriented environment.

Tags for this Online Resume: ELISA, Research, Manufacturing, Quantify, Statistical Analysis, C++ Programming Language, Chemistry, Cobol Programming Language, D.O.T., Electrophoresis, pharmaceutical, sas, protocol, gcp

Clinical Research

SUMMARY Accomplished individual with strong background in understanding complex relationships between critical organizational elements well enough to unlock great organizational performance. Outstanding communication with proven ability to build and lead highly efficient teams, to train technical personnel and to convey complex concepts in understandable terms. Skilled in multiple areas of technology, including advanced Mic...

Tags for this Online Resume: Quick Books, Quickbooks, Accounting, Accounting Functions, ATX (Network Provider), Customer Relationship Management, Microsoft Access, Software, Software Development, Accounting Software, clinical, protocol, ich, trial, gcp, phase, pharmaceutical

Clinical Research - 7 Years of Experience - Near 60640

SUMMARY OF QUALIFICATIONS: My experience includes working for PAREXEL International for over seven years, following two years in pediatric neurological clinical research of Boston Children's Hospital. My recent experience includes Software Validation and assisting in project management as well as being directly trained on ClinPhone 4 at the PAREXEL office in Crawley, UK. My accomplishments in the role of Principal Software ...

Tags for this Online Resume: Services, Software, Management, Software Development, Clinical Research, Critical Care - Neurology, Magnetic Resonance Imaging (MRI), Microsoft Windows, MRI, Neurology, IRT, IxRS, randomization, trial supply management, testing, process improvement, SME, ePRO, validation, quality assurance, study management, trial management, software development lifecycle, patient management, subject management, subject, trial, clinical, phase, gcp, protocol, pharmaceutical

Certified Clinical Research Coordinator - 13 Years of Experience - Near 34202

Seasoned Certified Clinical Research Coordinator with 13 years' experience as a CRC, including experience in marketing, advertising, and regulatory document completion and submission. Completed my duties with great attention to detail, compassion, professionalism, confidentiality, and care. Seeking a position in healthcare/clinical research/pharmaceutical industry that will allow me to continue to exercise these skills and ...

Tags for this Online Resume: Clinical Research, Research, Good Clinical Practices, Protocol, Advertising, Documentation, Marketing Management, NPI, Training, Accounts Payable, clinical, trial, phase, gcp, protocol, pharmaceutical, GCP, IRB, CRF, ich, AE, SAE, SUSAR, Inclusion and Exclusion Criteria, ECG, Biological, PK, PG, Substudy, ICF, EDC, Rater, concomitant medications, IP, IP accountability, regulatory documents, master file

Chemist - 3 Years of Experience - Pharmaceutical company in India.

Actively looking for pharmaceutial quality control and quality assurance jobs.

Tags for this Online Resume: Compliance, Certified Protection Professional, Documentation, Electronic Mail, Good Laboratory Practices, High Performance Liquid Chromatography (HPLC), Management, Microsoft, gcp, sas, pharmaceutical, protocol, GDP, SOP

Biostatatician - 18 Years of Experience - Near 07059

Experienced with IND/NDA submissions, and knowledgeable in regulatory guidelines (ICH), 21 CFR Part11 and Good Clinical Practice (GCP). * Highly experienced in clinical protocol development, experimental design, sample-size and power calculation, randomization, and study analysis planning (SAP). * Proficient in SAS/Base, SAS/Stat, SAS/Graph, SAS/Macro and SAS/ODS. * Skillful in data validation data manipulation, graph, tabl...

Tags for this Online Resume: Health Care Industry, clinical, protocol, sas, pharmaceutical, sap, ich, gcp, trial, phase, oncology

Registered Nurse - 15 Years of Experience - Near 60030

SUMMARY OF EXPERIENCE * Monitored Phases I, II, III, clinical trials in many therapeutic areas, including, but not limited to, Oncology, Cardiology, Dermatology, Infectious Diseases, Immunology, Women's Health, Gastrointestinal, Genitourinary, Neuroscience, in Adult and Pediatric (Otitis Media and Influenza) populations. * Managed multiple studies in various stages of conduct at as many as 15 study centers at any given time...

Tags for this Online Resume: Cardiology, Clinical Research, Dermatology, Gastrointestinal, Good Clinical Practices, ICH, Immunology, Infectious Diseases, Monitoring, Oncology

Clinical Pharmacovigilance/Drug Safety - 10 Years of Experience - Near 10591

To obtain a position as a Drug Safety Associate.

Ideal Companies: Regeneron, Pfizer, HHC NYC

Tags for this Online Resume: Distribution, Training, Data General Nova, Chemistry, High Performance Liquid Chromatography (HPLC), PEDIATRIC, Inventory, Inventory Control, Cancer, Chemotherapy, oncology, clinical, pharmaceutical, gcp, ich, protocol, phase, sas

Clinical Pharmacovigilance/Drug Safety - 10 Years of Experience - Near 19440

Summary Clinical Scientist/Clinical Data Analyst/Clinical Data Management/Project Coordinator/GLP auditor/Research Biologist with over 15 years experience in the pharmaceutical industry. Authored/QC review of protocols, protocol amendments, protocol clarification letters, informed consent forms, risk language, periodic safety reports (PSUR, DSUR, QSR), investigator brochures, medical monitoring plans, clinical SAE narrative...

Tags for this Online Resume: Protocol, Oncology, Audit, Monitoring, Critical Care - Neurology, ICH, Neurology, Quality Assurance, Test, Data Quality

Senior Clinical Research Associate - 20 Years of Experience - Near 92596

COVER LETTER: Dear Hiring Manager: My goal is to obtain a position where I can utilize my clinical research experience, sound knowledge of Good Clinical Practice (GCP), good judgment and analytical skills, attention to detail, creativity, international experience, interpersonal skills and reliability that are well suited to the needs of the Company and the Senior Clinical Research Associate position. My sound academic train...

Tags for this Online Resume: Analytical Skills, Clinical Research, Problem Solving, Problem Solving Skills, Public Health, Reliability, Research, Regional Clinical Research Associate, Data Queries, Audit, Clinical Trial, GCP, Protocol, Data Management, ICH, Phases I-IV