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- Tasks: Manage clinical trials, ensuring data integrity and patient safety while working with a dynamic team.
- Company: CRO Solutions, part of IQVIA, known for its supportive and innovative culture.
- Benefits: Competitive salary, generous leave, healthcare plan, and career progression opportunities.
- Why this job: Join a vital role in drug development and make a real difference in patient care.
- Qualifications: 1 year of CRA experience and a Bachelor’s science degree or equivalent required.
- Other info: Hybrid work model with potential for permanent position after maternity cover.
The predicted salary is between 36000 - 60000 £ per year.
CRO Solutions®, an IQVIA business, is recruiting for a 12-month maternity cover CRA I position 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 role, which would suit a well-motivated, enthusiastic and organised person who is able to work independently, as well as within an established team.
The RoleThe successful candidate will be responsible for:
- 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
Ideal candidates will have at least 1 year of CRA experience, be educated to a Bachelor’s 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.
CRO-Solutions will offer you:- Competitive salary, dependent on experience
- Immediate start
- Career progression opportunities
- Potential to make role permanent after completion of cover
- 29 days annual leave plus Bank Holidays, (rising to 33 days after 5 years’ service)
- Attractive company pension scheme
- Generous annual bonus
- Healthcare plan
- Free on-site parking
Clinical Trials Administrator - (Maternity Cover) in Salford employer: CRO-Solutions®, an IQVIA business
Contact Detail:
CRO-Solutions®, an IQVIA business Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trials Administrator - (Maternity Cover) in Salford
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical trials 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 understanding their projects. Be ready to discuss how your experience aligns with their needs, especially in site selection and data integrity. Show them you’re not just another candidate, but the right fit!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a quick thank-you email to express your appreciation and reiterate your interest in the role. It keeps you fresh in their minds and shows your enthusiasm.
✨Tip Number 4
Apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re proactive and genuinely interested in joining our team at CRO Solutions.
We think you need these skills to ace Clinical Trials Administrator - (Maternity Cover) in Salford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Trials Administrator role. Highlight your relevant experience, especially any clinical trial work you've done, and showcase your organisational skills. 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 explain why you're passionate about clinical trials and how your background makes you the perfect fit for this maternity cover position. Keep it engaging and personal – we love a bit of personality!
Showcase Your Skills: Don’t forget to mention your IT skills, especially with MS Office, as well as your understanding of ICH GCP. We’re looking for someone who can ensure data integrity and patient safety, so make sure these skills are front and centre 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. Plus, it shows you’re keen to join our team!
How to prepare for a job interview at CRO-Solutions®, an IQVIA business
✨Know Your Clinical Trials Inside Out
Make sure you brush up on your clinical trial knowledge before the interview. Understand the phases of trials, data integrity, and patient safety protocols. Being able to discuss these topics confidently will show that you're not just familiar with the role but genuinely passionate about it.
✨Show Off Your Organisational Skills
As a Clinical Trials Administrator, organisation is key. Prepare examples from your past experience where you've successfully managed multiple tasks or projects. This could be anything from site selection to data management. Highlighting your ability to juggle responsibilities will impress the interviewers.
✨Demonstrate Team Spirit
Even though this role requires independence, being part of a team is crucial. Be ready to share experiences where you've collaborated effectively with others. Discuss how you’ve contributed to a team’s success in previous roles, especially in a clinical setting.
✨Prepare for Technical Questions
Expect questions related to ICH GCP guidelines and drug development processes. Brush up on your IT skills too, particularly with MS Office, as they may ask about your proficiency. Showing that you’re technically savvy will give you an edge over other candidates.