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Clinical Research Professional

$80/hr Starting at $25

LAH Clinical is a Consulting Research Organization that provides clinical research, administrative, medical and scientific services to pharmaceutical and biotechnology companies, private organizations, Government agencies, Non-Governmental Organizations (NGOs), Medical Institutions and other similar industries. LAH Clinical provides the following clinical, administrative, and medical services to its clients: Clinical Research Services • Clinical Research Management of Phase I through 4 Clinical Trials • Clinical Project Management • Trial Master File (TMF) Development, Set-up, Maintenance and Management • Clinical Document Management • Drug Master File (DMF) • Inspection Readiness (Planning, Preparation and Close Out) • Support for U.S. New Drug Application, Japanese New Drug Application and European Marketing Authorization Application Submission • Data Management • Technical Writing • Creation of Standard Operation Procedures and Work Practices • Creation of Manuals and Project Specific Plans and Tools • Provide Educational Service to Individuals and Organizations Administrative Medical Services • Medical Informatics • Medical Coding • General Medical Administrative Support • Review of Medical Documents • General Administrative Medical Services Other Services • Review of Regulatory Documents • Review of Responses to Request for Proposal, Contracts for Clinical Trial and Strategic Partners • Investigator Grant Review • Medical Software Testing • Pharmaceutical Software Testing

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$80/hr Ongoing

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LAH Clinical is a Consulting Research Organization that provides clinical research, administrative, medical and scientific services to pharmaceutical and biotechnology companies, private organizations, Government agencies, Non-Governmental Organizations (NGOs), Medical Institutions and other similar industries. LAH Clinical provides the following clinical, administrative, and medical services to its clients: Clinical Research Services • Clinical Research Management of Phase I through 4 Clinical Trials • Clinical Project Management • Trial Master File (TMF) Development, Set-up, Maintenance and Management • Clinical Document Management • Drug Master File (DMF) • Inspection Readiness (Planning, Preparation and Close Out) • Support for U.S. New Drug Application, Japanese New Drug Application and European Marketing Authorization Application Submission • Data Management • Technical Writing • Creation of Standard Operation Procedures and Work Practices • Creation of Manuals and Project Specific Plans and Tools • Provide Educational Service to Individuals and Organizations Administrative Medical Services • Medical Informatics • Medical Coding • General Medical Administrative Support • Review of Medical Documents • General Administrative Medical Services Other Services • Review of Regulatory Documents • Review of Responses to Request for Proposal, Contracts for Clinical Trial and Strategic Partners • Investigator Grant Review • Medical Software Testing • Pharmaceutical Software Testing

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