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Online Resumes with "Study monitor"



Experienced CRO management professional offering 20+ years of pharmaceutical toxicology experience

Looking for opportunities to excel in sponsor/CRO relationships. Last 10 years have been devoted to monitoring, managing, and building relationships with preclinical Contract Research Organizations (CROs) through demonstrated ability to plan, coordinate and interact professionally with all levels of staff both internally and externally. I possess excellent communication and interpersonal skills and have a firm understandi...

Ideal Companies: Biotech or pharmacuetical companies

Tags for this Online Resume: Preclinical Toxicology Outsourcing, Toxicology Account Manager, Preclinical Program Manager, Toxicology Study Monitor, Contract manager, CRO liason

Clinical research professional

Protocol Coordination • Study Management • Team Training • Process Improvement • Compliance Study monitoring • Protocol Implementation • Quality • Data Evaluation & Management • Reporting

Regional Clinical Monitoring, Kansas City, MO

To monitor clinical trials of all phases using extensive knowledge of drug development and regulatory processes. Experience: - study site selection and set up – preparation of pre-study regulatory documentation - preparation of site monitoring reports in accordance with specific timelines - follow-up and resolution of sites issues - identifies and assists sites with DCF resolution - maintains regular contact with ...

Tags for this Online Resume: Clinical Trial Manger, Clinical Research Associate (CRA), Medical Writer (MW), Project Manager, Clinical Research Scientist, Clinical Operation

Featured Profile

MD with clinical research experience, Virginia

Enter the pharmaceutical industry to advance my clinical research career. I see myself in a CRO or a pharma company, within the realm of clinical research study monitoring and eventually management. With substantial clinical experience, I also see myself as a strong pharmacovigilance candidate for a CRO or pharma company.

Clinical Research Manager, 19 years experience in Medical Device Industry

Looking for an opportunity to contribute and expand my skills in clinical research study management.

Tags for this Online Resume: study management, clinical research associate, clinical research, site management, Clinical research monitor, clinical study monitoring

Clinical Research Associate, Director, Clinical Research Manager

To make a promising career in the field of an organization where my hard work and dedication will take me to the cutting areas of my specialization contributing to the growth of the organization. Also, to join a company that offers me a stable and positive atmosphere and inspires me to enhance and therefore to innovate the work culture for the betterment of all parties concerned.

Tags for this Online Resume: Clinical Research Associate, Research Associate, Study Trial Specialist, Clinical Lead, Clinical Study Monitor, Clinical Trails

scientist toxicology preclinical pharmaceutical biotech drug development

Tags for this Online Resume: preclinical, toxicology, drug development, study director/monitor, pharmaceutical, scientist, study director, research scientist, study monitor

environmental scientist

Recognized expert in Contaminant Fate and Transport in environment specifically PCBs and chlorinated contaminants, as well as Hydrogeology with a specialty in Karst Aquifers having been trained under James F. Quinlan. Familiar with groundwater modeling with MODFLOW computer model. Proficient all areas of remediation including investigation, research, assessment, approval process, work plan development/implementation, collec...

Tags for this Online Resume: enviromental , scientist, geologist, hydrogeologist, remediation, investigation

Clinical Research Manager - 15 years Experience - Chicago

I am a nursing professional with 10-years medical and surgical critical care background who has 15+ years diverse experience managing pharmaceutical industry based clinical research projects and leading quality, training and new process implementation initiatives. I possess excellent organizational, data analytical and medical writing skills.

Tags for this Online Resume: Chicago, IL , Quality Assurance , Training , Clinical Research , project management , study monitoring

Clinical Research Scientist -4 Years of Experience - Near 46544

Tags for this Online Resume: Clinical research, Clinical Trial management, Clinical protocol, study monitoring, Clinical data base, Clinical Research Associate

Director, Human Research Protections - 17 Years Experience - Institutional Review Board Management - Human Subjects, Regulatory Education Development - Research Management, Department of Defense

I'm a Human Subjects Protection professional who has over 17 years of experience in managing research and regulatory programs. Extensive knowledge of regulations, writing and implementing policies and procedures, review of all study documents, training and development of staff, conduct of consent processes, subject education, and study monitoring.

Tags for this Online Resume: Institutional Review Board, Human Subjects Protection, Director, Manager, Department of Defence, Universtiy, Medical Center