Research Center Profile:
Center for Clinical Trials, LLC
Cardiology/Vascular Diseases
Dermatology
Endocrinology
Gastroenterology
Healthy Volunteers
Immunology
Infections and Infectious Diseases
Internal Medicine
Musculoskeletal
Nephrology
Neurology
Obstetrics/Gynecology (Women’s Health)
Oncology
Ophthalmology
Otolaryngology (Ear, Nose, Throat)
Pediatrics/Neonatology
Psychiatry/Psychology
Pulmonary/Respiratory Diseases
Rheumatology
Trauma (Emergency, Injury, Surgery)
Urology
Vaccines
Welcome to the Center for Clinical Trials, LLC, a center
dedicated to clinical research full time. This is the result of
over 20 years of collective experience in the fields of medicine
and clinical trials. This unique combination gives the site the
ability to effectively meet the needs of the sponsoring
companies.
Center for Clinical Trials, LLC is in partnership with USTCEDRES (University
of Santo Tomas Center for Drug Research, Evaluation and Studies), a
large clinical trial site in Manila, Philippines.
Center for Clinical Trials, LLC staff have worked with the
following pharmaceutical companies:
Abbott Laboratories, Alcon, Allergan, Astra-Zeneca, Bausch &
Lomb, Bayer, Biocryst, Bio-technology, Bristol Myers Squibb,
Glaxo-Smithkline, Merck, Pfizer, Proctor and Gamble, Roche,
RWJohnson, Sankyo Pharm, Sanofi-Aventis, Sanofi-Pasteur,
Schering-Plough, Tap Holdings, Hoechst Marion Roussel,
Viropharma..... and various CROs' such as Covance, CTMS,
DPClinical, I3 Research, Icon Clinical Research, MTRA, ORA,
Paragon, Parexel, Phoenix, PPD, pHARMACO, PRA, Quintiles, RSI, and
Topical Solution to name a few.
Our center does study phases II, III, and IV.
Center for Clinical Trials, LLC in Paramount boasts of a
research facility within the hospital community, with a total
footage of 2000 square feet solely dedicated to clinical research.
The center has the support of the hospital and medical-office
administrators in the medical community to send qualified subjects
to the research center. At present, CCT alone has 2,000 patient
database.
Our site is accessible from major thoroughfares. It is
approximately 20 miles east of LAX airport, 10 miles east of Long
Beach airport, and 30 miles north of John Wayne airport.
The center prides itself with board-certified/eligible
specialists dedicated and experienced in medical research. There
are 10 full-time experienced clinical research coordinators.
Investigators and coordinators alike have very focused approach in
conducting clinical trials, with adherence to Good Clinical
Practice principles cognizant of the FDA guidelines. The personnel
have published papers in popular scientific journals.
Eleuterio P. Delfin, Jr.M.D.
General Practice/Emergency Medicine
Jesse de Leon, M.D.
Ophthalmology
Liberation de Leon, M.D., F.A.A.P.
Pediatrics
Gregory J. Szal, M.D.
Otolaryngology
Mildred Rey, M.D.,F.A.A.P.
Pediatrics
Jesus Villanueva, M.D., A.B.I.M.
Internal Medicine
Jose Mari Elacion,M.D.
Family Practice
Ana R. Faitlowicz,M.D.
Oncology
Allan M. Effron,M.D.,FACG
Gastroenterology
Catalina Villanueva, M.D.
Director of Clinical Operations
Jonnel R. Constantino, M.D.
Subinvestigator
Ma. Victoria Constantino, M.D., MRA
Medical Research Assistant
Pebbles Hollero, M.D., CRC
Clinical Research Coordinator
Rey S. Chua, B.S., CRC
Clinical Research Coordinator
Gloria D. Libunao, B.S., CRC
Cora D. Diocampo, B.S., LLB
Clinical Research Coordinator
Caroline Villanueva,B.S., CRC
Clinical Research Coordinator
Isa V. Chua, B.S., CRC
Administrator/Regulatory Coordinator
Domingo S. Caparas,Jr,M.D.
Medical Research Associate
Angelica Samarista-Giron,M.D.,BSN
Clinical Research Coordinator,Phil
Mark R. David,M.D.
Clinical Research Coordinator,Phil
Melody Espino,M.D.
Clinical Research Coordinator,Phil.
NOTICE OF JOB OPPORTUNITY
MEDICAL RESEARCH ASSOCIATE:
Conduct Research and clinical investigation during clinical trials pertaining to safety and effects of medications. No patient treatment involved. Review and analyze professional, scientific & medical journals regarding health issues and developments relevant to patient illness and history in order to recommend possible tests or procedures that may be relevant to diagnosis needed during clinical trials. Review laboratory results, recognize and monitor parameters that may be clinically significant, highlight and present results for further review and assessment. Participate in meeting and conferences held by pharmaceutical and other research companies before commencement of any research projects. Provide assistance to ensure protocol is followed throughout clinical study.
Requirements:
Doctor of Medicine or Life Sciences. No license required. 40 hours/week. Jobsite/Interview: Paramount, CA. Contact information: Mail resume to: Center for Clinical Trials, LLC. - 16660 Paramount Blvd., #301, Paramount, CA 90723. Attn: Director
Center for Clinical Trials,LLC is an independent research
facility. It utilizes central IRB and central laboratory with
access to reputable local laboratory and diagnostic centers. It has
an access to a large computerized database of patients with varied
ages, ethnicity, socioeconomic strata and medical conditions that
ensure a stable source of patient population and guarantees to meet
the minimum numbers of subjects as was proven in the past.
- 40% Hispanics
- 45% Caucasians
- 15% Asians
- 5% Others
If you are interested in contacting this center to discuss placing a clinical
trial there, please complete and send the email form below. A representative from
the research center will then follow up with you.
