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Online Resumes with "Investigational New Drug"

Featured Profile

Senior Director, Chicago

To obtain a leadership position for regulatory affairs expertise in the pharmaceutical/biotech industry

Tags for this Online Resume: regulatory affairs, pharmaceutical, biotechnology, clinical , manufacturing

Featured Profile

Registered Nurse - Drug Safety Associate,Coder, Product Surveillance/Product Safety

I am seeking for a stable and well established company that is growing. Also,what I am looking for in a new job is for employers that care about their employees and acknowleges them for their good hard work. I would also hope that good training is provided so that the individual such as myself can be productive for the company and contribute towards it's success rate. I would also hope that it was a warm welcoming environm...

Ideal Companies: Cephalon Pharmaceutical, Teva Pharmaceutical, Azur Pharmaceutical, GlaxoSmithKline, United BioSource

Tags for this Online Resume: Registered Nurse, Drug Safety Associate, Coder, Safety Surveillance, Adverse Event Coordinator


Having contributed to the success of major organizations by orchestrating expert alignment of scientific and business management resources with enterprise objectives, I am now seeking to join a company such as yours in the role of scientific writer. With more than 20 years of combined experience providing advanced leadership, delivering top level research and product development, and driving strategic analysis and planning...

Sr. Director/Director Clinical Quality Assurance and Compliance

Over 19 years of Regulatory / Clinical Quality Assurance & Compliance / Auditing experience. Maintain an excellent knowledge base of all applicable Guidelines, FDA Regulations as well as best practices. I have prior interaction with the FDA, and EMEA/MHRA authorities, leading to successful outcomes. I am considered to be a strategic leader and planner effective in a team environment and customer service focused, with exc...

Tags for this Online Resume: Clinical Quality Assurance, Compliance, Auditor, GCP, Quality Systems, Director

PhD - clinical research and laboratory science - 19 years experience

My career goal is to contribute to the development of new therapies using my experience and skills. After 5 years as Director of a laboratory which supports clinical trials I am ready for a change to a job which uses my expertise in clinical research data review, data summary, writing and communication. My job search is including but not limited to medical communications, consulting and project management.

Tags for this Online Resume: diagnostics, gene therapy, GLP, Investigational New Drug, clinical laboratory, Medical writing

Senior Life Scientist - 16 years Experience - Biotechnology - Colorado

A committed and highly accomplished biotechnology expert with 16 years of research and development experience, leading and supervising teams and managing a wide range of drug development projects for small biotechnology companies. Possesses knowledge and experience of pulmonary, cardiovascular, gastro-intestinal, and other disease indications and models. Vital skills and hands-on experience include science writing excellenc...

Tags for this Online Resume: Research and development, Writer, Communications, Science, Drug development, Supervisory, Biotechnology, Pharmaceuticals, Reports, Research, Team Leader, Project Management, Animal Models, IND, eCTD, Strategy, Recruiting, Drug Efficacy, Team, Management, Pulmonary, Gastrointestinal

Clinical Research - 20 Years of Experience - Near 60601

-Participate in development of new intramural clinical research studies, both for solid tumors and hematology/oncology, reviewed all new protocols, supervised designing case report forms for the new protocols for the solid tumors and hematology/oncology. -Work with the multiple investigators on developing and implementing new intramural oncology protocols and supervised accomplishments with all protocols' requirements. ...


Profile Experienced, highly motivated healthcare professional with notable accomplishments in clinical and basic research achieved in both academic and pharmaceutical industry arenas. Broad knowledge of all aspects of therapeutic product development. Extensive experience in strategizing and implementing global clinical research and development programs. Known for particular expertise and success in early clinical developmen...

Tags for this Online Resume: Clinical Research, Research, Cardiovascular, Endocrinology/Metabolism and Internal Medicine, Patient Care, Clinical Pharmacology, Protocol design/ Medical Monitoring, Budget Review, Budgeting, Board Certified/ Internal Medicine, Subspecialty-Endocrinology/Metabolism, Pharma/Clinical Research - Phase 1,2,3, Pennsylvania/ Pfizer (formerly Wyeth), Phase 1 and 2

Biology - 20 Years of Experience - Near 30341

Summary of Qualifications Experienced and highly qualified Scientist & Research Associate/Manager with over 20 years of experience in researching and teaching. Highly proficient in performing quality assurance control on laboratory best practices while leveraging R&D experience to consistently achieve project goals. Adept at supervising other scientists and research technicians in advancing stem and primary cell industry kn...

Tags for this Online Resume: Compliance, Chef, Filing, ISO, Management, Legacy, Microbiological Testing, Product Development, Reliability, Test

Biochemist - 18 Years of Experience - Near 21224

QUALIFICATIONS SUMMARY * cGMP quality management experience [ QA/QC and RA]. QA experience with quality management systems (QMS) and documentation, batch record reviews, annual product reviews, SOP drafting, review and approve, investigate deviation, change and document control. Established key performance indicators (KPIs), quality by design (QbD) process analytical technology (PAT) and Quality metrics. Experienced with de...

Tags for this Online Resume: Reviews, Chemistry, CMOS, Compliance, Documentation, Drafting, Product Development, Security, Systems Development, High Performance Liquid Chromatography (HPLC), pharmaceutical

Life Scientist - 20 Years of Experience - Near 20721

Summary * Project Officer and Work Assignment Manager human health toxicologist in the in the U.S. Environmental Protection Agency's (USEPA) Office of Water (OW) to support agency products registration and other regulatory activities * Developed human health benchmarks for registration/regulation of drinking water and environmental contaminants for the USEPA * Developed multivariate computational toxicology in silico QSAR m...

Tags for this Online Resume: Risk Assessment, Management, Toxicology, Integrate, biologist, toxicologists, Assessments, Cancer, Data Analysis, Database, ESA

Life Scientist - 15 Years of Experience - Near 20782

PROFESSIONAL SUMMARY Exceptional leader talented at building professional relationships, self-motivation and team goals. Technically-savvy with outstanding training and presentation skills. Motivated scientist with solid experience managing all levels of large scale projects, including budgeting and administration. Experienced Scientist professional with strong leadership and relationship-building skills. Meticulous Medical...

Tags for this Online Resume: Quality, Quality Assurance, Quality Control, Manufacturing, Cellular, Documentation, Electrophoresis, ELISA, Therapy, Training