Advance Research Center LLC

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Staff

  • Board Certified Medical Doctor.
  • Nurse Practitioners
  • Nurse Coordinators
  • Coordinators
  • EDC Department
  • QC Department
  • Regulatory Department
  • Pharmacist Coordinator
  • Phlebotomist coordinator

CEO: Yovanny Blanco, CRC

Specialized research professional working with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilities, and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works with the PI, department, sponsor, and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.

Clinical SITE DIRECTOR: NAILAN ESTRADA FMG, ASN, CRC, Regulatory Affairs.

Specialized research professional working with and under the direction of the clinical Principal Investigator (PI). Supports, facilitates and coordinates the daily activities of the clinical trial and plays a fundamental role in the conduct of the study,

Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to)  protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training.

Collaborates with PI and institution to respond to any audit findings and implement approved recommendations.

Foreign Doctor in Medicine with 16 years of experience in the Medical Field.

Anthony Ferrer, CRC

Coordinates with Principal Investigator to help ensure that clinical research and related activities are performed in accordance with federal regulations and university and sponsoring agency policies and procedures.

Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to)  protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training.

Assists Principal Investigator to assure that all key personnel or persons ‘engaged’ in the research project have met training requirements in accordance with federal regulations and university and sponsoring agency policies and procedures.

Cooperates with university compliance and monitoring efforts related to sponsored program administration and reports instances of noncompliance to the appropriate compliance office. Coordinates and facilitates monitoring and auditing visits. Notifies appropriate institutional officials of external audits by FDA and sponsors.

Melanie Blanco, CRC

Coordinates with Principal Investigator to help ensure that clinical research and related activities are performed in accordance with federal regulations and university and sponsoring agency policies and procedures.

Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to)  protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training.

Assists Principal Investigator to assure that all key personnel or persons ‘engaged’ in the research project have met training requirements in accordance with federal regulations and university and sponsoring agency policies and procedures.

Cooperates with university compliance and monitoring efforts related to sponsored program administration and reports instances of noncompliance to the appropriate compliance office. Coordinates and facilitates monitoring and auditing visits. Notifies appropriate institutional officials of external audits by FDA and sponsors

Marianne Blanco, CRC

Coordinates with Principal Investigator to help ensure that clinical research and related activities are performed in accordance with federal regulations and university and sponsoring agency policies and procedures.

Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to)  protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training.

Assists Principal Investigator to assure that all key personnel or persons ‘engaged’ in the research project have met training requirements in accordance with federal regulations and university and sponsoring agency policies and procedures.

Cooperates with university compliance and monitoring efforts related to sponsored program administration and reports instances of noncompliance to the appropriate compliance office. Coordinates and facilitates monitoring and auditing visits. Notifies appropriate institutional officials of external audits by FDA and sponsors.

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