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- Tasks: Manage clinical trials, ensuring data integrity and patient safety.
- Company: Join a leading UK CRO with a supportive team culture.
- Benefits: Competitive salary, healthcare plan, and generous annual leave.
- Other info: Enjoy a hybrid work model with excellent growth opportunities.
- Why this job: Make a real impact in drug development while advancing your career.
- Qualifications: 2 years CRA experience and a science degree required.
The predicted salary is between 36000 - 60000 £ per year.
An exciting opportunity working with a UK leading CRO. CRO Solutions, an IQVIA business, is recruiting for an experienced CRA (CRA II) to join an existing team of established CRAs, working on a range of clinical trials. The position will be a hybrid role of office based (in our premises in Salford, Manchester) and work from home when not monitoring at study sites. Clinical trial experience is essential for this permanent role, which would suit a well-motivated, enthusiastic and organised person who is able to work independently, as well as within an established team.
Responsibilities:
- Site selection, training and management
- Providing the highest quality collection and review of data and source documentation/case report forms
- Ensuring data integrity, patient safety and regulatory compliance
- Accountable for protocol compliance
- Resolving data queries
- Conducting interim analyses as required
Qualifications:
Ideal candidates will have 2 years of CRA experience, be educated to a Bachelors science degree or equivalent and have an in-depth knowledge and understanding of drug development/research including ICH GCP. As well as good communication and organisational skills, you will also have excellent IT skills using MS Office.
Benefits:
- Competitive salary, dependent on experience
- Immediate start
- Career progression opportunities
- Continuous professional development
- 29 days annual leave plus Bank Holidays, rising to 33 days after 5 years service
- Attractive company pension scheme
- Healthcare plan
- Free on-site parking
Clinical Research Associate II in Salford employer: Anne-Dorthe Wilms
Contact Detail:
Anne-Dorthe Wilms Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate II in Salford
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Familiarise yourself with their recent trials and be ready to discuss how your experience aligns with their needs. This shows you're genuinely interested and well-prepared!
✨Tip Number 3
Practice your responses to common interview questions, especially those related to data integrity and patient safety. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your achievements.
✨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 take the initiative to connect directly with us.
We think you need these skills to ace Clinical Research Associate II in Salford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate II role. Highlight your relevant experience, especially in clinical trials, and showcase your skills in data management and compliance. We want to see how you fit into our team!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your enthusiasm for the role and explain why you're the perfect fit. Mention specific experiences that relate to the responsibilities listed in the job description.
Showcase Your Skills: Don’t forget to highlight your IT skills, especially with MS Office, as well as your communication and organisational abilities. We’re looking for someone who can work independently and as part of a team, so make sure to reflect that in your application.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates regarding your application status!
How to prepare for a job interview at Anne-Dorthe Wilms
✨Know Your Clinical Trials
Make sure you brush up on your knowledge of clinical trials and the specific studies the company is involved in. Being able to discuss recent developments or challenges in the field will show your enthusiasm and expertise.
✨Showcase Your Organisational Skills
As a CRA II, you'll need to demonstrate strong organisational skills. Prepare examples from your past experience where you've successfully managed multiple tasks or projects, especially in a clinical setting. This will highlight your ability to work independently and as part of a team.
✨Prepare for Data Integrity Questions
Expect questions about data integrity and regulatory compliance. Familiarise yourself with ICH GCP guidelines and be ready to discuss how you've ensured compliance in previous roles. This will show that you understand the importance of these aspects in clinical research.
✨Practice Your Communication Skills
Good communication is key in this role. Practice articulating your thoughts clearly and concisely. You might even want to do a mock interview with a friend to get comfortable discussing your experiences and answering questions confidently.