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Clinical Research Assistant

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Actalent

Today

  • Job
    Full-time
    Entry Level
  • Research & Development
    Healthcare
  • Oklahoma City

AI generated summary

  • You should verify study info, manage EDC/CTMS data, prepare files, handle regulatory docs, schedule visits, process lab specimens, and provide administrative support.
  • You will verify study data, input information into EDC systems, maintain files, schedule visits, process lab specimens, and perform administrative tasks to support research activities.

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 primary responsibilities of a Clinical Research Assistant?

Responsibilities include verifying research study information, inputting data into the EDC system, maintaining study files, scheduling subject visits, processing lab specimens, and performing various administrative support functions.

What type of job is this?

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

Is this position with a specific company?

Yes, this position is with Actalent, a global leader in engineering and sciences services and talent solutions.

What qualifications are needed for this role?

While specific qualifications are not mentioned in the job description, candidates typically need a background in clinical research, strong organizational skills, and proficiency in data entry.

Are there opportunities for growth within Actalent?

Yes, Actalent emphasizes ensuring growth opportunities for their people as part of their diversity, equity, and inclusion initiatives.

What is the work environment like?

The work environment is supportive and inclusive, as Actalent values diversity and aims to build a culture of care, engagement, and recognition.

How does Actalent address diversity and inclusion?

Actalent addresses diversity and inclusion by hiring diverse talent, maintaining an inclusive environment, and providing growth opportunities for all employees.

Can I request accommodations during the application or interview process?

Yes, candidates can request reasonable accommodations by emailing actalentaccommodation@actalentservices.com.

Is there an equal opportunity employment policy?

Yes, Actalent is an equal opportunity employer and considers all applications without regard to any characteristic protected by law.

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.