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Clinical Trial Assistant I

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Actalent

3mo ago

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

AI generated summary

  • You must assist in managing Phase I trials, perform vitals, collect samples, ensure dietary compliance, maintain records, uphold participant safety and confidentiality, and support study procedures.
  • You will assist with Phase I trials, perform vital sign checks, collect samples, monitor dietary compliance, prepare rooms, maintain records, ensure participant safety, and address complaints effectively.

Requirements

  • Will work with Clinical Research Nurses and Clinical Research Coordinators to manage Phase I Clinical Trials.
  • Accurately perform blood pressure, venipuncture, weights, pulse, respiratory rate, and temperature readings.
  • Preparation and accurate recording of ECGs/Holters.
  • Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples.
  • Monitors meals to ensure dietary compliance by research participants.
  • Assist in the preparation of rooms and medical equipment.
  • Assist with screening procedures as needed.
  • Maintain a clean, safe and efficient working and study environment.
  • Build respectful relationships with study participants.
  • Accurately record all research data obtained or observed.
  • Assist with QC of source documents and case report forms.
  • Maintains a basic understanding of current regulatory requirements.
  • Attends all required meetings, as appropriate.
  • Assists, as necessary, with study procedures.
  • Maintains accurate records of all work undertaken.
  • Maintains skills to perform all study tasks, as required.
  • Maintains constant awareness of participant safety and dignity at all times.
  • Handles participant complaints efficiently and effectively in order that their satisfaction is maintained.
  • Ensures that client and participant confidentiality is maintained.
  • Responds to client and team queries in a timely manner.
  • Takes ownership for the quality and standard of own work.

Responsibilities

  • Will work with Clinical Research Nurses and Clinical Research Coordinators to manage Phase I Clinical Trials.
  • Accurately perform blood pressure, venipuncture, weights, pulse, respiratory rate, and temperature readings.
  • Preparation and accurate recording of ECGs/Holters.
  • Collection and processing of biological samples as specified in the protocol and ensures the proper distribution of those samples.
  • Monitors meals to ensure dietary compliance by research participants.
  • Assist in the preparation of rooms and medical equipment.
  • Assist with screening procedures as needed.
  • Maintain a clean, safe and efficient working and study environment.
  • Build respectful relationships with study participants.
  • Accurately record all research data obtained or observed.
  • Assist with QC of source documents and case report forms.
  • Maintains a basic understanding of current regulatory requirements.
  • Attends all required meetings, as appropriate.
  • Assists, as necessary, with study procedures.
  • Maintains accurate records of all work undertaken.
  • Maintains skills to perform all study tasks, as required.
  • Maintains constant awareness of participant safety and dignity at all times.
  • Handles participant complaints efficiently and effectively in order that their satisfaction is maintained.
  • Ensures that client and participant confidentiality is maintained.
  • Responds to client and team queries in a timely manner.
  • Takes ownership for the quality and standard of own work.

FAQs

What shifts will I be working as a Clinical Trial Assistant I?

This role will involve rotating through three shifts, including a weekend shift every other week. Start times can vary between the first shift (5 AM to 7 AM), second shift (2 PM to 4 PM), and third shift (10 PM to 12 Midnight).

Will I need any specific skills or qualifications for this position?

Yes, candidates should have basic skills in performing blood pressure checks, venipuncture, weight measurements, pulse and respiratory rate assessments, and temperature readings. A basic understanding of current regulatory requirements is also beneficial.

Is there any opportunity for growth within the company?

Actalent is committed to providing growth opportunities for its employees, fostering a culture of care, engagement, and recognition.

How does Actalent ensure participant confidentiality?

Actalent ensures that client and participant confidentiality is maintained by adhering to strict protocols and handling all information with the utmost care and privacy.

Will I receive training for this role?

Yes, necessary training will be provided to maintain and develop skills required to perform all study tasks competently.

What is the process for addressing participant complaints?

Participants' complaints will be handled efficiently and effectively to ensure their satisfaction is maintained, reflecting the commitment to participant safety and dignity.

How are schedules determined for this position?

Schedules are typically set 2-3 weeks in advance, allowing for planning and flexibility within the rotating shifts.

Is there an emphasis on diversity and inclusion within the company?

Yes, diversity, equity, and inclusion are integral components of Actalent's culture, focusing on hiring diverse talent and maintaining an inclusive environment.

Will I be working closely with other team members?

Yes, you will be working alongside Clinical Research Nurses and Clinical Research Coordinators in managing Phase I Clinical Trials.

How do I apply for this position?

You can apply for the position through Actalent's application process as outlined on their careers page, and if you need any accommodations for the application or interview process, you can email actalentaccommodation@actalentservices.com.

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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.