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Clinical Research Assistant

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Actalent

Today

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

AI generated summary

  • You must have basic clinical trial knowledge, understand protocols and procedures, and have experience in patient recruitment and EDC data entry/query resolution.
  • You will verify study data, input information into EDC systems, maintain files, submit reports, assist with regulatory docs, and schedule subject visits while ensuring data accuracy.

Requirements

  • Basic knowledge of clinical trials
  • In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
  • Experience with Patient recruitment, EDC data entry/query resolution required

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.

FAQs

What are the primary responsibilities of a Clinical Research Assistant?

The primary responsibilities include verifying and correcting research study information, inputting data into the Electronic Data Capture (EDC) system, preparing and maintaining research study files, compiling study information within deadlines, assisting with regulatory documentation, and scheduling subject visits.

What qualifications are required for this position?

Candidates should have a basic knowledge of clinical trials, in-depth knowledge of departmental and study-specific operating procedures, and experience with patient recruitment, EDC data entry, and query resolution.

Is previous experience in clinical trials necessary?

While a basic knowledge of clinical trials is required, specific previous experience may enhance your application, especially in areas like patient recruitment and data management.

What type of documentation will I be handling?

You will be responsible for maintaining regulatory documentation and research study files, including consent forms and study schedules.

Is there an opportunity for growth within the company?

Yes, Actalent emphasizes providing growth opportunities for its employees and building a culture of care and recognition.

How does Actalent support diversity, equity, and inclusion?

Actalent's DE&I initiatives include hiring diverse talent, maintaining an inclusive environment, and ensuring growth opportunities for all employees.

What is the process to request a reasonable accommodation?

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

Are there any specific software or systems I need to be familiar with for this role?

Familiarity with Electronic Data Capture (EDC) systems is required, as well as a general understanding of data entry processes.

Who can I contact for more information about the job?

For more detailed information about the job, you can reach out to the HR department or the contact person listed in the job posting if available.

Is this a full-time position?

The job description does not specify, so please check the application details or confirm with the hiring manager for clarity on the position's hours.

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.