Clinical Research Coordinator

IQVIA; Wolverhampton; On-site; GBP 25,000 - 35,000; Part time

Job summary

A leading global provider in clinical research is looking for a part-time Clinical Research Coordinator in Wolverhampton. The role involves supporting clinical trials, ensuring a safe study environment, and assisting with data management. Candidates should have a relevant degree in life sciences and experience in a clinical setting. Key responsibilities include safeguarding subjects, maintaining study protocols, and coordinating logistical activities. This position offers a unique opportunity to contribute to improving patient outcomes and advancing medical treatments.

Qualifications

• Relevant work experience in a clinical environment or medical setting.
• Knowledge of departmental, protocol, and study-specific operating procedures.
• Ability to pay close attention to detail.

Responsibilities

• Support clinical research studies and maintain a safe study environment.
• Safeguard the well-being of subjects and address their concerns.
• Assist with data entry, quality checking, and study enrollment.

Skills

Basic knowledge of clinical trials

Excellent interpersonal skills

Organizational skills

Strong IT competence

Education

BS/BA in life sciences or equivalent experience

Tools

MS Office (Excel, Word, Access)

Job description

Clinical Research Coordinator -Wolverhampton, UK page is loaded## Clinical Research Coordinator -Wolverhampton, UKlocations: Wolverhampton, England, United Kingdomtime type: Part timeposted on: Posted Todayjob requisition id: R1527749This part-time (24 hours) role is to support a site in **Wolverhampton** in conducting a clinical trial.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.#LI-DNP#LI-HCPN#LI-CES#LI-CT1IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more atIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.