Carla Lopez Email & Phone Number | Senior Clinical Research Associate with 12 years clinical monitoring experience. As a CRA, handled Phase 2 and Phase 3 studies on Vaccine, Infectious Diseases, SLE, Diabetes with Dyslipidemia and Hypertension, Gastric and Duodenal Ulcers and Rheumatoid Arthritis. Performed onsite and remote Site Selection visits for Phase 2 and Phase 3 studies on Oncology, Vaccine, SLE, Infectious Diseases, Gastrointestinal, Rheumatoid Arthritis therapeutics. Performed onsite and remote Site Initiation and interim visits for Phase 2 and Phase 3 studies on Vaccine, Lupus Nephritis, Infectious Diseases, Gastric Ulcer, Duodenal Ulcer and DM studies. Moreover, completed onsite and remote Closeout visit for Vaccine, Lupus Nephritis, Infectious Diseases, Gastric Ulcer, Duodenal Ulcer and DM studies. In addition, performed remote pre-study visit for US sites and remote monitoring visit for Phase 3 Respiratory vaccine study in U.S sites (with valid US visa). As CRA, worked as unblinded for Flu vaccine and Lupus Nephritis studies. Performed 100% and reduced SDV. Trained on Risk Based Monitoring. Trained on therapeutics and monitoring on Oncology, Infectious Diseases, Gastric and Duodenal ulcers, DM and vaccine studies. Furthermore, as CRA 1, lead in the preparation, during and post- local and US FDA inspection for vaccine study. In addition, as CRA, have experience in clinical systems like CTMS, RAVE EDC and RTSM, Inform, Cenduit, IWRS/IVRS, Veeva Vault, secure consent, CRIO, Florence and Complion As Clinical Trial Assistant for 4 years, provided support in Trial Master File (TMF), study supplies, safety letter distribution and tracking, updating of clinical systems and site payment management. In addition, as CTA, maintains in-house files, updating clinical systems like CTMS, informatics and other external project related systems

Carla Lopez

Senior Clinical Research Associate with 12 years clinical monitoring experience. As a CRA, handled...
Manila, Manila, Philippines

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Work Experience

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Senior Clinical Research Associate

2021-08-01 00:00:00 - Present

Ppd

Senior Clinical Research Associate

2020-11-01 00:00:00 - 2021-08-01 00:00:00

Iqvia Rds

Clinical Research Associate

2010-10-01 00:00:00 - 2020-11-01 00:00:00

Iqvia

Clinical Research Associate

2014-01-01 00:00:00 - 2020-11-01 00:00:00

Iqvia Asia Pacific

Clinical Research Associate I

2014-01-01 00:00:00 - 2019-07-01 00:00:00

Quintiles

Clinical Research Associate Trainee

2014-01-01 00:00:00 - 2014-07-01 00:00:00

Pfizer

Cme For International Conventions

2009-03-01 00:00:00 - 2010-10-01 00:00:00

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FAQ About Carla Lopez

Carla Lopez is located at
Manila, Manila, Philippines

Carla Lopez is a Senior Clinical Research Associate with 12 years clinical monitoring experience. As a CRA, handled Phase 2 and Phase 3 studies on Vaccine, Infectious Diseases, SLE, Diabetes with Dyslipidemia and Hypertension, Gastric and Duodenal Ulcers and Rheumatoid Arthritis. Performed onsite and remote Site Selection visits for Phase 2 and Phase 3 studies on Oncology, Vaccine, SLE, Infectious Diseases, Gastrointestinal, Rheumatoid Arthritis therapeutics. Performed onsite and remote Site Initiation and interim visits for Phase 2 and Phase 3 studies on Vaccine, Lupus Nephritis, Infectious Diseases, Gastric Ulcer, Duodenal Ulcer and DM studies. Moreover, completed onsite and remote Closeout visit for Vaccine, Lupus Nephritis, Infectious Diseases, Gastric Ulcer, Duodenal Ulcer and DM studies. In addition, performed remote pre-study visit for US sites and remote monitoring visit for Phase 3 Respiratory vaccine study in U.S sites (with valid US visa). As CRA, worked as unblinded for Flu vaccine and Lupus Nephritis studies. Performed 100% and reduced SDV. Trained on Risk Based Monitoring. Trained on therapeutics and monitoring on Oncology, Infectious Diseases, Gastric and Duodenal ulcers, DM and vaccine studies. Furthermore, as CRA 1, lead in the preparation, during and post- local and US FDA inspection for vaccine study. In addition, as CRA, have experience in clinical systems like CTMS, RAVE EDC and RTSM, Inform, Cenduit, IWRS/IVRS, Veeva Vault, secure consent, CRIO, Florence and Complion As Clinical Trial Assistant for 4 years, provided support in Trial Master File (TMF), study supplies, safety letter distribution and tracking, updating of clinical systems and site payment management. In addition, as CTA, maintains in-house files, updating clinical systems like CTMS, informatics and other external project related systems