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- Tasks: Manage early phase clinical studies and ensure smooth execution with a cross-functional team.
- Company: Hobson Prior connects talented individuals with top life sciences opportunities worldwide.
- Benefits: Gain hands-on experience in a dynamic environment with potential for growth and innovation.
- Why this job: Join a collaborative team focused on patient-centric solutions and make a real impact in healthcare.
- Qualifications: University degree or equivalent experience in life sciences; prior study management experience preferred.
- Other info: This role requires the right to work in the specified location.
The predicted salary is between 36000 - 60000 £ per year.
As a contract Study Manager, you will be assigned to pRED early phase clinical studies, and as part of a cross-functional study team, you will be responsible for delivering study management and clinical operations activities under the direction and leadership of a pRED Study Management Team Leader.
Please note that to be considered for this role you must have the right to work in this location.
What you will be doing:
During your assignment you will participate as a member of the Study Management Team contributing to the delivery and execution of early phase study protocols.
You will:
- DELIVER STUDY EXECUTION by providing operational expertise into protocol design and feasibility, country selection, patient centricity and data delivery plans in partnership with cross-functional stakeholders. Ensure study quality and integrity by developing and maintaining study systems and documentation (including informed consent forms, communication plan, Trial Monitoring Plan, Trial Master File etc.).
- PROVIDE COUNTRY OVERSIGHT, for insourced studies, by supporting or managing feasibility assessments to ensure countries and sites are selected for participation in studies. Provide guidance to country operational representatives during studies to ensure countries start on time and deliver on their recruitment commitments.
- MANAGE VENDOR PERFORMANCE by providing direction and actively managing relationships. Ensure vendors and third-party suppliers deliver against contracted work and performance expectations and adhere to all appropriate standards (including ICH/GCP, SOPs and other regulations).
- PLAN DEMAND AND SUPPLY by overseeing the forecasting and maintenance of supplies (including IMP) needed to ensure sites have the necessary resources to run clinical studies.
- MANAGE RISK AND COMPLIANCE by assisting the study team in the identification, management and mitigation of study-related risks and issues in your areas of responsibility (including oversight of the risk, action and decision logs).
- DRIVE OPERATIONAL EXCELLENCE by providing operational expertise across a range of operations-related activities that drive improvement and consistency in the execution of clinical studies
Who are you:
You are talented and passionate. You are inspired by our mission and would t in well with our collaborative, patient-centric and entrepreneurial spirit.
- Having a growth mindset and are excited about learning through experience
- Feel comfortable thinking on your feet and thrive in fast-paced, ambiguous and highly collaborative environments
- Hold a university degree or equivalent years of experience (preferred focus in life sciences)
- Have demonstrated strong and consistent performance as a Study Manager (or equivalent) in pharmaceutical and/or healthcare industry and drug development experience (therapeutic area experience a plus)
- A self-starter who has a passion for achieving successful outcomes and delivering excellence
- Want to make a difference and excitement in innovating practices and challenging conventions.
- Possess strong working knowledge of drug development process and respective regulations, including ICH and GCP guidelines
For more information, please contact Grant Van Schalkwyk.
If you are interested in applying to this exciting opportunity, then please click \’Apply\’ or to speak to one of our specialists visit the \’Contact Us\’ page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you\’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.hobsonprior.com/privacy-policy.
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Study Manager employer: Hobson Prior
Contact Detail:
Hobson Prior 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 compliance effectively. Highlighting your problem-solving skills in real-world scenarios can set you apart from other candidates.
✨Tip Number 4
Showcase your passion for patient-centricity by discussing how you've previously prioritised patient needs in study designs. This aligns with our mission and demonstrates that you share our values, making you a more attractive candidate.
We think you need these skills to ace Study Manager
Some tips for your application 🫡
Understand the Role: Take time to thoroughly read the job description for the Study Manager position. Understand the key responsibilities and required skills, as this will help you tailor your application to highlight relevant experiences.
Tailor Your CV: Customise your CV to reflect your experience in study management and clinical operations. Emphasise your achievements in previous roles, particularly those that align with the responsibilities outlined in the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the role and the company. Highlight your relevant experience, your understanding of the drug development process, and how you can contribute to the team’s success.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial for a Study Manager.
How to prepare for a job interview at Hobson Prior
✨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 but also helps you gauge if the company culture aligns with your values, especially regarding patient-centric practices.
