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- Tasks: Build strategic relationships with clinical research sites to optimise clinical trials.
- Company: Join a leading organisation in clinical research with a focus on innovation.
- Benefits: Career advancement, skill development, and a dynamic work environment.
- Why this job: Make a real impact in clinical research while growing your professional skills.
- Qualifications: University degree or equivalent experience; understanding of clinical practices is a plus.
- Other info: Opportunity to work on multiple projects and enhance your career in a supportive setting.
The predicted salary is between 36000 - 60000 £ per year.
We are in search of an experienced professional dedicated to developing strategic relationships with clinical research sites, with the aim of optimizing and advancing the progress of clinical trials. This is the main responsibility of a site ID specialist.
Responsibilities:
- Communicate and build relationships with clinical sites to identify potential centres for clinical trials.
- Maintain and refine internal site databases in cooperation with Study Startup, Clinical Operations and Process Improvement.
- Conduct site identification activities, including discussion of clinical trial protocols and collection of site identification questionnaires during the startup phase of the clinical trials.
- Define the main study objectives and the optimal site profile.
- Create an initial list of potential sites.
- Communicate with project teams on project/regional level to fine-tune strategy and methodology of initial and follow-up site contacts depending on indication, regional specifics, and technologies in use.
- In cooperation with the project team, maintain a study site identification tracker for further site evaluation and selection activities.
- Liaise with project teams to evaluate status and progress of site identification, to identify and highlight any potential risks or issues to timelines or objectives.
- In cooperation with Legal, perform due diligence check of regulatory and legal limitations applicable to the recommended investigators or clinical sites.
- Support the project team throughout study startup and further on, whenever additional rounds of site identification are necessary, and/or additional information on the site/investigator is needed.
Qualifications:
- University/college degree (MD/PharmD degree), or an equivalent combination of education, training and experience.
- On-site monitoring experience is a plus.
- Understanding of Good Clinical Practice, local laws and applicable regulations in the region.
- Demonstrated ability to work in a dynamic environment, under compressed deadlines across several projects, each with unique requirements.
Advance your career in clinical research and develop new skillsets whilst growing with the organization.
Site Identification Specialist in Oxford employer: PSI CRO
Contact Detail:
PSI CRO Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Site Identification Specialist in Oxford
✨Tip Number 1
Networking is key! Reach out to professionals in the clinical research field on LinkedIn or at industry events. Building relationships can open doors to opportunities that aren’t even advertised.
✨Tip Number 2
Don’t just apply and wait! Follow up on your applications with a friendly email or message. It shows your enthusiasm and keeps you on their radar, which can make a difference.
✨Tip Number 3
Prepare for interviews by researching the company and understanding their projects. Tailor your responses to highlight how your skills align with their needs, especially in site identification and relationship building.
✨Tip Number 4
Apply through our website for the best chance! We love seeing candidates who take the initiative to engage directly with us. Plus, it helps us keep track of your application more easily.
We think you need these skills to ace Site Identification Specialist in Oxford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Site Identification Specialist role. Highlight your experience in building relationships with clinical sites and any relevant qualifications that match the job description.
Craft a Compelling Cover Letter: Your cover letter should tell us why you're the perfect fit for this role. Share specific examples of how you've successfully identified and engaged with clinical research sites in the past.
Showcase Your Skills: Don’t forget to mention your understanding of Good Clinical Practice and any on-site monitoring experience. We want to see how your skills align with our needs!
Apply Through Our Website: For the best chance of success, apply directly through our website. This way, we can easily track your application and get back to you quicker!
How to prepare for a job interview at PSI CRO
✨Know Your Stuff
Make sure you brush up on clinical trial protocols and Good Clinical Practice. Being able to discuss these topics confidently will show that you’re not just familiar with the basics, but that you understand the nuances of site identification.
✨Build Your Network
Before the interview, think about your past experiences in building relationships with clinical sites. Be ready to share specific examples of how you’ve successfully identified potential centres and maintained those connections.
✨Show Your Organisational Skills
Since this role involves maintaining databases and trackers, be prepared to discuss how you manage multiple projects and deadlines. Share any tools or methods you use to stay organised and ensure nothing slips through the cracks.
✨Ask Smart Questions
Prepare thoughtful questions about the company’s current projects and challenges in site identification. This shows your genuine interest in the role and helps you understand how you can contribute to their success.
