Meet the TEAM

Meet the Team: Rebecca (Becs) Davies
Senior Global Drug Safety Manager.

Rebecca Davies
Rebecca Davies
Senior Global Drug Safety Manager

Rebecca has over 20 years strategic and operational experience in global Pharmacovigilance in both large pharma and small to medium sized pharma organizations.

Rebecca has acted in the capacity of UK QPPV and her expertise spans across the product lifecycle from multiple GxP perspectives having worked in GVP, GMP, GCP and GDP.

She has supported both GMP and GVP Health Authority inspections including EMA, FDA, MHRA, ANSM, Health Canada, HPRA,TGA, BSI and AIFA.

Tell us about a day in the life of a Senior Global Drug Safety Manager.

No two days are ever alike! As the Senior Global Drug Safety Manager overseeing the Safety Data Management, Clinical Safety and Medical Writing teams I can be asked to partake in many activities, from answering queries, working directly with clients or working with Business Development.  My favorite activities are working with my teams on process improvements to help us work smarter and deliver efficiencies.

I have an inquisitive mind so I love the opportunity to challenge our processes and really encourage my teams and colleagues to bring ideas to the table to help us stay at the front of our field.

What do you like best about collaborating with clients?

For me it is meeting different teams, hearing about their passion for their products and their patients, and working out how to work as part of their organization to achieve their goals.

As someone who has come from a R&D company, who went through the early stage development to commercialization struggles, I really get their passion, and I feel privileged on each contract awarded and to become part of their story.

Nothing makes me happier than helping to get products to patients and changing their lives.

I recently attended the VEEVA summit in Boston and met so many great passionate individuals, many of whom I hope that we will collaborate with in the future because they are doing incredible work for patients.

What is a current trend you are seeing in the industry and how does it impact our clients and patients?

Incredibly fast paced innovation! Fields like oncology, rare disease, real life changing medicines, together with the ATMPs, are changing the game for the industry and most importantly patients. Arriello are working on numerous Early Access Programs / Managed Access Programs for our clients, which is so exciting because of the potential to change lives and give hope.

Technology is also playing a bigger part than ever so solutions are becoming increasingly tailored to individual patients which is both inspirational and challenging as we adapt to be able to deal with the demands of this ever-changing world!

What is unique about working for Arriello?

Working with a team of likeminded driven people who are all so committed to one goal. We are a growing organization for sure, but we retain a real sense of family within our teams – collaborating constantly with one another to achieve our goals, both client and personal.

As a real mixed team – from across many geographic locations, backgrounds, and industries – conversations to discuss approaches and solutions can be very entertaining and outcomes can be quite unexpected because of the broad perspective that we offer, but I believe that is what makes us so unique and fun to work with!