Adnan Dahdul, M.D. serves as Medical Director and President. Dr. Dahdul has extensive experience conducting clinical research and oversees a team of dedicated, well-trained health care professionals.
FutureCare Studies' staff includes a full-time nurse practitioner, sub-investigator; certified clinical research coordinators, registered nurses, research assistants, as well as a regulatory specialist who oversees the procurement and submissions of regulatory documents.
Adnan Dahdul, MD, Medical Director - board certified in Internal Medicine and has been the Principal Investigator for over 90 clinical research trials since 1996. Dr. Dahdul is very well versed in his role as Principal Investigator, as well as ICH and GCP guidelines.
Tammy Colby, Director of Business Operations - Tammy oversees budget expenditures and provides direction and structure for administrative support functions, including clerical support, mail services, purchasing, office assignments, and contracts for outside services.
Laurie Bourgelas, PA-C, Sub-Investigator
Annette Scarnici, RN, CCRC, Clinical Research Coordinator
Heather Herbert, RN, CCRC, Clinical Research Coordinator
Rosa Torres, Research Assistant
Angel Colby, Regulatory Affairs Specialist
Kathy Cossaboom, Administrative Assistant
Clinical Research Coordinator (general responsibilities):
Manages all aspects of conducting clinical trials. The research coordinator is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As the primary resource for the protocols, the clinical research coordinator will act as liaison between the investigators, primary care providers and the sponsor. Along with the investigator, the clinical research coordinator will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, the nurse/coordinator is responsible for all data and source documentation, adverse experience reporting, and end of study reporting.
Research Assistant (general responsibilities):
Assists the Clinical Research Coordinator in conducting the clinical trial. The research assistant is responsible for collecting, processing, storing and handling clinical specimens, scheduling study patients for follow-up, and collecting, recording and filing clinical data. |
