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Online Resumes with "study protocols"



GLP Quality Assurance Auditor

Promote compliance with all GLP regulations, including IACUC and internal policies, procedures, state and federal regulations. Audited complex systems, facilities, study protocols, validation plans, raw data, in-life critical phases and final reports in the ABSL-2, 3 and 4.

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Versatile Bio-Tech Researcher w/ real leadership experience!

Supervise a team of technicians with various certification levels. Responsible for overall management and conduct of all studies assigned to Large Animal Group. Assumes fiscal responsibilities for assigned studies, is aware of study timing and materials need projections. Acts independently carrying out all in-life study functions as assigned. Ensures that duties are performed according to protocol requirements and adher...

Ideal Companies: Novartis, Pfizer, Abbott, Johnson & Johnson

Tags for this Online Resume: Detailed-Oriented, Leader, Problem Solver, Passionate, Clear Communicator

Registered Dietitian, Certified Diabetes Educator

High-powered, compassionate, and versatile healthcare professional equipped with more than 20 years of experience in Clinical Research, Diabetes Education, and Program Coordination. Show competency to manage delivery of clinical study protocols, clinical study reports, study agreements, applications, and other study documentation. Demonstrate strong analysis, research, documentation, and advocacy expertise, coupled with eff...

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Regulatory Compliance Specialist

Ideal Companies: MedImmune, NIH, Social & Scientific Systems

Tags for this Online Resume: triage, clnical trials, auditing, informed consents, study protocols, communications

Clinical/Program Coordinator

I am looking for a position which allows me some direct contact with patient/subject populations, but also gives me the opportunity to mentor new young professionals entering the research management.

Ideal Companies: Dept of Public Health, research

Clinical Trials Associate

Michelle Straka, BSHS, CPT 1163 Portsmouth Circle Medina, Ohio 44256 Cellular: (216) 337-2007 Home: (330) 722-2165 Email: dodgestealthrt1994@yahoo.com Linkedin account: http://www.linkedin.com/pub/michelle-straka/1b/964/aa2 Objective Obtain the position of Clinical Research Associate to further advance monitoring career. About four years additional experience in research as a study coordinator, regulatory coordina...

senior research scientist and writer

A position as a consultant or freelancer to generate and/or edit scientific and technical reports, manuscripts, presentations, and any other documents associated with academic or corporate activities. Direct or consulting activities to develop and execute scientific or technical study protocols, data analysis, and presentation of results through different routes of dissemination. Participate in professional meetings and com...

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Multi-service Staff Nurse/Research Study Coordinator/Nurse Manager

To find a challenging Nursing position offering opportunities for Self-initiation, Experimental Growth, and Career Advancement.

Ideal Companies: Center for Life Management, Catholic Medical Center, Elliot Hospital, Parkland Hospital, Dartmouth Hitchcock and Federal Employment Companies

Tags for this Online Resume: Registered Nurse, Nurse Management, Medical Specialty Services, Research Study Coordinator, Pulmonology, Community-based nursing services, Electronic health record documentation, Self-directed and motivated, Demonstrates and promotes professional and personal integrity, Respects each patient, Ability to communicate effectively and compassionately with patients and their family members, Strong interpersonal skills, Leadership in the application of the nursing process, Collaborates with other professionals across disciplines both within and outside the Medical Center, Acts as a consultant within the clinical practice area, Creative approaches to enhance quality of care and productivity of providers, Public relations efforts continue through active participation with community groups providing ongoing education

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Biologist- 12 years experience - West Point, PA

Highly organized, self-motivated Research Biologist with 12 years’ experience in pharmaceutical research conducting preclinical studies in 5 animal models. Recognized for excellent communication and technical skills, ability to adapt to unexpected circumstances and effectively prioritize tasks; works well in a group and independently.

Ideal Companies: Merck, Johnson & Johnson, GlaxoSmithKline, Charles River, Icon, Other smaller CROs

Tags for this Online Resume: Preclinical Toxicology Studies, Data Management, Animal Research, Documentum, First Doc, GLP guidlines and FDA regulations

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Statistician/Biostatistician and Data Modeler for Decision Science.

Seeking career opportunities in a field integrating Statistics/Biostatistics, Data Mining, Data Modeler, and Decision Science.

Ideal Companies: Pharmaceutical companies; and Health Insurance companies.

Tags for this Online Resume: Data Mining, Medical Records , SAS, SQL, database, clinical Trials, Healthcare, analysis, Management, Biostatistics, Data Modeler

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Clinical Research - 6 Years of Experience - Near 92649

Experienced Clinical Research Professional interested in positions within the pharmaceutical or medical device industry.

Ideal Companies: inventiv, johnson & johnson, covance, covidien, peregrine

Tags for this Online Resume: Irvine, CCRP, regulatory affairs, clinical project manager, EDC, budgets , timelines, contracts and budgets