Every single one of our clients wants to work with us on their next study.

With over 30 years’ experience within multi-national pharmaceutical and CRO industries and an extensive background in regulatory and clinical trials, Jacquie has a holistic understanding of all aspects of drug development. 

More recently as Managing Director, Jacquie has grown PharmaSols to be an extremely successful Australia and New Zealand focused CRO. Building a culture of expertise through a supportive environment, quality focus and overall collaboration and trust – both internally and externally.

With 15 years of experience across the academic, translational research and CRO spaces, Sam is focused on working closely with emerging pharma and biotech companies at the critical early stages of trial development in Australia & New Zealand.

Based in Sydney, Australia, with a keen interest in the Asia-Pacific region, and a long track record in enabling drug and device studies across the region, Sam is the conduit between the business, operational and service delivery teams for our clients. 

Elaine brings with her over 25 years of experience working in a variety of roles within the clinical trial and contract research industry both internationally and locally within the multi-national pharmaceutical and the CRO environment.

With her strong operational and management expertise, she oversees all project deliverables and supports, mentors, and develops her project management team and other staff throughout the organisation to ensure we meet our clients' clients project deliverables.

Fiona has worked for over 20 years for a variety of large and small CRO's, Biotech and Pharma companies. Roles have been predominantly in Clinical Operations across AsiaPac, managing operational teams and projects. Additionally, she has also worked in Business Development, working to find the best clinical trial strategy for clients. She has a strong focus on developing the team, promoting high quality team-work and deliverables for clients.​

Jorrit has worked over 20 years in clinical research in AsiaPac and Europe for Pharmaceutical companies, CRO's and Central Laboratories.  His experience includes clinical operations, project management and quality assurance both at management and operations levels.​

Jorrit oversees the delivery of all study start up activities completed by his team of regulatory and clinical experts, from document development, submissions, site contracts and file set up. Jorrit's team also supports the operations team for ongoing ethics and health authority reporting after clinical trial commencement.

Nicole has 25 years’ experience in leadership and strategy development from within the Finance Team of small businesses. 

Her widely recognised commercial judgement, visionary thinking, emotional intelligence and constructive leadership style, inspires teams to deliver quality results.

A versatile regulatory specialist with nearly 20 years history of working in the pharmaceutical industry, Terri is skilled in pharmaceuticals, clinical trials, regulatory requirements, compliance and licensing and has a MPharm (Hons) focused in Pharmacy.

She has experience with regulatory requirements and submissions for both New Zealand and Australia and previously for South East Asia.

Marina has worked in clinical research for over 22 years and comes with diverse clinical experiences in oncology, haematology, paediatrics, and other clinical areas. She has worked as part of the hospital’s certification team and has strong background in quality assurance.

Over the years, she has been heavily involved in development of the NZ standard CTR and Indemnity Agreements, worked as part of many national and international groups in clinical research and truly considers herself as jack of all trades when it comes to clinical trials.