Site Research Assistant

IQVIA; High Wycombe; On-site; GBP 25,000 - 40,000; Part time

Job summary

An established industry player is seeking a motivated Research Assistant to join their High Wycombe site. This part-time role involves supporting clinical trials through various administrative tasks, ensuring compliance with protocols, and safeguarding participant well-being. Ideal candidates will possess a background in life sciences and have strong interpersonal and organizational skills. This position offers a unique opportunity to contribute to impactful research in a collaborative environment. If you are passionate about clinical research and eager to make a difference, this role is perfect for you.

Qualifications

• Experience in a clinical environment or medical setting.
• Basic knowledge of clinical trials and medical terminology.

Responsibilities

• Support clinical research studies and maintain safety protocols.
• Assist with data entry and quality checking for study accuracy.

Skills

Clinical Research Knowledge

Interpersonal Skills

Organizational Skills

IT Competence (MS Office)

Attention to Detail

Education

BS/BA in Life Sciences

Relevant Work Experience

Tools

MS Windows

MS Office (Access, Outlook, Excel, Word)

Job description

IQVIA High Wycombe, England, United Kingdom

Site Research Assistant

IQVIA High Wycombe, England, United Kingdom

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Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Research Assistant.

This part-time (24 hours) role is to support a site in High Wycombe and you will need to be onsite for all working hours.

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.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Health Care Provider, Administrative, and Research

• Industries

  Research Services

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