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Clinical Research Assistant

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Actalent

13d ago

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

AI generated summary

  • You should verify research data, input info into EDC and CTMS, maintain files, assist with regulatory docs, schedule visits, process lab specimens, and perform administrative tasks.
  • You will verify study data, input information into EDC and CTMS, maintain files, manage regulatory docs, schedule visits, process lab specimens, and handle administrative tasks.

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 are the primary responsibilities of a Clinical Research Assistant?

The primary responsibilities include verifying research study information, inputting data into EDC systems, maintaining research study files, compiling and submitting study information, assisting in regulatory documentation, scheduling subject visits, tracking patient visits in CTMS, processing lab specimens, and performing various administrative support functions.

What is the duration of the contract position?

The contract position is for a duration of 5 months.

Is there an opportunity for career growth in this position?

Yes, there are growth opportunities as Actalent is committed to ensuring the development and recognition of its employees.

What qualifications are required to apply for this Clinical Research Assistant position?

While specific qualifications may not be detailed in the job description, typically a background in life sciences or related fields is preferred, along with strong organizational and data management skills.

What platforms or systems will I be using in this role?

You will be using Electronic Data Capture (EDC) systems and a Clinical Trial Management System (CTMS) for tracking patient visits and procedures.

How does Actalent ensure diversity and inclusion in the workplace?

Actalent fosters diversity and inclusion through hiring diverse talent, maintaining an inclusive environment, building a culture of care and engagement, and providing growth opportunities for all employees.

What should I do if I need a reasonable accommodation during the application process?

If you need a reasonable accommodation, please email actalentaccommodation@actalentservices.com for assistance with the job application or interviewing 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.