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- Tasks: Manage early phase clinical studies and ensure operational excellence.
- Company: Hobson Prior connects talented individuals with top life sciences roles globally.
- Benefits: Gain hands-on experience in a dynamic, collaborative environment with growth opportunities.
- Why this job: Join a mission-driven team focused on patient-centric innovation and impactful drug development.
- Qualifications: University degree or equivalent experience in life sciences; strong performance as a Study Manager preferred.
- Other info: Remote work options may be available; must have the right to work in the location.
The predicted salary is between 36000 - 60000 £ per year.
Contract Study Manager – 6-Month Assignment (Hybrid, Welwyn, UK)We are seeking an experienced Contract Study Manager to support early-phase clinical development projects within a leading pharmaceutical environment. This role is ideal for professionals with proven experience in clinical study management, vendor oversight, and cross-functional study operations.Key DetailsContract Length: 6 months (starting 22 September 2025)Location: Hybrid – 2 days per week on site in Welwyn, UK (AL6)IR35 Status: Inside IR35 (umbrella)ResponsibilitiesLead and oversee clinical study execution across global cross-functional teams.Manage vendors, CROs, and third-party providers to ensure compliance, timelines, and quality.Ensure adherence to ICH-GCP, regulatory requirements, and drug development processes.Drive operational excellence in study planning, risk management, and documentation.Collaborate with internal stakeholders on patient-centric and innovative trial approaches.Essential RequirementsPrior experience as a Study Manager / Clinical Study Manager / Clinical Operations Manager / Trial Manager in pharma, biotech, or CRO.Strong knowledge of ICH-GCP, clinical research regulations, and study governance.Demonstrated ability to manage vendors and global study operations.Degree in Life Sciences (or equivalent experience).Preferred ExperienceEarly-phase (Phase I–II) study management.Advanced degree in Life Sciences.Familiarity with innovative trial design and patient-focused studies.Candidate Profile We are looking for hands-on Study Managers who thrive in fast-paced environments, bring operational expertise, and collaborate effectively across global teams. Candidates without direct study management experience, purely academic backgrounds, or overly senior strategic profiles will not be considered.
Study Manager employer: LinkedIn
Contact Detail:
LinkedIn Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Study Manager
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in clinical study management, particularly ICH and GCP guidelines. This knowledge will not only help you during interviews but also demonstrate your commitment to operational excellence.
✨Tip Number 2
Network with professionals in the pharmaceutical and healthcare industries. Attend relevant conferences or webinars to connect with others in the field, as personal recommendations can significantly boost your chances of landing the job.
✨Tip Number 3
Prepare to discuss specific examples from your past experiences that showcase your ability to manage risks and ensure compliance in clinical studies. Highlighting your problem-solving skills will set you apart from other candidates.
✨Tip Number 4
Showcase your passion for patient-centricity by discussing how you've previously engaged with patients or stakeholders to improve study outcomes. This aligns well with our mission and will resonate with the hiring team.
We think you need these skills to ace Study Manager
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Study Manager. Familiarise yourself with the key tasks mentioned in the job description, such as study execution, country oversight, and vendor performance management.
Tailor Your CV: Customise your CV to highlight relevant experience in clinical studies and drug development. Emphasise your operational expertise, risk management skills, and any specific achievements that align with the requirements of the role.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the role and the company. Mention your growth mindset, collaborative spirit, and how your background in life sciences makes you a suitable candidate for this position.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for any spelling or grammatical errors, and ensure that all information is clear and concise. A polished application reflects your attention to detail.
How to prepare for a job interview at LinkedIn
✨Understand the Role
Make sure you thoroughly understand the responsibilities of a Study Manager. Familiarise yourself with early phase clinical studies, protocol design, and the importance of patient centricity. This will help you answer questions confidently and demonstrate your knowledge.
✨Showcase Your Experience
Prepare to discuss your previous experience in study management or related roles. Highlight specific examples where you've successfully managed studies, dealt with vendors, or ensured compliance with regulations like ICH and GCP. This will show that you have the practical skills needed for the job.
✨Demonstrate Team Collaboration
Since this role involves working within a cross-functional team, be ready to share examples of how you've collaborated with others in the past. Emphasise your ability to communicate effectively and work towards common goals, as this is crucial in a fast-paced environment.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's approach to study management and their expectations for the role. This not only shows your interest in the position but also helps you gauge if the company culture aligns with your values and work style.
