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Clinical Research Assistant

  • Job
    Full-time
    Entry, Junior & Mid Level
  • Research & Development
    Healthcare
  • Lafayette, +1

AI generated summary

  • You should have basic clinical trial knowledge, familiarity with protocols and procedures, and experience in patient recruitment and EDC data entry/query resolution.
  • You will verify study data, input information into EDC systems, maintain research files, manage regulatory documents, and schedule subject visits while ensuring quality and deadlines are met.

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 research study information, inputting data into the Electronic Data Capture (EDC) system, preparing and maintaining study files, compiling and submitting study information, assisting in regulatory documentation maintenance, and scheduling subject visits.

What qualifications are necessary to apply for the Clinical Research Assistant position?

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

What is the role of a Clinical Research Assistant in the context of clinical trials?

A Clinical Research Assistant supports the execution of clinical trials by performing administrative tasks and assisting in clinical procedures to gather data on patients enrolled in or seeking enrollment in clinical studies.

Is prior experience in clinical research required for this position?

While prior experience in clinical research is beneficial, the position primarily requires knowledge and familiarity with clinical trials and specific operational procedures as outlined in the qualifications.

What kind of work environment can a Clinical Research Assistant expect?

A Clinical Research Assistant can expect a collaborative work environment focused on supporting clinical studies, with a culture that emphasizes diversity, equity, and inclusion.

Where can I find information about Actalent’s commitment to diversity and inclusion?

Information about Actalent's commitment to diversity, equity, and inclusion can be found on their website, where they detail their hiring practices, inclusive environment, and growth opportunities for employees.

How can I request accommodations during the application process?

If you need to request a reasonable accommodation due to a disability during the application or interviewing process, please email actalentaccommodation@actalentservices.com for assistance.

Does this position require frequent travel?

The job description does not specify travel requirements, but scheduling subject visits may involve some level of coordination which could entail travel depending on the study's needs.

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.