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For Companies At a Glance
- 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: Enjoy flexible part-time hours and gain valuable experience in the medical field.
- Why this job: Be part of groundbreaking research while developing essential skills in a supportive team culture.
- Qualifications: A degree in life sciences or relevant experience in a clinical setting is required.
- Other info: This role is perfect for those passionate about healthcare and research.
The predicted salary is between 24000 - 36000 £ per year.
Job Description
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 role is to support a site in Oldham in conducting a clinical trial for 16 hours per week.
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 client
- 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 already working in clinical research. Attend industry events or join online forums to connect with others in the field, as personal recommendations can significantly boost your chances of landing the job.
✨Tip Number 3
Prepare for potential interview questions by practising responses related to your understanding of clinical trials and your experience in a medical setting. Being able to articulate your knowledge clearly will set you apart from other candidates.
✨Tip Number 4
Showcase your organisational skills during the interview by discussing specific examples of how you've managed multiple tasks or projects in the past. This will highlight your ability to handle the responsibilities of a Clinical Research Coordinator effectively.
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 showcases your passion for clinical research and your understanding of the role. Mention specific skills that align with the job description, such as your knowledge of clinical trials and your organisational abilities.
Highlight Relevant Skills: In your application, clearly outline your IT competence, particularly with MS Office applications, and your interpersonal skills. Provide examples of how you've used these skills in previous roles to support clinical studies.
Proofread Your Application: Before submitting, carefully proofread your application 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 Trials
Familiarise yourself with the basics of clinical trials, including phases, protocols, and regulations. Being able to discuss these topics confidently will show your understanding of the role and its importance.
✨Highlight Relevant Experience
Prepare to discuss any previous experience in clinical settings or research roles. Be specific about your responsibilities and how they relate to the tasks outlined in the job description.
✨Demonstrate Attention to Detail
Since the role requires meticulous data entry and quality checking, be ready to provide examples of how you've ensured accuracy in your past work. This could include specific projects where attention to detail was crucial.
✨Showcase Your Interpersonal Skills
As a Clinical Research Coordinator, you'll need to work closely with various stakeholders. Prepare examples that demonstrate your ability to build relationships and communicate effectively with team members and participants.