Site Research Assistant - Falmouth, Cornwall

IQVIA; England; On-site; GBP 30,000 - 40,000; Part time

Job summary

A leading clinical research company is seeking a Site Research Assistant in Falmouth, Cornwall. This role involves supporting a clinical research study and maintaining an effective research environment with 24 hours per week. Candidates should possess a BS/BA in life sciences and at least 2 years of clinical research experience. Key responsibilities include managing study protocols, supporting patient enrolment, and conducting data entry. This is an excellent opportunity for individuals looking to contribute to clinical trials.

Qualifications

• Must have at least 2 years of experience as a Clinical Research Assistant or Coordinator.
• Good knowledge of clinical trials and study protocols.
• Basic knowledge of medical terminology.

Responsibilities

• Maintain study protocols, CRFs, and EDC systems.
• Support with patient enrolment and document collection.
• Perform data entry and quality checking.
• Manage biological samples and perform ECGs.
• Coordinate with study monitor on issues.

Skills

Knowledge of clinical trials

Interpersonal skills

Organizational skills

IT competence

Education

BS/BA in life sciences or equivalent

At least 2 years as Clinical Research Assistant

Tools

MS Office (Access, Outlook, Excel, Word)

Job description

Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Site Research Assistant to support a site in Falmouth, Cornwall.

This role with an immediate start is for 24 hours per week and is expected to last around one year. Working day will be Friday.

The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including:

• Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
• Support with screening and enrolment of patients and collection of related documents (informed consent, privacy consent, etc.);
• Planning and coordinating logistical activity for study procedures according to the study protocol
• Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
• Management and shipment of biological samples
• Performing ECG, taking vital signs, phlebotomy
• Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions
• Administrative research task

We are looking for candidates with:

• 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, Research Assistant, nurse, medical assistant, other medical profession
• Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
• Must have at least 2 years experience working as a Clinical Research Assistant or Clinical Research Coordinator at a clinical trial site
• 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 clients
• Good organizational skills with the ability to pay close attention to detail

If this sounds like the perfect opportunity for you, please apply now!

IQVIA 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 at https://jobs.iqvia.com