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- Tasks: Coordinate clinical trials and engage with pregnant participants to support groundbreaking research.
- Company: Leading healthcare organisation dedicated to advancing maternal health.
- Benefits: Competitive salary, flexible hours, and opportunities for professional growth.
- Why this job: Make a real difference in the lives of pregnant women through impactful research.
- Qualifications: Must have midwifery or obstetric experience and strong communication skills.
- Other info: Join a passionate team in a supportive and dynamic environment.
The predicted salary is between 30000 - 40000 £ per year.
We are currently seeking a Clinical Research Coordinator with a background in midwifery or obstetrics to support clinical trials involving pregnant women. This role is ideal for someone with hands-on experience screening and engaging pregnant participants, combined with a solid understanding of clinical trial processes.
Key requirements:
- Midwifery or obstetric clinical experience (MUST HAVE)
- Experience screening and supporting pregnant women in a research or clinical setting
- Strong attention to detail and patient-focused communication skills
Clinical Research Coordinator in Cornwall employer: Actalent
Contact Detail:
Actalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Coordinator in Cornwall
✨Tip Number 1
Network like a pro! Reach out to your connections in the midwifery and obstetrics fields. Attend relevant events or webinars where you can meet potential employers or colleagues who might know of openings.
✨Tip Number 2
Show off your hands-on experience! When you get the chance to chat with recruiters or during interviews, highlight specific examples of how you've screened and engaged pregnant participants in past roles.
✨Tip Number 3
Brush up on your clinical trial knowledge! Make sure you're familiar with the latest processes and regulations in clinical research. This will help you stand out as someone who’s not just experienced but also knowledgeable.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities that match your skills. Plus, applying directly shows your enthusiasm and commitment to joining our team.
We think you need these skills to ace Clinical Research Coordinator in Cornwall
Some tips for your application 🫡
Show Off Your Experience: Make sure to highlight your midwifery or obstetric experience right at the start. We want to see how your hands-on experience with pregnant participants makes you a perfect fit for this role!
Be Detail-Oriented: Since attention to detail is key, double-check your application for any typos or errors. We appreciate clear and precise communication, so let’s make sure your application reflects that!
Tailor Your Application: Don’t just send a generic application! We love it when candidates tailor their CV and cover letter to match the job description. Show us how your skills align with our needs in clinical trials.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Actalent
✨Know Your Stuff
Make sure you brush up on your midwifery and obstetrics knowledge. Be ready to discuss specific clinical trial processes and how they relate to working with pregnant women. This shows that you’re not just familiar with the theory but can apply it in real-world scenarios.
✨Showcase Your Experience
Prepare examples from your past roles where you successfully screened and engaged pregnant participants. Use the STAR method (Situation, Task, Action, Result) to structure your answers, making it easy for the interviewer to see your impact.
✨Communicate Clearly
Since strong patient-focused communication skills are key, practice explaining complex concepts in simple terms. You might be asked how you would communicate trial information to participants, so think about how you can make it relatable and understandable.
✨Attention to Detail is Key
Be prepared to discuss how you ensure accuracy in your work. Whether it’s data entry or participant screening, share specific strategies you use to maintain high standards. This will demonstrate your commitment to quality in clinical research.