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Clinical Research Assistant

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Actalent

15d ago

  • Job
    Full-time
    Entry Level
  • Research & Development
    Healthcare
  • Monroe

AI generated summary

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

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 qualifications are required for the Clinical Research Assistant position?

The job description does not specify required qualifications, but typically, candidates should have a background in life sciences or a related field, as well as strong organizational and communication skills.

Is this a full-time or part-time position?

This is a contract position with a duration of 5 months, which may involve full-time hours depending on the study's requirements.

What are the main responsibilities of a Clinical Research Assistant?

The main responsibilities include verifying research study information, inputting data into EDC systems, preparing study files, scheduling subject visits, processing lab specimens, and performing various administrative support functions.

Is there an opportunity for growth in this position?

Yes, Actalent emphasizes growth opportunities for employees as part of their culture of care and engagement.

What is the work environment like at Actalent?

Actalent fosters a diverse and inclusive environment, focusing on equity and success for all employees through self-reflection and recognition.

Can individuals with disabilities apply for this position?

Yes, Actalent is an equal opportunity employer and encourages applications from all individuals, including those with disabilities. Reasonable accommodations can be requested during the application and interview process.

How can I apply for the Clinical Research Assistant position?

Interested candidates can submit their applications through Actalent's website or other job posting platforms where the position is advertised.

Are there any specific software systems the Clinical Research Assistant is expected to use?

Yes, familiarity with Electronic Data Capture (EDC) systems and Clinical Trial Management Systems (CTMS) is required for tracking data and subject visits.

What type of training will be provided for this position?

The job description does not specify training; however, Actalent usually provides onboarding and training relevant to the tasks and systems used in clinical trials.

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.