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Online Resumes with "clinical QA"
Director of Nursing
• Liderchip, reorganized all aspect on this position, make Network Reports, Review Labs and Medications Adjust, Clinic Supervision, Review P&P and Update, make QIP report, Staff Schedule-Clinic, Monitor Staffing Patterns, Order Meds, Clinic QA, Review Patient Schedule, Review all Flow Sheets, Make in service Staff Required Topics, Make Hospitalization logs, Mortality logs, Infection logs, Staff Coverage, etc...
GCP-Auditor
I Kashinath, a Post Graduate in M.Pharm(Pahramacology) (Class of 2006) from Rajiv gandhi University with first class would like to submit my CV for the position of Quality Assurance / Clinical QA Monitor / Regulatory Affairs/Pharmacovigilence, in your esteemed organization.
Tags for this Online Resume: Clinical Reserach, Sr.RA-QA, BA/BE Studies
Quality Systems Manager/Director
Skilled leader with expertise in quality assessment, complaint management, both pre- and post-market product approval, associated regulatory reporting compliance, e.g., pharmacovigilance, field corrective action (FCA), and managing both internal and external quality assessment of operations. Designed, developed, reviewed and implemented quality, regulatory and operational systems. Developed and defined monitored account ...
Tags for this Online Resume: quality systems, regulatory reporting, quality assessment, field corrective action, complaint management, quality assurance
Clinical Research - 15 Years of Experience - Near 19438
Clinical research professional with over thirteen years of experience; including over six years as a Senior / Lead In House CRA and Field Monitor; over three years as a Quality Assurance Auditor and Quality Control Analyst; one year as an Assistant Manager, Clinical QA and nearly one year as a Drug Safety Associate. Currently seeking a Senior CRA or Junior Project Manager / Clinical Trial Manager position.
Tags for this Online Resume: Philadelphia , Senior Clinical Research Asssociate, Jr. Clinical Trial Manage
Clinical Research Associate
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...
Tags for this Online Resume: Clinical Research, Research, Accounting, Acquired Immune Deficiency Syndrome (AIDS), Advertising, Amazon Elastic MapReduce, Audit, Basic First Aid, BLS, Budgeting
Regulatory Affairs Specialist - 16 Years of Experience - Near 19464
An accomplished records and information management specialist with proven skill set including 16 years’ experience within records retention and information management. Focus on health authority audit preparedness, compliance, security, and lifecycle management requirements of key company proprietary media encompassing all GXP documentation. Actively liaise with internal areas and external groups including CMOs and CROs to ...
Tags for this Online Resume: Filing, Management, Quality, Quality Assurance, Quality Control, Retention, Document Management, Documentation, Information Technology, Records and Information Management, Regulatory, Operations, Record Coordinator, Compliance, Regulatory Operations
Psychology - 17 Years of Experience - Near 92057
Clinical Assisted Director of Operations in the daily operation of all trials at the Site. Responsible for staffing and training study personnel and planning study start-up activities. Responsible for team performance and annual goal reviews. Responsible for client relationships through obtaining feedback from trial monitors and sponsors. Trials was an outpatient Phase 2-4 clinical research facility with a 4-bed sleep labor...
Tags for this Online Resume: Management, Process Improvements, Risk Management, Clinical Operations, Clinical Research, Research, Pharmaceutical, clinical, phase iv, phase iii, pharmaceutical, quality, clinical QA, GCP, document control, clinical trials, IRB, consent document, essential documents, nonessential documents, SOPs, Work Instructions
Clinical Research
Ideal Companies: Clinical Research Organization, Biotech/Pharmaceutical Company
Tags for this Online Resume: Filing, Management, Compliance, Cancer, Quality, Quality Assurance, Quality Control, Test, Clinical Research, Research
Clinical Research
Tags for this Online Resume: Audit, Management, Documentation, Fraud, Pricing, Regulatory Affairs, Research, Security, Test, Assessments
