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Online Resumes with "Good Clinical Practices"
A highly motivated methodical and analytical professional, precise and attentive to detail; "Going by the book", Loyal and dedicated; organisational and problem solving skills which has brought added value in projects undertaken.
I am seeking opportunities to contribute as a scientist within preclinical drug development or drug discovery research for the bio-pharmaceutical industry to support the primary or secondary screening and characterization of the molecular mechanism of action of lead drug candidates enabling target validation. I specialize in the development of cell-based assays using genomic, proteomic and biochemical approaches implementin...
Tags for this Online Resume: Lentiviral Retroviral shRNA RNA knockdown screens, Flow Cytometry, RTPCR, Immunopreciptations, Reporter assays, Cell based Assays, ELISA, Migration, Stable and Transient Transfections, Genomic and Proteomic Studies, Cloning, Transient siRNA knockdowns, Phenotyping Mammalian cell lines, Gene Overexpression, Subcloning to expression Vectors, Construct Stable Inducible Cell lines, Protein Kinase Assay, Pulse Chase Experiments, Transfection, Transduction, Transformation, Polyoma virus DNA tumor virus replication, Research Scientist, Cell Biology Protein Biochemistry Genetics Molecular Bioliogy Oncology Virology, FACS
Dedicated to helping both people and organizations reach their highest potential, I am seeking to apply my extensive experience and knowledge of program development, human services, and organizational leadership and management to secure a challenging position contributing actively to employee and company success.
Tags for this Online Resume: Efficiency Improvements, Data and Trend Analysis, Organizational Assessment and Development, Program Design and Management, Policies and Procedures, Service Level Optimization, Problem Solving, Industry and Regulatory Research, Team Building, Independent and Group Development, MS Office (Word, Excel, Access, PowerPoint)
Dedicated, outcome-focused, and skilled professional with broad-based perception and exceptional skills in clinical research, encompassing trial monitoring, site management, audits, and detailed record keeping. Interested in pursuing a challenging career as a Clinical Research Associate to utilize commendable multitasking proficiencies and technical documentation expertise. Commended for demonstrating a collaborative leader...
A quality assurance professional with over 25 years experience in the areas of auditing , Good Clinical Practices and Good Manufacuring Practices and project managment. As a quality professional strong knowledge of quality standards for controlled document managment, corrective action and process deviations, and internal and external auditing.
New windows of opportunities to advance clinical research
Tags for this Online Resume: Clinical Research, Electronical Medical Record, Data Management , Clinical research Compliance, Good Clinical practices, Good Documentation Practices, Faculty Healthcare Administration
I am a recent graduate with a degree in biology who is interested in clinical research. I currently volunteer at Toronto General Hospital in Palliative Care where I perform clerical duties. I have a strong knowledge in Good Clinical Practice and I am interested in clinical trials of cancer research.
Emergency Medical Technician - Graduate education with Research Experience - Over 2 years experience in clinical setting
I am a motivated individual seeking to begin a career in the healthcare industry utilizing experience from patient care, laboratory research, and project management skills.
I am a Clinical Research Manager that has extensive experience with Good Clinical Practice and the related regulations to maintain a quality research program.
Cover Letter Ignace Vallejo, MS. GCP and GMP QA Manager Certified Quality Auditor GMP; by CFPA. Certified Six Sigma “Black belt”. 525 Neptune Ave, Brooklyn, NY 11224. Apt 22 F Home # 718 946 0556. Mobile # 917 359 3028. firstname.lastname@example.org Good Clinical Practice (GCP). Audits were followed according to our SOPs and ICH GCP regulations and Guidelines. The vendor audits were preformed, as follows: • On Octo...
Tags for this Online Resume: biomedical engineer, healthcare, electronic medical records, biomechanics, regulatory compliance , clinical research, quality , project management of medicaldevices, medical devices, applications engineer, design engineer, product engineer, regulatory affairs, good clinical practice, quality compliance, medical imaging
Matthew Thomas Marcum 3220 N. Ruth Avenue • Cushing, OK 74023 email@example.com 918-225-2977 Dear Sir/Madam, I am a recent graduate from Johns Hopkins University (cum laude) with an M.S. in Biotechnology who is currently seeking a challenging and exciting career within the Clinical Research sector. Moreover, I possess a robust education in drug discovery and development, clinical trial design, clinical ethics, Good Clinic...