At a Glance
- Tasks: Monitor clinical sites and ensure compliance with study protocols in oncology research.
- Company: Join a leading organisation dedicated to advancing cancer research.
- Benefits: Full-time role with opportunities for travel, learning, and career growth.
- Other info: Dynamic role with a focus on collaboration and continuous learning.
- Why this job: Make a real impact in the fight against cancer while developing your skills.
- Qualifications: Experience in oncology monitoring and knowledge of GCP and ICH guidelines.
The predicted salary is between 30000 - 40000 € 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 Chesterfield employer: LinkedIn
Join a forward-thinking organisation in Chesterfield, where as a Clinical Research Associate, you will be part of a dynamic team dedicated to advancing Oncology studies. We pride ourselves on fostering a collaborative work culture that prioritises employee growth and continuous learning, offering comprehensive training and development opportunities. With a commitment to making a meaningful impact in the healthcare sector, we provide a supportive environment that values innovation and excellence.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate in Chesterfield
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Clinical Research Associate role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of Good Clinical Practice (GCP) and Oncology studies. We recommend practising common interview questions with a friend or mentor to boost your confidence and show off your expertise.
✨Tip Number 3
Don’t just apply and wait! Follow up on your applications through our website. A quick email or message can show your enthusiasm and keep you on the radar of hiring managers.
✨Tip Number 4
Showcase your flexibility and willingness to travel in your conversations. As a Clinical Research Associate, being adaptable is key, so let’s highlight that in your discussions with potential employers!
We think you need these skills to ace Clinical Research Associate in Chesterfield
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, be sure to mention your understanding of GCP and ICH guidelines. We’re looking for someone who knows their stuff and can ensure quality and integrity in study practices.
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 our 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 a candidate, but someone who is genuinely interested and informed.
✨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.
✨Communication is Key
Since the role involves liaising with various sites, practice articulating how you establish and maintain communication with stakeholders. Think of examples where you successfully managed expectations or resolved issues through effective communication. This will demonstrate your interpersonal skills and ability to work collaboratively.
✨Show Your Organisational Skills
The role requires managing multiple studies and tracking various documents. Be prepared to discuss your organisational strategies and tools you use to keep everything in order. Mention any experience you have with maintaining Trial Master Files (TMF) and Investigator's Site Files (ISF), as this will highlight your attention to detail.
