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Online Resumes with "Crf"



General - 1 Years of Experience - Near 18944

Summary of qualifications Highly effective in promoting a positive, productive environment. Developed innovative programs for major eClinical firms, incorporating trends on the leading edge of data management and eCRF design in the clinical research industry. Well organized and focused in coordinating projects for self and others. Skilled and thorough in analyzing problem situations and finding creative solutions. Advocate ...

Tags for this Online Resume: Standards, Process Improvement, Competitive Analysis, Product Management, Data Management, Management, Program Management, Project Management, Thought Leader, Requirements Definition

Clinical Research - 1 Years of Experience - Near 55102

Tags for this Online Resume: Device and pharmaceutical research, Clinical Research, 21CRF, Preclinical Research, ACRP, ISO 9000, FDA, GCP, Patient Care

Clinical Project Manager-6 years-France

I supervised the development of several clinical projects in different therapeutics areas and in different countries (France, England, Italy, USA and Canada). I coordinated the clinical activities in respect with the budget, timeframe and regulations (SOPs, FDA-GCP and ICH guidelines). I trained CRAs, site investigators and CROs to ensure study protocol comprehension and compliance (initiation visits, co-monitoring). I plan...

Tags for this Online Resume: clinical project, oncology, dermatology, cardiology

Clinical Research - 7 Years of Experience - Near 10803

Qualification Highly motivated and accomplished Clinical Research Coordinator with extensive skills and experience. Nine years of experience as an Oncology research coordinator. Proven ability to manage multiple studies simultaneously. Managed phase 1b - IV protocols according to GCP and FDA guidelines. Experience as a supervisor and mentor to study coordinators across various oncology disease sites. Trained staff on study ...

Tags for this Online Resume: Appraisals, Audit, Clinical Research, Data Quality, Documentation, Management, Protocol, Quality, Quality Assurance, Recruiting

Medical or Health Services Manager - 10 Years of Experience - Near 07436

Professional Summary * Detailed clinician with over 10 years Medical Technologist experience performing complex detailed testing in a clinical research laboratory setting. Investigator initiated research projects with compliance background. * Skilled Pharmacy Technologist with over 10 years' experience in pharmacy leadership, technology, and drug development * Diligent, accurate and reliable Laboratory Technologist with a r...

Tags for this Online Resume: ELISA, Protocol, Cardiology, Compliance, Critical Care - Neurology, Critical Care - Vascular, Data Analysis, Good Clinical Practices, Insulin, Management

Programmer Analyst - 8 Years of Experience - Near 22042

PROFESSIONAL SUMMARY * Over 8 years of experience in Information Technology field with strong emphasis in SAS Application Analyst/ Programmer with 3+ years of hands on experience and professional experience in Clinical Trial projects and also worked as Application Analyst in the CROs, Healthcare and Pharmaceutical industries. * Experience in analyzing and coordinating clinical data, generating detail summary reports and dat...

Tags for this Online Resume: Management, Oracle, Oracle 9i, Information Technology, Process Improvements, Coding, Health Care Industry, HyperText Markup Language, Manufacturing, sql, SAS analyst

Clinical Research - 20 Years of Experience - Near 27517

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...

Tags for this Online Resume: Protocol, Clinical Research, Research, Audit, Training, Clinical Research Associate

Developer - 12 Years of Experience - Near 22180

Summary: * Over 12 years of experience in Data Analysis using SAS. * Experience in complex BI Reports, Dashboards using latest BI tools like Tableau, SAS, Developing Performance Dashboards, Score cards, Metrics, What if analysis, Prompts, Drills, Search (using Add-ons), and Reports/Dashboards for all the functional areas using Tableau. * Eight years of experience in the Financial Services Industry. * SAS certified in Predic...

Tags for this Online Resume: Macro (Predefined Code), Structured Query Language, Microsoft Access, Proc, SAS, SAS/ACCESS, SAS/STAT, Base SAS, Management, Microsoft Excel

Certified Clinical Research Coordinator - 13 Years of Experience - Near 34202

Seasoned Certified Clinical Research Coordinator with 13 years' experience as a CRC, including experience in marketing, advertising, and regulatory document completion and submission. Completed my duties with great attention to detail, compassion, professionalism, confidentiality, and care. Seeking a position in healthcare/clinical research/pharmaceutical industry that will allow me to continue to exercise these skills and ...

Tags for this Online Resume: Clinical Research, Research, Good Clinical Practices, Protocol, Advertising, Documentation, Marketing Management, NPI, Training, Accounts Payable, clinical, trial, phase, gcp, protocol, pharmaceutical, GCP, IRB, CRF, ich, AE, SAE, SUSAR, Inclusion and Exclusion Criteria, ECG, Biological, PK, PG, Substudy, ICF, EDC, Rater, concomitant medications, IP, IP accountability, regulatory documents, master file

Medical Office Manager - 5 Years of Experience - Near 27502

QUALIFICATIONS: * Promoted to the Senior CRC position as the youngest individual within the organization due to ambition, diligence, a strong team player with the ability to look at the big picture and plan accordingly. * Developed strong CRO/sponsor/vendor relationships, ensuring continuity and open communications through all phases of the trials. * Continuously reached study goals by collaboration with a diverse populatio...

Tags for this Online Resume: Cardiology, Clinical Research, CMA, Communications, Management, Medical, Project Management, Research, Triage, Research Protocols, IRB, Informed Consent, Mentoring

Quality Coordinator - 6 Years of Experience - Near 60504

PROFESSIONAL SUMMARY: * Total of 9.5 years of experience in Health Care industry. 6 years' experience in Clinical Data Management. * Worked as a Clinical Data Coordinator in Quintiles Technologies from Feb 2011 to Aug 2014. * Worked as a Clinical Data analyst in PAREXEL International from Aug 2008 to Feb 2011. * Also, I have 3.5 years of experiences in Medical Microbiology field in health care sector I started my career as ...

Tags for this Online Resume: Data Management, Health Care Industry, Management, Microbiology, physical therapist

Postsecondary Teacher - 11 Years of Experience - Near 29376

CURRICULUM VITAE: Sharon Woodruff Team excellence instructor, facilitator, and trainer. Proven managerial, interpersonal, and training skills. Work History Title: Senior Clinical Research Associate Company/Location United BioSource Corporation Kansas City, MO/Regional United States Dates July 2014 - January 2015 Accountabilities Implement and monitor clinical trials for medications and devices to ensure sponsor and invest...

Tags for this Online Resume: South Carolina, Training, New Hire , Business, Education, Postsecondary, Excellence