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Online Resumes with "Essential Documentation"
Community education and support
Maturity and experienced in interpersonal skills, negotiations and problem solving
Ideal Companies: non profit agencies, development of community services, public relations
Tags for this Online Resume: social services, social services/community
Construction electrical engineer - 5 years experience / Telecommunication (FO) engineer - 6 years experience
My interest in Buildings achieved and developed during my work in Bechtel International Company. Duties included the assessment of power, lighting, IT, Fire Alarm, Intercom and Access Control Systems, viewing shop drawings of all the systems above and responsible for providing all the essential documents. Also intrested in Fiber Optics, My responsibilities were to lead a crew of engineers and supervise subcontractor wo...
Tags for this Online Resume: Fiber Optics Engineering, electrical engineering
Essential Document Specialist/Training Specialist - 22 years in Pharmaceutical
My goal would be to find a placement where I would be able to share my personality and motivational speaking ability to help make a difference. I love working with people, and enjoy the challenge of making their every day responsibilities more exciting!
Customer Service Manager
I am a dedicated customer service representative, with the talent to build prolific relationships, resolve intricate issues, and win customer loyalty. I listen attentively, solve problems creatively, and use tact and diplomacy to find common ground and achieve win-win outcomes. I am looking toward the future in hopes to work for a company that recognizes the importance of providing excellent customer service to retain clien...
Ideal Companies: Bluegreen Corporation
Tags for this Online Resume: Manager, Customer Service
venky
• 9 Years of basic research experience (Clinical Molecular Biology and Bio-Chemistry) • Excellent organization skills • Detail oriented • Solid knowledge of microbes and anti-infective therapy • Leader of quality assurance team ensuring adherence with state and federal regulations • Ability to work as part of a team or independently • Solid knowledge of adherence to federal and state regulations (JACHO) • Indust...
Ideal Companies: Pharmaceuticals, Biotech, contract research organisation
Professional Eng'r, tech writer, editor
To produce essential documentation
Trial Master File/Document Quality Coordinator
I am a Document Quality Coordinator/Clinical Trial Assistant with 3 years experience with pharmaceuticals and 3 years with CROs. My expertise in with organizing, maintaining, and quaity checking Investigator files and General files, hard copies and electronic documentation. I keep track of updates on essential documents from sites - IRB approvals, CVs, Medical licenses, and Financial disclosures,protocol, IB, study manual ...
Tags for this Online Resume: trial master file, clinical assistant, data enty, filing
Senior Technical Writer/Requiements Analyst - Over 15 years experince in Northern, VA
Find a position where it will be possible to mentor, train others, and utilize my extensive skills to benefit an organization in Northern, VA. Would also like the ability to work remotely on occasion.
Ideal Companies: Information Technology (IT) concerns, and Government contractors
Tags for this Online Resume: ITIL, MS Office, Visio, CMMI, Analysis/Design, RoboHELP, SharePoint, Documentation
Clinical Pharmacovigilance/Drug Safety - 2 Years of Experience - Near 27713
Tags for this Online Resume: FDAguidelines, Medical writer, ICH GCP, Essential documents, Regulatory guidelines, E3 guidelines, Investigator brochure, ICF
Clinical Regulatory Specialist
Looking for an opportunity that will allow me to share my skills and experience for the betterment of our global community. I have worked in this arena for quite some time and I know how to avoid the pitfalls surrounding clinical trials to ensure deliverables are met and compliance and efficacy is adhered to on every level of the study timeline.
Tags for this Online Resume: Clinical Trials , IRB Submisssion, Compliance specialist, Willing to Travel, Regulatory Document Reviewer, Essential Document reviewer, Informed Consent Reviewer, Management, Clinical Research, Ethics Committee Submission experience
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
Clinical Research - 10 Years of Experience - Near M1T3N
SUMMARY: * NIH trained Study/Site Coordinator with 10 years of experience in clinical research coordination and administration. * Demonstrated ability in coordinating & implementing Network / Pharmaceutical / Investigator-driven multisite Phase I - IV clinical studies. * Adept in liaising with internal and external stakeholders.
Tags for this Online Resume: Protocol, Clinical Research Associate, Infectious Diseases, ICHGCP, Logistics of study material, Monitoring, Data Entry, Team Lead, Essential Documentation, Informed Consent, SOPs, Coordinator, Regulatory, QA/QC, Source Docmentation, CRF's, TMF, EDC, Toronto, Contracts, SAE
