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Online Resumes with "Drug development "



Senior Medical Scientist

I am a Medical Scientist with extensive clinical development experience and a proven track record of successful contributions to the approval of multiple new drug applications (NDA/BLA). I have a strong foundation of global drug development and extensive experience conducting clinical trials in accordance with local, country-level and global standards. My experiences range evenly from early to late stage clinical developmen...

Tags for this Online Resume: Cancer, Statistical Analysis, Cardiovascular, Chemistry, Diagnostics, Filing, Immunology, Integrate, Management, oncology, trial, pharmaceutical, clinical

Clinical Research - 9 Years of Experience - Near 45999

- 3 clinical research studies while developing an understanding of the drug development process Good Clinical Practices and relevant regulations. Perform management of study site activities to ensure the integrity of clinical data in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs). New experience oncology trials (lung cancer melanoma antigen-specific immune-therapeutics) RDE (elect...

Tags for this Online Resume: Clinical Research, Research, Oncology, Overdose, Cord Injury, SAP MM module, Application Support, Good Clinical Practices, Management, Support

Statistical Programmer - 5 years Experience - US

Summary * Certified Base Programmer for SAS 9 with 5+ years of biostatistical programming experience in CRO, hospitals, pharmaceutical, and healthcare industries. * Involved in drug development process with experience in analyzing, reporting, and reviewing pre-clinical/clinical trial data. * Good understanding of FDA submission (IND, NDA) process, clinical protocols, CRFs, CDISC (SDTM, ADaM), 21 CFR Part 11, GCP, and IRB gu...

Tags for this Online Resume: SAS, Proc, Programming, Statistical Analysis, SAP, Research, Statistics, Structured Query Language, Management, Test

Programmer Analyst

SUMMARY * 6 years of experience as a Statistical Programmer in Clinical trials of Pharma Industry. * Expertise in SAS programming features like BASE SAS, SAS/MACROS, SAS/STAT, SAS/GRAPH, SAS/SQL, and ODS. * Skilled in generating reports featuring various SAS procedures, like Proc Report, Proc Summary, Proc Freq, Proc Mean, Proc Transpose, Proc sort, Proc Univariate, Proc Datasets, Proc Compare, Prco SGPLOT, and Proc SQL. * ...

Tags for this Online Resume: Base SAS, Macro (Predefined Code), Proc, SAS, SAS/STAT, Statistical Analysis, Structured Query Language, Data Analysis, HyperText Markup Language, Microsoft Excel

Chemist - 8 Years of Experience - Near 08855

SUMMARY: * Over 16yrs pharmaceutical experience in Quality Control, Stability and R&D, Drug development & approval, sterile injectable pharmaceutical manufacturing, solid dosage manufacturing, aseptic techniques, and clinical packaging/ labeling for top pharmaceutical companies. * Solid background in Instrumental Analysis and GMP compliance. Expertise in hands-on use of instrumentation such ICP, GC/MS, HPLC, LC/MS, UV, and ...

Tags for this Online Resume: High Performance Liquid Chromatography (HPLC), Research, SEC, Securities and Exchange Commission (SEC), Support, Instrumentation, Audit, Good Laboratory Practices, Good Manufacturing Practices, oncology, phase, protocol, pharmaceutical, clinical

Assay and drug developer, biophysical chemist, live cell imaging specialist

I am looking for the opportunity to bring my knowledge, experience and passion for scientific work to research and development projects within Biotech/Pharmaceutical company

Director

Strategic, analytical and forward-thinking leader with significant experience in managing the design, construction, contract administration, oversight of client/ building officials and operations of very large, technically advanced and complex facilities. Excels at team building, readily earns the respect of the client and enjoys a reputation for bringing projects in on schedule, within budget and in compliance with contrac...

Tags for this Online Resume: Director, Regulated Environment, Senior Program Manager, Contract Administrator, Senior Facility Manager, PMP, Manufacturing, Life Sciences, Preventive Maintenance, Integrate, Quality Assurance, Reliability, Research and Development

Admissions Director - 0 Years of Experience

SUMMARY * Pharmacovigilance Associate with over 2+ years of experience in Drug Safety and Clinical practice fields with clear understanding of EDC (Electronic Data Capture) * Experience in performing successful data management, triage, case entry, MedDRA, WHOdrug dictionaries, narrative writing, peer review, case follow-up, case review and report preparation * Performing Data entry and Quality check adverse event reports fr...

Tags for this Online Resume: Quality, General Practice, HYGIENE, Medical, Surgical, Acceptance Testing, Assessments, Business Intelligence, Coding, Database, healthcare

Life Scientist - 16 Years of Experience - Near 92069

Innovative and results-driven scientist with over 16 years’ experience & proven track-record in the pharmaceutical / biotech industry seeking senior managerial position to establish and direct preclinical drug discovery research.

Tags for this Online Resume: Neuroscientist, Pharmacologist, Histologist, Imaging specialist, San Diego, Drug Development, Atlas, Neurological, Research, Pharmacology

Clinical Research - 20 Years of Experience - Near 07042

Summary: * Expertise towards drug development and FDA, GCP/ ICH regulatory guidelines in the pharmaceutical industry Strong experience in a drug development performing different phases of clinical trials and Supported CTH in managing interactions with relevant line functions including Data Management, Drug Supply Management and Novartis Country Organizations and also performed Monitored pre-study, initiation, interim, close...

Tags for this Online Resume: Clinical Research, Research, Oncology, Query, Cardiovascular, Filing, Management, Database, Database Maintenance, DSS

Chemist - 10 Years of Experience - Near 90808

Qualifications Profile A responsive, organized, and detail-oriented team player with excellent oral and written communication skills with eight years of strong chemistry laboratory experience in a pharmaceutical research organization for drug development of small molecules with three years of experience in chemistry laboratory quality assurance in GLP/GMP, and one year as an analytical chemist in a manufacturing setting.

Tags for this Online Resume: Audit, Documentation, High Performance Liquid Chromatography (HPLC), Management, Quality Assurance, Test, Cardiopulmonary resuscitation (CPR), Chemistry, Communication Skills, ELISA

Business Analyst

PROFESSIONAL SUMMARY: * Experienced in utilizing QlikView's dynamic update functionality for real-time reporting. * Expertise in working with diverse business users to understand the requirements and develop a robust data model that will support the current requirements and future business growth utilizing Agile Methodology. * Expertise in Powerful map visualizations and location-based analytics for both Qlik Sense and Qlik...

Tags for this Online Resume: Business Requirements, Microsoft Excel, Microsoft SQL Server, Structured Query Language, Distribution, Microsoft Windows, Oracle, Acceptance Testing, Agile Methodologies, Agile methodology