Ben Blaylock Email & Phone Number

Ben Blaylock has worked with Hart Clinical Consultants as a senior clinical research consultant since 2012. In this role, Ben serves as case proctor, clinical site manager and study monitor for high profile clients such as Intersect ENT and Stryker Neurovascular.

Pracs Institute (Formerly Cetero Research)

Supervises and manages all aspects of clinical operations for outpatient trials. Provides leadership, organization, supervision and direction by collaborating with all areas of practice including clinical, as well as non-clinical areas to ensure all research activities comply with company policies and regulatory guidelines (FDA, EU, and Canadian). Assists with the development and implementation of strategic initiatives for process improvements, business development, client management, SOP development, and compliance-related processes. Initiates collaboration with other Associate Directors and Managers within Clinical Operations and Integrated Services to assist with the management/coordination of services in maintaining department functions at a performance level equal or superior to required standards, regulatory guidelines, and client expectations.Maintains a comprehensive and in-depth understanding of all clinical operations, providing recommendations for operational and process improvements.Responsible for working with existing resources to resolve individual department issues including staffing levels, differences of opinion over policies & SOP’s as well as taking appropriate disciplinary action in accordance with company policies.

Cetero Research (Formerly Dgd Research)

Employed as an RN, CRC managing endocrine related research trials. Coordinator experience on over 45 clinical trials, including phase I-IV drug and device trials, including insulin pumps and implantable devices. Experience also included 5 years of extensive diabetes education with type 1 and type 2 diabetics. During tenure as a CRC, acquired CCRC (certified clinical research coordinator) accreditation from the ACRP in June 2009. Responsibilities include: overseeing research assistants, CRC IIs, as well as a collaborative effort with regulatory personnel, lab technicians, as well as other ancillary staff to manage patient visits and coordinate trial according to protocol and GCP guidelines; involved with preparation of regulatory documents, facilitating communication with regulatory department and Central vs Local IRBs; preparation and management of source documentation and responsible for data transcription to CRF/e-CRFs; experienced with recruitment, retention, eligibility screening/pre-screening of qualified subjects for clinical trials; dispensing of trial medications; adverse event reporting; safety reporting; query completion/resolution; and facilitating monitor visits along with sponsor and FDA audits.