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- Tasks: Support clinical trials, manage data, and ensure participant safety in a dynamic environment.
- Company: Join IQVIA, a leader in clinical research, making a real impact in healthcare.
- Benefits: Part-time hours, flexible schedule, and the chance to gain valuable experience in the medical field.
- Why this job: Be part of groundbreaking research while developing skills in a supportive team culture.
- Qualifications: BS/BA in life sciences or relevant experience; strong IT and interpersonal skills required.
- Other info: This is a 6-month role based in Bristol, perfect for students seeking hands-on experience.
The predicted salary is between 24000 - 36000 £ per year.
Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company? If so, come and join us - IQVIA are looking for a Clinical Research Coordinator. This part-time (15 hours) role is planned for 6 months and is to support the site in Bristol in conducting a clinical trial in the field of Respiratory.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
Day to day responsibilities will include:
- Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator.
- Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns.
- Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
- Plan and coordinate logistical activity for study procedures according to the study protocol.
- Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues.
- Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness.
- Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol.
- Correct custody of study drug according to site standard operating procedures.
- Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
We are looking for candidates with the following skills and experience:
- BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession.
- Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules.
- Basic knowledge of medical terminology.
- Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word.
- Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients.
- Good organizational skills with the ability to pay close attention to detail.
Clinical Research Coordinator employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Coordinator
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in clinical research. This will not only help you understand the role better but also demonstrate your commitment to staying updated in this fast-paced field.
✨Tip Number 2
Network with professionals in the clinical research community. Attend relevant workshops, webinars, or local meetups to connect with others in the field, which can lead to valuable insights and potential referrals.
✨Tip Number 3
Gain hands-on experience by volunteering or interning in a clinical setting. This practical exposure will enhance your understanding of clinical trials and make you a more attractive candidate for the role.
✨Tip Number 4
Prepare for the interview by practising common questions related to clinical research coordination. Be ready to discuss your experiences and how they align with the responsibilities outlined in the job description.
We think you need these skills to ace Clinical Research Coordinator
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research or related fields. Emphasise any roles where you've supported clinical trials, managed data, or worked with medical professionals.
Craft a Compelling Cover Letter: Write a cover letter that specifically addresses the responsibilities and skills mentioned in the job description. Explain why you're passionate about clinical research and how your background makes you a great fit for the role.
Highlight Relevant Skills: In your application, focus on your organisational skills, attention to detail, and IT competence. Mention specific software you are proficient in, such as MS Office applications, and any experience with data entry or quality checking.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a Clinical Research Coordinator.
How to prepare for a job interview at IQVIA
✨Know Your Clinical Research Basics
Make sure you brush up on your knowledge of clinical trials and the specific protocols related to the role. Being able to discuss these topics confidently will show that you're well-prepared and genuinely interested in the position.
✨Highlight Relevant Experience
Be ready to share specific examples from your past work or studies that demonstrate your skills in a clinical environment. Whether it's your experience as a clinical research coordinator or any relevant medical profession, make those connections clear.
✨Showcase Your IT Skills
Since the role requires strong IT competence, be prepared to discuss your experience with MS Office applications, especially Excel and Access. You might even want to mention any specific projects where you've used these tools effectively.
✨Demonstrate Interpersonal Skills
As a Clinical Research Coordinator, you'll need to work closely with various stakeholders. Be ready to talk about how you've built effective working relationships in the past and how you handle communication with team members and volunteers.
