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Clinical Research Assistant

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Actalent

17d ago

  • Internship
    Full-time
    Off-cycle Internship
  • Research & Development
    Healthcare
  • Norfolk

AI generated summary

  • You need basic clinical trial knowledge, medical terminology skills, EDC data entry experience, MS Office proficiency, and excellent interpersonal skills for patient recruitment.
  • You will verify study data, input information into EDC and CTMS, maintain files, schedule visits, process lab specimens, and provide administrative support.

Requirements

  • Basic knowledge of clinical trials
  • In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
  • Basic knowledge of medical terminology
  • Skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
  • Excellent interpersonal skills
  • Experience with Patient recruitment, EDC data entry/query resolution

Responsibilities

  • Verify and/or correct research study information on source documents. Research queries and variances, and provide feedback to the site data collector.
  • Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content, accuracy, and completeness.
  • Prepare and maintain research study files.
  • Compile, collate and submit study information within established deadlines.
  • Assist in maintenance of regulatory documentation.
  • Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits.
  • Input visit data into Clinical Trial Management System (CTMS) to track patient visits and procedures completed against the study budget.
  • Process required lab specimens, label vials, and accurately fill out requisitions for storage and/or shipment per the study protocol and packaging and shipment regulations.
  • Perform various administrative support functions such as reception, office organization, and office supply management.

FAQs

What is the job title for this position?

The job title is Clinical Research Assistant.

Where is this position located?

This position is on-site at multiple locations with a large Contract Research Organization (CRO).

What are the primary responsibilities of a Clinical Research Assistant?

Primary responsibilities include verifying research study information, inputting data into EDC systems, preparing research files, maintaining regulatory documentation, scheduling subject visits, and processing lab specimens, among others.

What kind of experience is required for this role?

Candidates should have experience with patient recruitment, EDC data entry, and query resolution.

What type of contract is offered for this position?

This is a contract position with a duration of 5 months.

What qualifications are needed for this position?

Basic knowledge of clinical trials, in-depth knowledge of operating procedures and consent forms, basic medical terminology knowledge, proficiency in MS Windows and Office applications, and excellent interpersonal skills are required.

Is training provided for this position?

The job description does not specify training, but a basic knowledge of clinical trials and medical terminology is expected, suggesting there may be some training involved.

What is the company culture regarding diversity?

Actalent values diversity and inclusion, implementing practices to hire diverse talent, maintain an inclusive environment, and ensure growth opportunities for employees.

Are there opportunities for career advancement within the company?

Yes, the company emphasizes growth opportunities for their people as part of their culture of care and engagement.

How can accommodations be requested for the application process?

If you need a reasonable accommodation due to a disability, you can email actalentaccommodation@actalentservices.com for assistance with the application or interview process.

Actalent

An Engineering and Sciences Services Company | People to Possible

Human Resources
Industry
5001-10,000
Employees

Mission & Purpose

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent’s global footprint and flexible delivery models ensure access to specialized talent where and when you need it. We promote consultant engagement through professional development and provide experiences to ensure continuous learning. Our people are the difference. Our expertise spans capabilities in engineering including product and manufacturing, systems and software, construction management, environmental, architecture and civil; and power and utilities. We focus on sciences capabilities in laboratory sciences, healthcare, and clinical research. Actalent is an operating company of Allegis Group, the global leader in talent solutions.