Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you experience and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking Clinical Research Coordinator.

This role has an immediate start working 20 hours a week for a period of 6 months to support the site. The study coordinator should have experience clinically or nursing background as tasks includes perform EKG, collect vital signs.

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:

• Verifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collector

• Accurate input of trial data into the Electronic Data Capture (EDC) system and tracking visits and procedures completed against budget in the clinical trial management system (CTMS)

• Preparing and maintaining study files, and timely submission of information

• Collecting, submitting and assisting in maintaining relevant regulatory and ethics documents

• Scheduling visits with research subjects, generating appropriate reports and documentation

• Other administrative support functions such as reception, office organization and supply management.

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.

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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:

• Verifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collector

• Accurate input of trial data into the Electronic Data Capture (EDC) system and tracking visits and procedures completed against budget in the clinical trial management system (CTMS)

• Preparing and maintaining study files, and timely submission of information

• Collecting, submitting and assisting in maintaining relevant regulatory and ethics documents

• Scheduling visits with research subjects, generating appropriate reports and documentation

• Other administrative support functions such as reception, office organization and supply management.

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.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.

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