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Clinical Research Assistant

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Actalent

14d ago

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

AI generated summary

  • You should have basic clinical trial knowledge, familiarity with operating procedures, medical terminology, MS Office skills, excellent interpersonal abilities, and experience in patient recruitment and EDC data entry.
  • You will verify study data, input information into EDC systems, maintain files, schedule visits, manage lab specimens, and provide administrative support, ensuring compliance and accuracy throughout.

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 for this position is Clinical Research Assistant.

Is this position remote or on-site?

This position is on-site in multiple locations available.

What are the primary responsibilities of a Clinical Research Assistant?

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

What qualifications are required for this job?

Required qualifications include basic knowledge of clinical trials, medical terminology, proficiency in MS Windows and Office applications, and excellent interpersonal skills.

What type of employment is this position?

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

Who is the employer for this position?

The employer for this position is Actalent.

Is there an equal opportunity employment policy?

Yes, the company is an equal opportunity employer and considers all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information, or any characteristic protected by law.

How can I request accommodations during the application process?

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

Is experience with patient recruitment necessary for this role?

Yes, experience with patient recruitment, EDC data entry, and query resolution is preferred.

What skills are preferred for using data management systems?

Proficiency in using Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) systems is preferred for this role.

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.