CSUR Research and Consultancy
Study Manager
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Study Manager
Study Manager
Centre for Substance Use Research (CSUR) – Glasgow
Are you a highly organised and motivated Study Manager looking to make a meaningful impact in tobacco regulatory science?
CSUR is a contract research organisation conducting world-leading regulatory science research to evaluate the public health impact of tobacco and nicotine products. We collaborate with international clients to design and deliver high-quality research for regulatory submissions globally.
We are seeking a Study Manager to join our Glasgow-based team, with responsibility for managing Actual Use Studies (AUS), Randomized Controlled Trials (RCTs), and Longitudinal Cohort Studies. This role involves:
- Collaborating with scientific teams, research partners, and clients.
- Ensuring studies meet highest scientific and operational standards across a dynamic portfolio of projects.
- Thriving in a fast-paced environment with multiple concurrent studies.
Key Responsibilities
- Coordinate or manage research studies or clinical research projects.
- Oversee multiple studies simultaneously, meeting deadlines under time and budget constraints.
- Prepare, maintain, and track study documentation and report progress.
- Communicate effectively with internal teams, research partners, and clients.
- Utilise Microsoft Excel for data organisation, monitoring, and analysis.
- Manage datasets in SPSS (or equivalent) for statistical analysis and quality checks.
- Interpret study data and grasp fundamental statistical concepts.
- Develop scientific reports, presentations, and study documentation.
- Anticipate and resolve operational issues using practical solutions.
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Core Requirements
- Proven project management experience in research or clinical settings.
- Ability to organise workflows for multiple studies, balancing deadlines efficiently.
- Strong attention to detail with high accuracy standards.
- Proficiency in Microsoft Excel and statistical software.
- Project reporting skills, including preparing research documentation.
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Desirable Talent
- Experience in Actual Use Studies, Randomised Controlled Trials, or cohort-based research.
- Background in CROs, academic, or clinical research.
- Expertise in participant recruitment/retention or vendor/site management.
- Familiarity with Good Clinical Practice (GCP) or Standard Operating Procedures (SOPs).
- Published scientific research in peer-reviewed journals.
- Knowledge of tobacco regulatory science, harm reduction, or behavioural research.
About the Role
Initially fixed-term for five years. The position offers:
- Competitive salary with a performance-based bonus.
- Royal London pension (generous contribution).
- Access to private health and life insurance.
- A digital-friendly office in Glasgow’s West End (Fridays optional). Hybrid arrangements are possible on request.
How to Apply
If this excites you, send your CV and covering letter to: Ms. Suman Joshi joshi@csures.com
Interviews run on a rolling basis until filled.
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