Site Research Assistant Torpoint, Cornwall

IQVIA; City Of London; On-site; GBP 20,000 - 30,000; Part time

Job summary

A leading global provider of clinical research services is seeking a Site Research Assistant for a part-time position in Torpoint, Cornwall. The role involves supporting clinical trials, managing study protocols, and performing administrative tasks. Candidates should have a BS/BA in life sciences or equivalent and at least 2 years of experience as a Clinical Research Assistant. Strong IT skills and the ability to work collaboratively are essential.

Qualifications

• At least 2 years experience as a Clinical Research Assistant or Coordinator.
• Good knowledge of clinical trials and departmental protocols.
• Strong IT competence with MS Office applications.

Responsibilities

• Support a clinical research study and maintain a safe study environment.
• Manage and ship biological samples.
• Perform ECG and take vital signs.

Skills

Laboratory Experience

Data Collection

Biochemistry

Statistical Software

Research Experience

Education

BS / BA in life sciences or equivalent

Tools

MS Windows

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 Torpoint 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

Key Skills

Laboratory Experience,Spss,Data Collection,DNA Isolation,Stata,Biochemistry,Qualitative Research Interviewing,Research Experience,Statistical Software,Molecular Biology,Research Laboratory Experience,Western Blot

Employment Type: Part-Time

Experience: years

Vacancy: 1