Study Manager

Are you a highly organised and motivated Study Manager looking to make a meaningful impact in tobacco regulatory science? The Centre for Substance Use Research (CSUR) is a contract research organisation conducting world-leading regulatory science research to evaluate the public health impact of tobacco and nicotine products. We work with international clients to design and deliver high-quality research that supports regulatory submissions around the world.

We are seeking a Study Manager to join our team in Glasgow. This is an exciting opportunity to manage a diverse portfolio of research studies, including Actual Use Studies (AUS), Randomized Controlled Trials (RCTs), and Longitudinal Cohort Studies. You will work closely with our scientific team, research partners, and international clients to ensure studies are delivered to the highest scientific and operational standards. Our work is conducted within a dynamic, fast-paced environment where multiple studies are often running simultaneously.

The successful candidate will thrive under pressure, enjoy solving complex operational challenges, and take pride in delivering high-quality research on time and to budget. To be successful in this role, you should have experience in:

• Coordinating or managing research studies or clinical research projects
• Managing multiple projects simultaneously while meeting competing deadlines
• Preparing and maintaining study documentation and tracking study progress
• Communicating effectively with internal teams, external research partners, and clients
• Using Microsoft Excel to organise, monitor, and analyse study data
• Using SPSS (or equivalent statistical software) for data management and basic statistical analyses
• Interpreting study data and understanding fundamental statistical concepts
• Preparing scientific reports, presentations, or other research documentation
• Identifying operational issues and implementing practical solutions to keep studies on track
• Working with exceptional attention to detail while maintaining high levels of accuracy

The ideal candidate will also demonstrate:

• Excellent organisational and time management skills
• Strong problem-solving ability and sound judgement
• Outstanding written and verbal communication skills
• Confidence working independently while collaborating effectively within a multidisciplinary team
• The ability to prioritise workload in a fast-moving, time-critical environment
• A proactive approach with a willingness to take ownership of projects

Experience working within regulated research environments or following Standard Operating Procedures (SOPs) is preferred. We'd particularly like to hear from you if you have experience with:

• Actual Use Studies, Randomised Controlled Trials, or longitudinal observational studies
• Contract research organisations (CROs), academic research, or clinical research
• Participant recruitment and retention strategies
• Managing external vendors or research sites
• Preparing study protocols, study reports, or research proposals
• Publishing scientific research in peer-reviewed journals
• Tobacco regulatory science, tobacco harm reduction, nicotine products, or behavioural research
• Working under Good Clinical Practice (GCP) or other quality management systems

This role is initially available for five years. We offer a competitive salary together with an attractive benefits package, including:

• Performance-based bonus scheme
• Generous Royal London pension
• Private health insurance
• Life insurance

Our office is based in a beautiful townhouse conversion in Glasgow's West End. We work primarily from the office, with the opportunity to work from home on Fridays. If you are interested in joining our team, please send your CV and a covering letter to Ms. Suman Joshi at joshi@csures.com. Interviews will be held on a rolling basis until the position is filled.