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Online Resumes with "Clinical Site Management"
Clinical Project Manager with 18 years of diverse site monitoring and study project management. I specialise in data trend analysis and are duel certified as a CRA and Site Auditor. Responsible for 5 direct reports.
I am willing to take challenges and always go beyond boundaries to solve the the problems.
Tags for this Online Resume: Clinical Project Management , Clinical Financial management , Clinical Vendor management , Clinical Trial supply management , Clinical site management, Clinical Risk Management
SUMMARY: To apply my knowledge of FDA Good Clinical Practice guidelines/ICH guidelines, extensive site/field Clinical Director, Site Lead Study Management, in addition to my experience with various therapeutic areas of medicine, to a position as a Clinical Research Associate. AREAS OF EXPERTISE * Management * Interview candidates and either make a selection decision or recommend individuals for hire. * Able to manage multip...
SUMMARY Clinical Research Professional with more than 20 years experience in Phase II-IV clinical site management, regulatory compliance and monitor training for major pharmaceutical companies. Demonstrated expertise in electronic systems including CTMS, EDC, IVRS, CRF design, query management and corporate communications. Proven success in all aspects of clinical trials from study start up through close out in phase IIb-IV...
Pamela's objective is to acquire a home-based/telecommute position within the clinical research field. Areas of primary interests are line manager, in-house CRA or regulatory affairs; however, open to other options. Her skill sets and work ethic are highly applicable the the clinical research arena
Tags for this Online Resume: Query, Audit, Data Queries, Email, Employee Relations, Human Resources, Medical, clinical, phase iii, phase iv, phase ii, phase i, research, clinical trials, pharmaceutical, cro, regulatory, resourcing, study lead, Sr. CRA, In-house CRA, Line Manager, Clinical Site Manager, devices, clinical coordinator, psychiatry, occupational therapy, job placement coordinator, job skill evaluator, customer service, bid defense, banking, sales, trainer, supervisor
A top-performing Senior Clinical Research Associate with extensive experience in clinical research, GCP, ICH, Regulatory, and clinical site management/monitoring. Solid background in critical care nursing for in-depth understanding of medical terminology for records review. Highly skilled in spearheading internal teams through clinical research and document management to ensure accuracy and adherence with study specific str...
Tags for this Online Resume: Clinical Research, Management, Protocol, Research, Documentation, Medical, Allergy, Monitoring, Reporting Tools, Cardiology, clinical, trial, gcp, protocol, pharmaceutical, regulatory, medical device, CNS, EDC, contract, remote, CRO
I am a Regisered Nurse with interests and experience in Clinical Regional Monitoring and Clinical Management/Project Manager - 15 Years of Experience - Near 06512
I have a strong clinical background as a Registered Nurse prior to my joining the pharmaceutical industry. This has been beneficial in the course of my career. I have expertise in many areas and observational abilities in tracking subject safety and tolerability. I am aware of site challenges, having conducted clinical trials in large hospital settings as an RN and can be supportive and provide suggestions to sites when ch...
Ideal Companies: DOCs ICON Pfizer
Tags for this Online Resume: Clinical Research, Oncology, Immunology, Neuroscience, CRA, Registered Nurse, Clinical Manager, Data Management, Clinical Oversight, Project Management, CRO, CRO Oversight, GCP, ICH, Pharmaceutical Industry, Clinical Site Management, Compliance, Safety Management, Site Selection, Regulatory Compliance, Continuous Quality Improvement, Medical Writing, FDA Reporting, Trial Master File/eTMF, Cross-Functional Facilitation, Strategic Planning, Risk Analysis, Safety Oversight and Reporting, Data Targeted Review