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- Tasks: Lead multicentre clinical research studies and manage the BRIDGE study focused on respiratory diseases.
- Company: Join a dynamic research team at Ninewells Hospital, one of Europe's largest teaching hospitals.
- Benefits: Gain experience in cutting-edge research and collaborate with top scientists across Europe.
- Why this job: Make a real impact in personalized medicine while working in a supportive, innovative environment.
- Qualifications: MSc in nursing, biomedical, life sciences, or relevant discipline; 3 years' clinical research experience required.
- Other info: Travel across the UK and Europe is expected; strong teamwork and communication skills are essential.
The predicted salary is between 43200 - 72000 £ per year.
We are recruiting for a Research Project Manager within our Group to lead a portfolio of multicentre clinical research studies as part of a dynamic research team.
The role holder’s primary focus will be the BRIDGE study, a multicentre pan-European study aiming to recruit 1000 patients with respiratory disease into an observational study in which patients will donate multiple biological samples for next generation sequencing, "omics" analysis and detailed phenotyping leading to the development of personalised medicine.
The role holder will also provide support across other studies within the respiratory team. Working closely with the Chief Investigator (CI), local and site research teams as well as scientists and data management team to ensure the implementation of all aspects of the study, including research governance, maintaining ethical and regulatory approval, communication with and training of staff at collaborating sites, promoting the study to research networks and patient groups, maintaining trial documentation and reporting.
As the portfolio consists of multi-centre studies travel to sites across the UK and Europe will be expected.
Based in Ninewells Hospital, one of Europe’s largest teaching hospitals, the School of Medicine provides outstanding medical education and training supported by world class research facilities.
Your priorities will include:
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Working with the CI, the study team, the Research Nurses, third party stake holders, including patient groups and external laboratories. The post holder will be responsible for co-ordinating the clinical research portfolio on behalf of the CI and will be the primary contact for study collaborators, clinicians, research nurses and study participants. The studies must be run to the expected UK regulatory standards and in line with TASC policies and procedures.
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Work with the CI and sites to introduce and maintain common working practices and SOPs and to identify training requirements of local and participating site trial personnel. This includes protocol development, management of ethical and regulatory approval and the establishment of governance issues.
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Ensure accurate collection and recording of data and maintenance of study documentation across local and national study teams. Create and populate local Trial Master Files and issue Site Files to participating centres. Collate site agreements and evidence of local approvals.
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Ensure the timely recruitment of study participants. Monitor the study progress to ensure compliance with and adherence to the project plan and to identify and rectify problems as they arise.
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Work with investigators, ethics committee(s), regulatory authorities, and local governance office to manage any changes to study documentation.
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A minimum of an MSc in nursing, biomedical, life sciences or other relevant discipline
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At least 3 years’ experience working in clinical research.
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Good knowledge of current scientific, regulatory and ethical frameworks defining trial management activity
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Practical knowledge of academic trial management
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The ability to work effectively within a multi-disciplinary research team
For further information about this position please contact Professor James Chalmers- j.chalmers@dundee.ac.uk To find out more about the Chalmers group please visit www.bronchiectasis.eu and https://www.dundee.ac.uk/medicine/staff/profile/james-chalmers.php.
Research Project Manager - UOD1846 employer: University of Dundee
Contact Detail:
University of Dundee Recruiting Team
j.chalmers@dundee.ac.uk
StudySmarter Expert Advice 🤫
We think this is how you could land Research Project Manager - UOD1846
✨Tip Number 1
Familiarize yourself with the BRIDGE study and its objectives. Understanding the specifics of this multicentre pan-European study will help you demonstrate your knowledge and enthusiasm during interviews.
✨Tip Number 2
Network with professionals in the clinical research field, especially those involved in respiratory studies. Engaging with current or former team members can provide insights into the role and may even lead to a referral.
✨Tip Number 3
Highlight your experience in managing multi-centre studies and your familiarity with UK regulatory standards. Be prepared to discuss specific examples of how you've ensured compliance and maintained ethical standards in past projects.
✨Tip Number 4
Prepare to discuss your approach to training and supporting site personnel. The role requires effective communication and collaboration, so showcasing your ability to foster teamwork will be crucial.
We think you need these skills to ace Research Project Manager - UOD1846
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Research Project Manager position. Understand the key responsibilities, such as leading multicentre clinical research studies and working closely with various stakeholders.
Highlight Relevant Experience: In your application, emphasize your experience in clinical research, particularly any roles that involved managing studies or working with regulatory frameworks. Mention specific projects or studies you've been involved in that relate to the BRIDGE study.
Showcase Teamwork Skills: Since the role requires working within a multi-disciplinary research team, provide examples of how you've successfully collaborated with others in previous positions. Highlight your ability to communicate effectively with diverse groups.
Tailor Your CV and Cover Letter: Customize your CV and cover letter to reflect the skills and experiences that align with the job requirements. Use keywords from the job description to demonstrate that you are a good fit for the position.
How to prepare for a job interview at University of Dundee
✨Understand the BRIDGE Study
Make sure you have a solid grasp of the BRIDGE study's objectives and methodologies. Familiarize yourself with the specifics of multicentre clinical research, especially in respiratory diseases, as this will demonstrate your commitment and understanding of the role.
✨Showcase Your Experience
Prepare to discuss your previous experience in clinical research, particularly any roles that involved managing studies or working with diverse teams. Highlight specific examples where you successfully navigated regulatory frameworks or ethical considerations.
✨Emphasize Team Collaboration
Since the role requires working closely with various stakeholders, be ready to share examples of how you've effectively collaborated with multidisciplinary teams. Discuss your communication skills and how you’ve trained or supported team members in past projects.
✨Prepare for Ethical and Regulatory Questions
Anticipate questions related to ethical and regulatory standards in clinical trials. Brush up on current guidelines and be prepared to discuss how you would ensure compliance and manage documentation throughout the study lifecycle.
