At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical trial protocols.
- Company: IQVIA is a top global provider of clinical research services, recognised for innovation in healthcare.
- Benefits: Enjoy a mix of remote and on-site work, plus genuine career development opportunities.
- Other info: This role requires flexibility for nationwide travel; UK Visa Sponsorship not available.
- Why this job: Make a real impact on patient outcomes while working with cutting-edge medicines.
- Qualifications: Over 2 years of independent monitoring experience and hands-on oncology expertise required.
The predicted salary is between 36000 - 60000 £ per year.
Reading, United Kingdom | Full time | Field-based | R1521358
Join IQVIA on our mission to accelerate innovation for a healthier world!
Why IQVIA?
- Career development opportunities to grow as we grow
- AI‑powered career advancement through our internal talent marketplace, Career Connections
- Mentorship opportunities across the organisation via Employee Resource Groups
- Flexible working to assist work–life balance and professional success
- Well‑being support covering your physical, mental, and financial health
Responsibilities
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
- Collaborate and liaise with study team members for project execution support as appropriate
Requirements
- Requires at least 2 years on-site monitoring experience of interventional studies
- Degree in scientific discipline or health care or equivalent industry experience
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Ability to establish and maintain effective working relationships with coworkers and clients
- Full UK right to work required, this position is not eligible for visa sponsorship
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Clinical Research Associate II in Reading employer: IQVIA Argentina
At IQVIA, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our Reading location offers a hybrid working model, allowing for flexibility while engaging in meaningful projects that impact clinical outcomes globally. We are committed to employee growth, providing ample opportunities for professional development and mentorship, making it an ideal place for those looking to advance their careers in clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate II in Reading
✨Tip Number 1
Familiarise yourself with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to maintaining high standards in clinical research.
✨Tip Number 2
Network with professionals in the clinical research field, especially those who have experience as Clinical Research Associates. Engaging with them can provide insights into the role and may even lead to referrals or recommendations for positions at IQVIA.
✨Tip Number 3
Highlight your experience in managing multiple clinical trial protocols during conversations or networking events. This is a key requirement for the role, and showcasing your ability to handle diverse investigative sites will set you apart from other candidates.
✨Tip Number 4
Stay updated on the latest developments in oncology, as hands-on experience in this therapeutic area is crucial for the position. Being knowledgeable about current trends and breakthroughs can give you an edge in discussions with hiring managers.
We think you need these skills to ace Clinical Research Associate II in Reading
Some tips for your application 🫡
Understand the Role:Before applying, make sure you fully understand the responsibilities and requirements of the Clinical Research Associate II position. Familiarise yourself with the key tasks such as site monitoring visits and compliance with GCP guidelines.
Tailor Your CV:Customise your CV to highlight relevant experience, especially your independent on-site monitoring experience and any work in the Oncology therapeutic area. Use specific examples that demonstrate your ability to manage clinical trial protocols.
Craft a Compelling Cover Letter:Write a cover letter that reflects your passion for advancing clinical research and improving patient outcomes. Mention why you want to work at IQVIA and how your skills align with their mission and values.
Proofread Your Application:Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application shows attention to detail, which is crucial in clinical research.
How to prepare for a job interview at IQVIA Argentina
✨Know Your GCP and ICH Guidelines
As a Clinical Research Associate, it's crucial to have a solid understanding of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Brush up on these regulations before your interview, as you may be asked to discuss how you've applied them in your previous roles.
✨Showcase Your Monitoring Experience
Highlight your independent on-site monitoring experience during the interview. Be prepared to share specific examples of how you've managed multiple clinical trial protocols and ensured compliance with regulatory requirements. This will demonstrate your capability and confidence in the role.
✨Discuss Your Oncology Knowledge
Since hands-on experience in the Oncology therapeutic area is essential for this position, make sure to discuss any relevant projects or studies you've worked on. This will show your familiarity with the field and your ability to contribute effectively to the team.
✨Emphasise Flexibility and Travel Commitment
This role requires nationwide travel, so it's important to express your flexibility and willingness to travel as needed. Share any past experiences where you've successfully managed travel commitments while maintaining work-life balance, as this will reassure the interviewer of your adaptability.
