Robert Vanderpool Email and Phone Number

I am currently looking for a new opportunity for employment in Clinical Research. I am looking for a position with a company that has room for advancement.

Responsibilities include management of study sites, conduct pre-investigational site visits, study initiation visits, routine monitoring visits and study close-out visits in accordance with corporate, sponsor, FDA and ICH guidelines. Provide site orientation and guidance to assure successful performance of study protocol; review source documents and case report forms in compliance with stated guidelines; assure completion, submission and maintenance of regulatory documents. Prepare and timely submit accurate monitoring reports and manage regional home office.

Responsibilities include management of study sites, conduct pre-investigational site visits, study initiation visits, routine monitoring visits and study close-out visits in accordance with corporate, sponsor, FDA and ICH guidelines. Provide site orientation and guidance to assure successful performance of study protocol; review source documents and case report forms in compliance with stated guidelines; assure completion, submission and maintenance of regulatory documents. Prepare and timely submit accurate monitoring reports and manage regional home office.

Responsibilities include management of study sites, conduct pre-investigational site visits, study initiation visits, routine monitoring visits and study close-out visits in accordance with corporate, sponsor, FDA and ICH guidelines. Provide site orientation and guidance to assure successful performance of study protocol; review source documents and case report forms in compliance with stated guidelines; assure completion, submission and maintenance of regulatory documents. Prepare and timely submit accurate monitoring reports and manage regional home office.

Responsibilities include management of 60 resident wing in a 285 bed state long term care facility for veterans. Supervise forty nursing assistants and fifteen nurses to ensure that the veterans served are appropriately taken care of. Responsible for managing budget for the unit to ensure fiscal compliance.

Responsibilities include management of study sites, conduct pre-investigational site visits, study initiation visits, routine monitoring visits and study close-out visits in accordance with corporate, sponsor, FDA and ICH guidelines. Provide site orientation and guidance to assure successful performance of study protocol; review source documents and case report forms in compliance with stated guidelines; assure completion, submission and maintenance of regulatory documents. Prepare and timely submit accurate monitoring reports and manage regional home office.

Responsibilities include management of study sites, conduct pre-investigational site visits, study initiation visits, routine monitoring visits and study close-out visits in accordance with corporate, sponsor, FDA and ICH guidelines. Provide site orientation and guidance to assure successful performance of study protocol; review source documents and case report forms in compliance with stated guidelines; assure completion, submission and maintenance of regulatory documents. Prepare and timely submit accurate monitoring reports and manage regional home office. Provide guidance and training for peers and inexperienced Clinical Research Associates. Prepare and timely submit accurate monitoring reports, manage regional home office and manage business affairs of LLC. Providing contract CRA duties for such CRO’s and Sponsors as: Paragon Biomedical, Premier Research Group, Xenoport, Shire and I3 Research.

Responsibilities include management of study sites, conduct pre-investigational site visits, study initiation visits, routine monitoring visits and study close-out visits in accordance with corporate, sponsor, FDA and ICH guidelines. Provide site orientation and guidance to assure successful performance of study protocol; review source documents and case report forms in compliance with stated guidelines; assure completion, submission and maintenance of regulatory documents. Prepare and timely submit accurate monitoring reports and manage regional home office

Responsibilities include management of study sites, conduct pre-investigational site visits, study initiation visits, routine monitoring visits and study close-out visits in accordance with corporate, sponsor, FDA and ICH guidelines. Provide site orientation and guidance to assure successful performance of study protocol; review source documents and case report forms in compliance with stated guidelines; assure completion, submission and maintenance of regulatory documents. Provide guidance and training for peers and inexperienced Clinical Research Associates. Prepare and timely submit accurate monitoring reports, manage regional home office and manage business affairs of LLC. Providing contract CRA duties for such CRO’s and Sponsors as: Eli Lilly and Co., Kendle International, Isis Pharmaceuticals, Merck and Paragon Biomedical.

Responsibilities include management of study sites, conduct pre-investigational site visits, study initiation visits, routine monitoring visits and study close-out visits in accordance with corporate, sponsor, FDA and ICH guidelines. Provide site orientation and guidance to assure successful performance of study protocol; review source documents and case report forms in compliance with stated guidelines; assure completion, submission and maintenance of regulatory documents. Prepare and timely submit accurate monitoring reports and manage regional home office.

Responsibilities include management of study sites, conduct pre-investigational site visits, study initiation visits, routine monitoring visits and study close-out visits in accordance with corporate, sponsor, FDA and ICH guidelines. Provide site orientation and guidance to assure successful performance of study protocol; review source documents and case report forms in compliance with stated guidelines; assure completion, submission and maintenance of regulatory documents. Prepare and timely submit accurate monitoring reports and manage regional home office.

Responsibilities include management of study sites, conduct pre-investigational site visits, study initiation visits, routine monitoring visits and study close-out visits in accordance with corporate, sponsor, FDA and ICH guidelines. Provide site orientation and guidance to assure successful performance of study protocol; review source documents and case report forms in compliance with stated guidelines; assure completion, submission and maintenance of regulatory documents. Prepare and timely submit accurate monitoring reports and manage regional home office.

Research Coordinator for numerous pharmaceutical research studies and grants focusing on Infectious diseases. Responsible for all data collection and maintenance, investigational drug inventory, case report form completion and submission, prepare submissions for IRB review and all other aspects of study administration. Studies involved with included numerous HIV, Kaposi ’s sarcoma, pneumonia, bronchitis, soft tissue infections and Enteroviral Aseptic Meningitis.