Sophia, Data Sciences Manager
I meet with different colleagues from across my organisation (eg physicians, computer programmers, statisticians, clinicians, regulatory affairs, health outcomes, contracts) to discuss various data quality aspects of my assigned clinical trials. The objective being to ensure that by the end of my trial the data collected accurately reflects all events and tests that occurred throughout the duration of that trial and to address any anomalies (particularly those anomalies that meant the patient did not adhere to the study protocol). In this role it’s important that anomalies are addressed in a timely manner therefore placing subject safety and well-being first.
Some aspects of my studies are outsourced. This is currently a popular model in this industry as it allows staff in our company to focus on the overall project deliverables. So as a result I am in frequent contact with other third party companies (vendors) across the globe who process some aspects of our data on our behalf.
From time to time I’m required to deliver training on the more challenging parts of the study where it relates to the ensuring the quality of the data to be collected, eg diary data, logistics to an extension study.
Training along with meetings when not face to face often take place via telephone conferencing (TCs) or video conferencing (VTC). A meeting agenda is usually sent out in advance which helps to keep the meeting focused as well as to allow the meeting participants to prepare their input.
This varies from time to time but currently I work as part of a core team of six and wider team of approximately 10. In addition to this are our outsourcing partners sometimes known as ‘Strategic Alliance Partners’.
Two years in this role.
I have an honours degree (BSc) in Pharmacology and a Post Graduate Diploma in Management.
I loved watching the medical dramas on TV as a youngster and wanted to find my own niche where I could help others in a related way.
I have worked in other areas such as medical publishing, clinical pathology, scientific event management and more recently in clinical trials. I’m fortunate that all aspects of my prior experience have always proved to be extremely valuable and continue to contribute to my career path often allowing me to have a bigger or more holistic picture of projects to which I’m assigned.
I believe work experience can significantly augment any qualifications you may have. This often provides a substantial leverage plus let’s you get a feel for if this is something you really want to do!
Temporary work is a great way to get a wide and varied exposure to the industry. Strongly consider any unpaid opportunities. Maybe not so lucrative in immediate monetary terms, but could pay pidends in the future.
Everyone is very friendly and stops for a chat especially at the Starbucks we have in our building!
Knowing that the creative, innovative ideas that I have contributed to in my different roles have always been very appreciated particularly where leading to improvements in the way things are done.
My company has a number of sites globally and many different departments within research and development, manufacturing, through to consumer health and as such continues to provide opportunities for career development by way of mentoring secondments or indeed by changing role within the company.
Get advice/mentoring on developing a great, eye catching CV that really details the skills that you can offer. Try contacting STEMNET, your careers advisor or even the HR department of a pharmaceutical company that interests you.