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Clinical Research Assistant

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Actalent

13d ago

  • Job
    Full-time
    Entry & Junior Level
  • Research & Development
    Healthcare
  • Cleveland

AI generated summary

  • You need experience in data entry, regulatory documentation, scheduling studies, processing lab specimens, and strong organizational skills for administrative tasks.
  • You will verify research data, input information into EDC and CTMS, maintain files, schedule visits, process lab specimens, and perform administrative tasks to support studies effectively.

Requirements

  • Job Requirements:
  • 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

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.

What are the main responsibilities of a Clinical Research Assistant?

The main responsibilities include verifying research study information, inputting data into Electronic Data Capture (EDC) systems, preparing study files, maintaining regulatory documentation, scheduling subject visits, processing lab specimens, and performing various administrative support functions.

What type of employment is this position?

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

Is this a good opportunity for someone looking to work in a large CRO?

Yes, this position offers a great opportunity to work with a large CRO.

What qualifications are required for the Clinical Research Assistant role?

While specific qualifications are not listed in the job description, candidates generally need a background in clinical research, attention to detail, and strong organizational skills.

Are there opportunities for growth within the company?

Yes, Actalent emphasizes ensuring growth opportunities for their people.

What does Actalent believe about diversity, equity, and inclusion?

Actalent believes that diversity and inclusion are essential for the equity and success of their people and work to embed DE&I into their culture.

How can I request a reasonable accommodation due to a disability?

You can request a reasonable accommodation by emailing actalentaccommodation@actalentservices.com for other accommodation options.

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.