At a Glance
- Tasks: Monitor clinical trials, ensure compliance, and support site staff.
- Company: Join a leading client dedicated to innovative medical research.
- Benefits: Enjoy remote work, competitive salary, healthcare, PTO, and 401k.
- Why this job: Make a real impact on patients' lives while advancing your career.
- Qualifications: Bachelor's in Life Sciences or related field; 1+ years in clinical research preferred.
- Other info: Opportunity for travel and collaboration with cross-functional teams.
The predicted salary is between 28800 - 48000 £ per year.
Now Hiring: Clinical Research Associate (CRA)
Are you passionate about advancing medical research and ensuring clinical trials run smoothly? We’re looking for a Clinical Research Associate (CRA) to join our top client in the US and help bring innovative treatments to patients worldwide!
Location: Remote
Job Type: Permanent
About the Role:
As a Clinical Research Associate, you’ll play a crucial role in monitoring clinical trial sites, ensuring compliance with Good Clinical Practice (GCP) guidelines, and maintaining high-quality data integrity. You’ll work closely with investigators, site staff, and sponsors to make sure studies are conducted efficiently and ethically.
What You’ll Do:
- Monitor clinical trial sites to ensure protocol adherence and regulatory compliance
- Conduct site visits (remote and on-site) to oversee data collection and patient safety
- Train and support site staff on study procedures and regulatory requirements
- Verify Case Report Forms (CRFs) against source documents for accuracy
- Identify and address any issues that could impact study quality or timelines
- Ensure proper documentation and reporting of adverse events
- Collaborate with cross-functional teams, including project managers and regulatory affairs
What We’re Looking For:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field
- 1+ years of experience in clinical research (CRA, CTA, or study coordinator roles preferred)
- Strong knowledge of ICH-GCP, FDA, and other regulatory guidelines
- Excellent attention to detail and problem-solving skills
- Willingness to travel
- Strong communication and teamwork skills
Why our Client?
- Work on groundbreaking clinical trials that make a real impact on patients’ lives
- Career growth opportunities in a fast-paced, innovative environment
- Competitive salary + benefits (healthcare, PTO, 401k, etc.)
If you’re ready to take the next step in your clinical research career, we’d love to hear from you! Apply today: Eloise@greenlsr.com
Clinical Research Associate employer: Green Life Science
Contact Detail:
Green Life Science Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate
✨Tip Number 1
Network with professionals in the clinical research field. Attend industry conferences, webinars, or local meetups to connect with others who can provide insights and potentially refer you to job openings.
✨Tip Number 2
Familiarise yourself with the latest regulations and guidelines related to clinical trials, such as ICH-GCP and FDA requirements. This knowledge will not only boost your confidence but also demonstrate your commitment to the role during interviews.
✨Tip Number 3
Consider gaining additional certifications relevant to clinical research, such as a Clinical Research Coordinator (CRC) or Clinical Research Associate (CRA) certification. These credentials can set you apart from other candidates.
✨Tip Number 4
Prepare for potential interview questions by practising responses that highlight your experience in monitoring clinical trials and ensuring compliance. Use specific examples to illustrate your problem-solving skills and attention to detail.
We think you need these skills to ace Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research. Emphasise any roles you've had as a CRA, CTA, or study coordinator, and showcase your knowledge of ICH-GCP and FDA guidelines.
Craft a Compelling Cover Letter: Write a cover letter that reflects your passion for advancing medical research. Mention specific experiences that demonstrate your attention to detail and problem-solving skills, and explain why you want to work with this particular client.
Highlight Relevant Skills: In your application, clearly outline your strong communication and teamwork skills. Provide examples of how you've collaborated with cross-functional teams in previous roles, as this is crucial for the position.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors. A polished application shows professionalism and attention to detail, which are essential traits for a Clinical Research Associate.
How to prepare for a job interview at Green Life Science
✨Know Your Regulations
Familiarise yourself with ICH-GCP and FDA guidelines. Being able to discuss these regulations confidently will show your understanding of the clinical research landscape and demonstrate your commitment to compliance.
✨Highlight Relevant Experience
Prepare to discuss your previous roles in clinical research, especially any experience as a CRA, CTA, or study coordinator. Use specific examples to illustrate how you've contributed to successful trials and maintained data integrity.
✨Demonstrate Attention to Detail
Since this role requires high attention to detail, be ready to provide examples of how you've ensured accuracy in data collection and reporting in past positions. This will help convey your suitability for the role.
✨Showcase Communication Skills
As a CRA, you'll need to collaborate with various teams. Prepare to discuss how you've effectively communicated with investigators, site staff, and sponsors in the past, highlighting your teamwork and problem-solving abilities.