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Online Resumes with "Covance"
Accomplishments: Consistently led all teams to exceed net sales and market share growth targets for nation in all targeted therapeutic disease states. Led department from below 10 ranking by customers in Scott-Levin rankings to #1 ranking. Led a small but focused group in obtaining the first ever preferred access within United Healthcare
Tags for this Online Resume: Account Management, CVS, Defense, Evaluate, Management, Medicare, Microsoft Access, Pharmaceutical Industry, Prime, Staffing & Recruitment, Access, Reimbursement, Pull Through
SUMMARY OF QUALIFICATIONS CRO professional specializing in central laboratory operations and clinical trials data management. Resolves issues by building consensus. Strong customer relationship skills developed as a service provider to the biopharmaceutical development community. Experience directing international teams to develop business intelligence enabling integrated business/IT strategic planning.
Tags for this Online Resume: Protocol, Management, Project Management, Applications, Information Technology, Business Development, Electronic Data Interchange, Insurance, clinical trials, cro, Data Management, Informatics, Innovation, Vendor Management, Business Process Management
To find expand on my role as a Lead Clinical Research Associate. I am seeking either full time or contract work.
Tags for this Online Resume: Oncology, Cardiology, Drug, Device, Advertising, Documentation, Financials, Audit, Clinical Operations, Complaints, Medical, Medical Devices, Advertising, Documentation, Financials, Audit, Clinical Operations, Complaints, Medical, Medical Devices
1 years 10 years 12 years 5 years 2 years 6 years 5 years 7 years 7 years 3 years 1 years 1 years 1 year 4 months * * * * * * *
SUMMARY OF QUALIFICATIONS: Expertise working in a regulated environment following Good Laboratory Practices (GLPs), Good Clinical Practices (GCPs) and Standard Operating Procedures (SOPs) in both analytical and animal toxicology laboratories. Maintains and oversees sample management operations including the Rees environmental monitoring system, Watson sample acquisition information and tracking of GLP Bioanalytical & Immuno...
PROFESSIONAL SUMMARY * Experienced Compliance Reviewer, Quality Control and QA Specialist. * Manufacturing professional with 17 years in GMP controlled manufacturing suites and lab environment seeks a position offering professional growth and stability. * Thrive in challenging environments and am always seeking new ways to improve workplace efficiency. * Skilled in validation of laboratory instruments including those with c...
SUMMARY An experienced Senior Clinical Research Associate with considerable Local, Regional, and US experience within the CRO environment. Key experiences are within Endocrinology, Neurology, Cardiovascular, Infectious Disease, Bone, and Oncology. * EXPERIENCE * PRA Health Sciences August 2016 - October 2017 * Job Title: Sr. Clinical Research Associate * A member of a CRO team dedicated to a major sponsor program to evaluat...
Desire a position performing the negotiations of the contracts and budgets, confidentiality non disclosure agreements and other related documents, development of templates using sponsor/client and employer processes and guidelines. Have worked remotely or as self employed since 2007, so have proven to be highly organized, self-starter, able to work with little supervision. Would prefer a remote position.
Ideal Companies: Premier Research, Medpace, Fisher Clinical Services, Pharmatek Labs, PRA Health Sciences, Iqvia, Icon, inVentive Health, Premier, Quintiles, Charles River Laboratories, Neurocrine, PPD, Synteract