At a Glance
- Tasks: Support clinical research studies and ensure participant safety while maintaining study documentation.
- Company: Join IQVIA, a leader in the clinical research industry.
- Benefits: Flexible part-time hours, remote work options, and valuable experience in clinical research.
- Other info: Short-term role with opportunities to develop skills and network in the industry.
- Why this job: Make a difference in healthcare while gaining hands-on experience in clinical trials.
- Qualifications: Degree in life sciences or relevant experience in a clinical setting required.
The predicted salary is between 15 - 20 £ per hour.
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 is currently looking for a Clinical Research Coordinator/Site Research Assistant to support a clinical study. This is a short-term study assignment (6 months), working 13 hours per week, supporting a site in Blackburn. The role is one day onsite and half a day remote each week.
Key Responsibilities
- Support clinical research studies and maintain a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.
- Safeguard the well-being of study participants, act as a patient advocate, and address participant concerns.
- Maintain up-to-date study documentation, including study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other essential records.
- Plan and coordinate logistical activities for study procedures in line with the study protocol.
- Perform clinical study set-up and preparation, including labeling specimen collection tubes and containers, managing inventory of required supplies, and setting up or troubleshooting study equipment.
- Assist with data entry, data quality checks, and query resolution to ensure protocol compliance and data accuracy.
- Support study enrollment activities, including recruiting, screening, and orienting participants according to the study protocol.
- Ensure correct custody and handling of study medication in accordance with site standard operating procedures.
- Coordinate with study monitors on study-related issues and respond effectively to monitor-initiated queries.
- Perform and document patient vital signs.
Required Skills And Experience
- BS/BA in life sciences or equivalent education and/or relevant work experience in a clinical or medical setting (e.g., Clinical Research Coordinator, Research Nurse, Medical Assistant, or similar role).
- Ideally an experienced Research Nurse or a highly experienced Clinical Research Coordinator/Site Research Assistant.
- Strong knowledge of clinical trials, including departmental, protocol-specific, and study-specific operating procedures, consent forms, and study schedules.
- Strong IT skills, with proficiency in MS Windows and Microsoft Office applications (Access, Outlook, Excel, Word).
- Excellent interpersonal skills with the ability to build and maintain effective working relationships with colleagues, managers, and clients.
- Strong organizational skills with close attention to detail.
Hybrid Clinical Research Coordinator – 6-Month, Part-Time employer: IQVIA
At IQVIA, we pride ourselves on being an industry leader in clinical research, offering a supportive and collaborative work environment that fosters professional growth. Our part-time Hybrid Clinical Research Coordinator role in Blackburn provides flexibility with a blend of onsite and remote work, allowing you to balance your career with personal commitments while contributing to meaningful research that impacts patient care. Join us to be part of a team that values innovation, integrity, and the well-being of our study participants.
StudySmarter Expert Advice🤫
We think this is how you could land Hybrid Clinical Research Coordinator – 6-Month, Part-Time
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and the role. Understand their values and how they align with your skills. This will help you stand out and show that you're genuinely interested in joining their team.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to clinical trials and participant care. Being well-prepared will boost your confidence and help you articulate your experience effectively.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Hybrid Clinical Research Coordinator – 6-Month, Part-Time
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Coordinator role. Highlight relevant experience and skills that match the job description, like your knowledge of clinical trials and any previous roles in a medical setting.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your background makes you a great fit for the team. Don’t forget to mention your strong interpersonal skills!
Showcase Your IT Skills:Since strong IT skills are essential for this role, make sure to mention your proficiency in MS Office applications. If you've used any specific software related to clinical trials, be sure to include that too!
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and get you one step closer to joining our team!
How to prepare for a job interview at IQVIA
✨Know Your Stuff
Make sure you brush up on clinical research basics and the specific responsibilities of a Clinical Research Coordinator. Familiarise yourself with common protocols, case report forms, and data management systems. This will show that you're not just interested in the role but also understand what it entails.
✨Showcase Your Experience
Prepare to discuss your relevant experience in detail. Whether it's your time as a Research Nurse or any other related role, be ready to share specific examples of how you've handled patient interactions, data management, or logistical planning. This will help demonstrate your capability and fit for the position.
✨Ask Smart Questions
Interviews are a two-way street, so come armed with thoughtful questions about the study, team dynamics, and company culture. This not only shows your interest but also helps you gauge if the company is the right fit for you.
✨Be Organised and Professional
Since this role requires strong organisational skills, make sure your interview materials are well-prepared. Bring copies of your CV, a list of references, and any certifications. Dress professionally, even if part of the job is remote, as first impressions matter!
