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Online Resumes with "Regulatory Affair "
Associate Director of Operations
Be able to work in an environment where I can help patients in a clinical environment as well as guide staff in providing the best care and clinical practices
Tags for this Online Resume: Clinical Operations, Provider Relations, Clinical Research, Documentation and Compliance, Regulatory Affairs, Quality Assurance, Quality Control
Clinical Regulatory Affairs Specialist - 3 Years of Experience
I am seeking to obtain a regulatory affairs position that will allow me to utilize the regulatory affairs skills - learned through education and experience.
Clinical Research - 14 Years of Experience - Near 37601
Tags for this Online Resume: Management , Time and expense report review and approvals, , Home office, Matrix reporting structure , Quality assessments, Budgeting, Successful FDA Audit-Clinical Regulatory Affairs/, Board Member --Treasurer ACRP Chapter in North East Tennessee Region
Director of Quality - 15 Years of Experience - Near 77086
10+ years medical device industry in variety of areas including Regulatory strategy for domestic and international marketing. FDA submissions of 510k and EU submissions of Technical Files for CE Mark. Implementation of Quality Systems per QSR, Health Canada, ISO 13485:2012, Medical Device Directive 93/42/EEC and Active Implantable Medical Device Directive 90/285.
Tags for this Online Resume: Quality Systems, Medical Device, Regulatory Affairs, 510K submission, CE Mark, Consultant, Director, Vice President
Clinical Regulatory Affairs - 15 Years of Experience - Near 60564
Clinical Regulatory Affairs - 14 Years of Experience - Near 19053
To obtain a rewarding position in the clinical research field which will broaden organizational, communication, leadership, and collaborative skills and provide an opportunity for further development
Tags for this Online Resume: philadelphia
Clinical Regulatory Affairs - 13 Years of Experience - Near 19711
My background includes 13 years’ experience in the Pharmaceutical Industry at AstraZeneca Pharmaceuticals in Global Regulatory Submissions and Life Cycle Management of Regulatory documents. This includes 6 years’ experience as a Project Manager for Regulatory Global submissions. As a Project manager within the Submission Management Group, I provided expertise on global submission compilation and published electronic submiss...
Tags for this Online Resume: Newark, DE, Life Cycle Management, Regulatory Global Submissions, Pharmaceutical Industry, RSS Application, eCTD Publisher, electronic submissions, Regulatory Publisher, Management, Cardiovascular, Document Management, Legal, Pharmaceutical, Project Management, Publishing, Quality Assurance
Operations Manager - 6 Years of Experience - Near 74112
Obtain a job within project and operations management field to utilize Bachelor’s degree, previous project and operations management work experience, expertise in good manufacturing practices, regulatory affairs, and superior communication skills.
Tags for this Online Resume: cGMP, GLP, Project Management, ERP, SAP, ISO9001, Regulatory Affairs, Technical Writer
Clinical Regulatory Affairs - 20 Years of Experience - Near 75063
Clinical Regulatory Affairs - 1 Years of Experience
Clinical Regulatory Affairs - 5 Years of Experience - Near 58102
Tags for this Online Resume: Medicare, Healthcare, SharePoint, PECOS, MS Office, MS Access, Me Excel
Clinical Regulatory Affairs
Professional, and is currently employed as a Regulatory Specialist. My attributes includes: multi-tasking with the ability to work independently and with a team; highly detail-oriented; good organizational and time management skills; ability to develop good customer and colleague relations; good management and interpersonal skills; solution-oriented; self-starter with a positive attitude and good communication skills. My sk...
Tags for this Online Resume: Clinical Research, Study Start-up, CCRC, CRA Experience, Leadership , GCP, CTMS, Research, Medical, Blood Bank, Telemetry, Nursing, Training, Business Development
