At a Glance
- Tasks: Monitor clinical sites and ensure compliance with study protocols in Oncology.
- Company: Join a leading organisation making a difference in cancer research.
- Benefits: Full-time role with opportunities for travel and professional growth.
- Other info: Dynamic role with continuous learning and development opportunities.
- Why this job: Make a real impact in healthcare while advancing your career.
- Qualifications: Experience in Oncology monitoring and knowledge of GCP guidelines required.
The predicted salary is between 35000 - 45000 £ per year.
The Clinical Research Associate will support Oncology studies and cover sites across the UK. Apply today and forge a career with greater purpose, make an impact and never stop learning!
Responsibilities
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
Requirements
- Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
- In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Life science degree educated or equivalent industry experience.
- Flexibility to travel to sites as required.
Clinical Research Associate in Manchester employer: LinkedIn
Join a leading organisation in the clinical research field, where you will have the opportunity to make a significant impact on Oncology studies across the UK. Our supportive work culture fosters continuous learning and professional growth, ensuring that you are equipped with the skills and knowledge to excel in your role. With a commitment to employee development and a focus on collaboration, we offer a rewarding environment that values your contributions and encourages innovation.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate in Manchester
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field, especially those working in oncology. Attend industry events or webinars to make connections and learn about potential job openings.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Be ready to discuss how your experience aligns with the responsibilities of a Clinical Research Associate.
✨Tip Number 3
Showcase your flexibility and willingness to travel during interviews. Highlight any previous experiences where you successfully managed site visits or adapted to changing project needs.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Clinical Research Associate in Manchester
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate role. Highlight your experience in Oncology studies and any relevant skills that match the job description. We want to see how you can make an impact!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your background aligns with our mission at StudySmarter. Keep it engaging and personal!
Showcase Your GCP Knowledge:Since Good Clinical Practice is key for this role, make sure to mention your understanding of GCP and ICH guidelines. We’re looking for someone who knows their stuff and can ensure quality in our studies.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and keep track of all the amazing candidates. Plus, it shows you’re keen on joining the StudySmarter team!
How to prepare for a job interview at LinkedIn
✨Know Your Oncology Stuff
Make sure you brush up on your knowledge of oncology studies and the specific challenges they present. Familiarise yourself with recent advancements in the field, as well as any relevant GCP and ICH guidelines. This will show that you're not just interested in the role but are also passionate about making a real impact.
✨Demonstrate Your Monitoring Skills
Be ready to discuss your experience with site monitoring visits. Prepare examples of how you've handled selection, initiation, and close-out visits in the past. Highlight any specific challenges you faced and how you overcame them, as this will showcase your problem-solving abilities and attention to detail.
✨Communication is Key
Since you'll be working closely with sites, it's crucial to demonstrate your communication skills. Think of examples where you've successfully established lines of communication with study sites or managed project expectations. This will help the interviewers see that you can foster strong relationships and keep everyone on the same page.
✨Show Your Organisational Skills
As a Clinical Research Associate, you'll need to manage multiple tasks simultaneously. Be prepared to discuss how you track regulatory submissions, recruitment, and data queries. Share specific tools or methods you use to stay organised, as this will reassure the interviewers that you can handle the demands of the role effectively.
