Non Executive Director
Current
Nov 2023 - Present
AeroLeads people directory · profile
Daphne Sawlwin Email & Phone Number
Non Executive Director
at
LiverWELL
1 work email found
@csl.com.au
LinkedIn matched
✓ Verified July 2026
4 data sources
Profile completeness 100%
Who is Daphne Sawlwin? Overview
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Quick answer
Daphne Sawlwin is listed as Non Executive Director at LiverWELL, based in Greater Melbourne Area, Australia. AeroLeads shows a work email signal at csl.com.au and a matched LinkedIn profile for Daphne Sawlwin.
Daphne Sawlwin previously worked as Therapeutic Area Head, Vaccines at Csl Seqirus and Therapeutic Area Head, Vaccines at Csl Limited. Daphne Sawlwin holds Graduate from Australian Institute Of Company Directors.
Company email context
Email format at LiverWELL
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{first}.{last}@csl.com.au
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Profile bio
About Daphne Sawlwin
Medically qualified executive leader with extensive experience and expertise in pharmaceutical clinical research, clinical development, and safety risk management in many therapeutic areas. Demonstrated success in building and leading diverse, high-performance physician and scientific teams to strive for excellence. Enduring passion for safe & effective use of medicinal products, patient-centered systems of care, equitable access to medicines and quality health systems for all, and community service. Current responsibilities include board directorship, Therapeutic Area Head and Capability Uplift for medical team.
Listed skills include Clinical Research, Clinical Trials, Risk Management, Clinical Monitoring, and 11 others.
Current workplace
Daphne Sawlwin's current company
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8 roles
Daphne Sawlwin work experience
A career timeline built from the work history available for this profile.
Therapeutic Area Head, Vaccines
Csl Seqirus
Therapeutic Area Head, Vaccines
Csl Limited
Jul 2014 - Jun 2016
Head, Safety And Pharmacovigilance
Established a new clinical safety and pharmacovigilance (PV) group for bioCSL. Established the procedure and processes for a new pharmacovigilance system, management of the entire department, and implementation of the the PV system that is compliant with the new EU pharmavigilance legislation, Good Vigilance Practices.
Feb 2013 - Jun 2014
Director, Regions, Asia Pacific
Csl Australia Pty Limited
The Australian QPPV (Qualified Person for Pharmacovigilance) interacting with the Therapeutic Goods Administration in Australia. As the Director Regions, Asia Pacific, acted as a subject matter expert and liaison person for Quality/GMP for early safety signal detection and risk management relating to product quality defects. Provided leadership and training to Local and Regional Safety Offers (LSO/RSO) within commercial operations in Regional Offices (Hong Kong, Japan and New Zealand) for audit preparation, inspection readiness and for pharmacovigilance regulatory compliance.
May 2012 - Jan 2013
Clinical Safety Physician/Director- Clinical Safety
Responsible for providing input into the safety section of the protocols, evaluation/interpretation of clinical safety data arising from the various clinical development programs in the therapeutic area of vaccine, onology and plasma-derived products. Developed strategy and led preparation of entire clinical safety section for biological licence application (product registration) as well as developing the company core safety data sheet (CCSI) and product labels. Experienced in developing the strategies for integrated summary of safety (ISS). Oversees life cycle safety risk management activities including signal detection, signal evaluation/validation, periodic risk benefit evaluation, risk mitigation and effectiveness of risk mitigation measures. Responsible for line management of Clincical Safety Scientists between Sept 2010 to August 2011.
Oct 2007 - Apr 2012
Medical Director/Project Director/Clinical Project Leader
Omnicare Clinical Research
Provided clinical development strategies for biotech clients. Acquired in-depth knowledge of drug development as a result of experience in clinical trials from phase I to IV involving many indications in a wide ranging therapeutic areas. Provided medical monitoring support to many clinical studies in the Asia Pacific region as well as therapeutic area training for clinical monitoring staff. Therapeutic areas expertise include intensive care, oncology (early and late phase studies), hormone replacement therapies, and clinical psychiatry (depression and biopolar disorders).
Jul 2002 - Oct 2007
Contractor For Clinical And Medical Monitoring Work
Wyeth Pharmaceuticals, Aventis Paster And Polartechnic
Apr 1999 - Jun 2002
5 education records
Daphne Sawlwin education
Master In Clinical Epidemiology, Clinical Epidemiology/Clinical Research Method
Graduate Certificate In Evidence-Based Practice, Evidence-Based Medicine
Bachelor Of Medical Science, Immunology, Honours
Newcastle University, Australia
Bachelor Of Medicine, Bachelor Of Surgery (M.B.B.S.), General Medicine
Medical School, Rangoon, Burma
FAQ
Frequently asked questions about Daphne Sawlwin
Quick answers generated from the profile data available on this page.
What company does Daphne Sawlwin work for?
Daphne Sawlwin works for LiverWELL.
What is Daphne Sawlwin's role at LiverWELL?
Daphne Sawlwin is listed as Non Executive Director at LiverWELL.
What is Daphne Sawlwin's email address?
AeroLeads has found 1 work email signal at @csl.com.au for Daphne Sawlwin at LiverWELL.
Where is Daphne Sawlwin based?
Daphne Sawlwin is based in Greater Melbourne Area, Australia while working with LiverWELL.
What companies has Daphne Sawlwin worked for?
Daphne Sawlwin has worked for Liverwell, Csl Seqirus, Csl Limited, Biocsl, A Division Of Csl Limited, and Csl Australia Pty Limited.
How can I contact Daphne Sawlwin?
You can use AeroLeads to view verified contact signals for Daphne Sawlwin at LiverWELL, including work email, phone, and LinkedIn data when available.
What schools did Daphne Sawlwin attend?
Daphne Sawlwin holds Graduate from Australian Institute Of Company Directors.
What skills is Daphne Sawlwin known for?
Daphne Sawlwin is listed with skills including Clinical Research, Clinical Trials, Risk Management, Clinical Monitoring, Oncology, Gcp, Regulatory Affairs, and Clinical Development.
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