Cecilia Chia Email & Phone Number | Qualified Pharmacist and PhD with >10 years’ experience in clinical research range of activities includes safety management, trial monitoring, project management and Quality Assurance. Experience in international marketing and NDA studies, and 7 years experience working in pharmacovigilance functions. In Genzyme build and lead the PV and Medical Affairs functions in the AsiaPacific region. Set up PV teams in the countries, developed necessary SOPs and maintain reporting requirements according to country’s regulations. Assess and maximize use of available resources. Work cross functionally with regulatory and clinical research, locally and with global teams to ensure compliance. As AstraZeneca’s GCP manager for Asia, developed and implemented programs of high quality standards to adhere to GCP. Conducted QC reviews for trials for audits and inspections. Promoted Asia as a site for NDA trials as Clinical Project Manager for the region. Was instrumental in convincing HQ to include Asia in Astra’s NDA studies. Able to successfully run a NDA study in Vietnam, a first in the industry. As Regional Training Manager for Quintiles, conducted technical training for CRAs and soft skills training for all staff in the SEA region. Evaluated training needs of staff,developmental needs for managers, and organizational development. As QA auditor, I conducted audits on drug supply facilities, a pharmacovigilance department and trial sites in various parts of Asia. At Takeda, I am responsible for setting up the PV systems within clinical development programs to ensure compliance to regulatory requirements. Part of different global groups and safety teams representing Asia. I moved to QA to oversee the local commercial offices in PV, GCP and Quality Management systems. In Merck biopharma, I head up the APAC region including Japan and China. Specialties: Pharmacovigilance, Medical Affairs, clinical research, Training

Cecilia Chia

Qualified Pharmacist and PhD with >10 years’ experience in clinical research range of activities in...
Singapore

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Cecilia Chia’s Email ccliachia@yahoo.com.sg

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Cecilia Chia’s Location Singapore

Cecilia Chia’s Current Industry Merck Group Biopharma

Cecilia Chia’s Prior Industry Takeda | Takeda Global Research And Development | Genzyme | Quintiles East Asia

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Work Experience

Merck Group Biopharma

Head Of Global Patient Safety Asia Pacific

2014-04-01 00:00:00 - Present

Takeda

Director, Qa Support For Local Companies Pv And Gcp

2012-10-01 00:00:00 - 2014-03-01 00:00:00

Takeda Global Research And Development

Associate Director, Pharmacovigilance

2011-09-01 00:00:00 - 2013-10-01 00:00:00

Genzyme

Senior Medical Affairs Manager

2006-10-01 00:00:00 - 2011-09-01 00:00:00

Quintiles East Asia

Quality Assurance Auditor

2005-06-01 00:00:00 - 2006-09-01 00:00:00

Skills

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Languages

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FAQ About Cecilia Chia

Cecilia Chia is located at
Singapore

Cecilia Chia is a Qualified Pharmacist and PhD with >10 years’ experience in clinical research range of activities includes safety management, trial monitoring, project management and Quality Assurance. Experience in international marketing and NDA studies, and 7 years experience working in pharmacovigilance functions. In Genzyme build and lead the PV and Medical Affairs functions in the AsiaPacific region. Set up PV teams in the countries, developed necessary SOPs and maintain reporting requirements according to country’s regulations. Assess and maximize use of available resources. Work cross functionally with regulatory and clinical research, locally and with global teams to ensure compliance. As AstraZeneca’s GCP manager for Asia, developed and implemented programs of high quality standards to adhere to GCP. Conducted QC reviews for trials for audits and inspections. Promoted Asia as a site for NDA trials as Clinical Project Manager for the region. Was instrumental in convincing HQ to include Asia in Astra’s NDA studies. Able to successfully run a NDA study in Vietnam, a first in the industry. As Regional Training Manager for Quintiles, conducted technical training for CRAs and soft skills training for all staff in the SEA region. Evaluated training needs of staff,developmental needs for managers, and organizational development. As QA auditor, I conducted audits on drug supply facilities, a pharmacovigilance department and trial sites in various parts of Asia. At Takeda, I am responsible for setting up the PV systems within clinical development programs to ensure compliance to regulatory requirements. Part of different global groups and safety teams representing Asia. I moved to QA to oversee the local commercial offices in PV, GCP and Quality Management systems. In Merck biopharma, I head up the APAC region including Japan and China. Specialties: Pharmacovigilance, Medical Affairs, clinical research, Training

Cecilia Chia currently works in the Merck Group Biopharma |

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Cecilia Chia has prior
experience in the following industries:
Takeda | Takeda Global Research And Development | Genzyme | Quintiles East Asia

Cecilia Chia has the following professional experience:
Merck Group Biopharma | Takeda | Takeda Global Research And Development | Genzyme | Quintiles East Asia