Fernando Caday
* ******* ****, #***, **** Lee, NJ 07024
Phone: 201-***-**** . Email: ******@***.***
OBJECTIVE:
A challenging position in clinical trials arena with the opportunity for growth.
QUALIFICATIONS:
Certified Clinical Research Professional, Society of Clinical Research Associates
Dedicated professional with excellent background in life sciences
Extensive training and knowledge of Human Subject Protection and GCP/ICH
Highly motivated, organized, hardworking and works well both independently and
collaboratively in a team setting.
Fluency in oral and written communication
Adept computer knowledge and experience.
WORK HISTORY:
Clinical Research Coordinator
Mount Sinai Hospital – Mount Sinai School of Medicine
New York, New York
June, 2009 – Present
Manage and maintain the research study databases
Create queries and generate reports on the research project database
Prepare documents for IRB submission and ma intain regulatory binders
Coordinate the clinical assessments of study subjects including screening and
recruitment
Obtain informed consent and educate participants about research study concepts
and details
Schedule subject participants’ visit and subsequent follow-ups
Perform data collection and maintain source documents and subject files
Assist in study protocol modification and amendments
Assist in creating meeting agenda and maintain meeting minutes
Provide assistance in mentoring other research coordinators in training
Clinical Program Coordinator
Jewish Home & Hospital Community Services Division, New York City, NY
December, 2007 – December, 2008
Organized and coordinated the Psychiatric and Palliative Care
Consultation Services.
Assisted in writing grant proposal and in other aspects of research projects.
Created reports, presentation, and assisted in data evaluation.
Operations Manager
The Church of the Holy Innocents, New York City, NY
September 1995-October 2007
● Responsible for the daily operations of the church and rectory
office, including human resources and office management.
Dental Assistant
Dental Arts, Hoboken NJ
January 1995 – August 1995
Dental Office of Dr. Perry Yap, Los Angeles, CA
January 1994 – December 1994
Assisted in new patient evaluation and comprehensive examination and in all basic
restorative and supportive dental procedures
Dental Associate
Concepcion Polyclinic, Marikina Philippines
November 1991- October 1993, May 1985 – May 1988
Practiced all aspects of general dentistry with two other practitioners
Seminarian
Society of Jesus, Ateneo de Manila University, Philippines
June 1988 – October 1991
TRAINING:
Clinical Research Volunteer
Mount Sinai Hospital – Mount Sinai School of Medicine
New York, New York
February, 2009 – May 2009
Assisted in recruitment and follow up of clinical study participants
Prepared clinical study binders, documents and distribute d study fliers
Assisted in all other organizational aspects of clinical studies
Pathways in Clinical Research Associates and
Clinical Research Coordinator, Certificate, 2006
Rutgers the State University College of Nursing
Newark, New Jersey
Drug development and protocol design
GCP and study conduct, safety monitoring and adverse events reporting
Regulatory requirements and ethical issues
Extensive ICH GCP training
Clinical site monitoring (site selection, initiation, monitoring and close out )
EDUCATION/CERTIFICATION:
Doctor of Dental Medicine, 1984
University of the East College of Dentistry
Quezon City, Philippines
Certified Clinical Research Professional, 2011
Society of Clinical Research Associates
U.S.A.
Seminary Studies, 1988-1991
Ateneo de Manila University
Quezon City, Philippines
REFERENCES: Available upon request.