Robin Bean Email & Phone Number | Clinical Research Professional with over 18 years experience. Diverse roles include study coordinator, regulatory specialist, in-house and regional CRA, and clinical trials manager. Successful implementation of global phase II and III clinical trials from study start up through FDA approval. Diligent and detail oriented problem solver with proven ability to multitask and execute projects independently according to established timelines. Demonstrated abilities include: - Operational Planning, Oversight and Execution of Projects - CRO, Vendor, and Site Management - Investigator Meeting Planning and Presentation - Clinical Research Associate Training and Co-Monitoring - Informed Consent Development, Review and Negotiation - Case Report Form (CRF) Development and Completion - Study Document Development (Tools, Templates, and Guidelines) - Site Monitoring Visits (Site Qualification, Initiation, Monitoring, Close-out) - Regulatory Document Management and Review - Local and Central IRB submission - Audit Preparation, Completion and Follow-up

Robin Bean

Clinical Research Professional with over 18 years experience. Diverse roles include study coordinat...
176 South 45th Avenue, Brighton, United States

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Robin Bean’s Email robin.bean@vrtx.com

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Robin Bean’s Location 176 South 45th Avenue, Brighton, United States

Robin Bean’s Current Industry Vertex Pharmaceuticals

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Site Activation Sr. Manager, Study Start-up and Amendments Teams

2017-01-01 00:00:00 - Present

Sr. Study Manager on assignment to Merck

2015-11-01 00:00:00 - 2016-11-01 00:00:00

Clinical Operations Manager

2012-06-01 00:00:00 - 2015-11-01 00:00:00

Clinical Research Regulatory Specialist

2010-07-01 00:00:00 - 2012-06-01 00:00:00

Clinical Trials Manager

2003-01-01 00:00:00 - 2009-01-01 00:00:00

Regional Clinical Research Associate

2001-01-01 00:00:00 - 2003-01-01 00:00:00

Study Coordinator

1998-01-01 00:00:00 - 2001-01-01 00:00:00

Registered Nurse

1996-01-01 00:00:00 - 1998-01-01 00:00:00

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Robin Bean is a Clinical Research Professional with over 18 years experience. Diverse roles include study coordinator, regulatory specialist, in-house and regional CRA, and clinical trials manager. Successful implementation of global phase II and III clinical trials from study start up through FDA approval. Diligent and detail oriented problem solver with proven ability to multitask and execute projects independently according to established timelines. Demonstrated abilities include: - Operational Planning, Oversight and Execution of Projects - CRO, Vendor, and Site Management - Investigator Meeting Planning and Presentation - Clinical Research Associate Training and Co-Monitoring - Informed Consent Development, Review and Negotiation - Case Report Form (CRF) Development and Completion - Study Document Development (Tools, Templates, and Guidelines) - Site Monitoring Visits (Site Qualification, Initiation, Monitoring, Close-out) - Regulatory Document Management and Review - Local and Central IRB submission - Audit Preparation, Completion and Follow-up

Robin Bean has prior
experience in the following industries:
Execupharm | Accera | National Jewish Health | Gilead Colorado | Pra International | Dallas Veterans Affairs Medical Center | Veterans Affairs Medical Center

Robin Bean has the following professional experience:
Vertex Pharmaceuticals | Execupharm | Accera | National Jewish Health | Gilead Colorado | Pra International | Dallas Veterans Affairs Medical Center | Veterans Affairs Medical Center