Clinical Research Data & Regulatory Coordinator occupation at Mary Bird Perkins Cancer Center in Baton Rouge

Mary Bird Perkins Cancer Center is currently seeking to employ Clinical Research Data & Regulatory Coordinator on Sat, 15 Jun 2013 03:42:06 GMT. DESCRIPTION Collaborates with the Clinical Research team and the Principal Investigator by knowledge of current protocol requirements; maintains IRB documents, regulatory and protocol documentation for assigned clinical trials administered by the Center which may include multi-site trials; facilitates communication and correspondence between Clinical Research and sponsoring agencies; collects...

Clinical Research Data & Regulatory Coordinator

Location: Baton Rouge Louisiana

Description: Mary Bird Perkins Cancer Center is currently seeking to employ Clinical Research Data & Regulatory Coordinator right now, this occupation will be placed in Louisiana. More details about this occupation opportunity kindly read the description below. DESCRIPTION

Collaborates with the Clinical Research team and the Principal Investigator by knowledge of current! protocol requirements; maintains IRB documents, regulatory and protocol documentation for assigned clinical trials administered by the Center which may include multi-site trials; facilitates communication and correspondence between Clinical Research and sponsoring agencies; collects protocol specific information from physicians, nurses, patients, family members, local caregivers, and others utilizing protocol specific methods; ensures that all designated Clinical Research regulatory and data management activities for all clinical research sites are executed in accordance with all applicable laws, regulations, policies and protocol requirements; performs additional duties as requested by supervisor and/or described in position description

DUTIES

Demonstrates knowledge & understanding of the evolution of Clinical ResearchParticipates in Clinical Research studies by assuring that the regulatory & data for trials are being managed according to riles & guideli! nes governing the conduict of clinical research trialsMonitor/! Auditor Preparation & ParticipationIRB Preparation & PresentationProtocol Research Document MaintenancePolicies & proceduresOther duties & professional development

QUALIFICATIONS

Education: Bachelor's degree or equivalent work experience, preferably in a scientific or technical disciplineBasic science degree or certification/licensure in a healthcare fieldQualifications: Clinical Research experience required*Oncology research experience preferredRegulatory experience with NCI trials & pharmaceutical sponsored trials required*Certification/Licensure: RN, LPN, and/or professional certifications preferred but not requiredSpecialized Knowledge: Thorough understanding of oncology terminology, cancer process, cancer treatment & prevention requiredGeneral computer knowledge & word processing Proficiency in Microsoft Office Demonstrates knowledge & understanding of the evolution of Clinical ResearchParticipates in Clinical Research studies by assuring that ! the regulatory & data for trials are being managed according to riles & guidelines governing the conduict of clinical research trialsMonitor/Auditor Preparation & ParticipationIRB Preparation & PresentationProtocol Research Document MaintenancePolicies & proceduresOther duties & professional development
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This occupation starts available on: Sat, 15 Jun 2013 03:42:06 GMT

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