Logo of Huzzle

Intern - Clinical Trial Assistant

image

Grifols

27d ago

  • Internship
    Full-time
    Summer Internship
  • Research & Development
    Healthcare
  • Durham

AI generated summary

  • You must be pursuing a Bachelor's degree in science (rising junior/senior) or a Master's/PhD with a GPA of 3.0 or higher.
  • You will assist with clinical trial operations, manage study supplies, track documentation, liaise with site staff, support meetings, develop study tools, and oversee the SPARTA project.

Requirements

  • Must be currently pursuing Bachelor's degree in a scientific field - rising junior or senior OR Master's or PhD student maintaining GPA of 3.0 or higher

Responsibilities

  • Become familiar in day-to-day operations of clinical trials and assist the needs of clinical sites, vendors, and the sponsor study team
  • Shipping and tracking of physical study supplies to/from clinical sites and third parties
  • Aid in production, tracking and analysis of Trial Master File documentation and inventories
  • Correspond with site staff (domestic and international)
  • Assist in the triage of study action items, taking minutes for meetings, and sending out eCDA requests
  • Assist in development and review study documents and tools
  • Assist with preparing Investigator Meetings (presentation, ordering of supplies, shipments, etc)
  • Responsible for SPARTA project

FAQs

What is the primary role of an intern in the Clinical Trial Assistant position?

The primary role of the intern is to provide support to several Grifols clinical trials, which includes familiarizing with day-to-day operations, assisting clinical sites, vendors, and the sponsor study team.

What educational background is required for this internship?

Candidates must be currently pursuing a Bachelor’s degree in a scientific field (rising junior or senior) or be Master's or PhD students maintaining a GPA of 3.0 or higher.

Where is the position located?

The position is located in North America, specifically at RTP, North Carolina, in the Research Building 85.

What types of tasks will the intern be responsible for?

Tasks include shipping and tracking study supplies, aiding in the production and analysis of Trial Master File documentation, corresponding with site staff, assisting in meetings, and helping in the development and review of study documents and tools.

Is previous experience in clinical trials required for this internship?

No previous experience in clinical trials is mentioned as a requirement, but familiarity with clinical trial operations may be beneficial.

Who should I contact if I want to apply through a recruiting agency?

Agencies must have an active, non-expired Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department and should submit candidates only as directed by a Grifols Recruiter.

What types of equal employment opportunities does Grifols provide?

Grifols provides equal employment opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic or status protected by law.

Are there any specific benefits offered for this internship position?

The job description does not specify benefits for the internship position; candidates might need to inquire directly with the hiring department for details.

What is the SPARTA project mentioned in the responsibilities?

The job description does not provide specific details about the SPARTA project; further clarification may be needed during the interview process.

How can I learn more about Grifols and its work in healthcare?

You can visit the Grifols website to learn more about their history, products, and commitment to improving healthcare worldwide.

Innovating for patients and society

Manufacturing & Electronics
Industry
10,001+
Employees
1909
Founded Year

Mission & Purpose

Grifols is a global healthcare company founded in Barcelona in 1909 committed to improving the health and well-being of people all over the world. A leader in essential plasma-derived medicines and transfusion medicine, we develop, produce and provide innovative healthcare services and solutions in more than 110 countries. Patient needs and our ever-growing knowledge of many chronic, rare and prevalent diseases, sometimes life-threatening, drive our innovation in plasma-based therapies and other biopharmaceuticals to enhance quality of life. Grifols is focused on treating conditions across a broad range of therapeutic areas: immunology, hepatology and intensive care, pulmonology, hematology, neurology and infectious diseases. With a workforce of over 24,000 employees in more than 30 countries and regions, we are committed to a sustainable business model that sets the standard for continuous innovation, quality, safety and ethical leadership in the industry. Our work has a positive social and economic impact in the countries where we operate, creating jobs and generating wealth. People are at the heart of what we do, and we strive to create an inclusive, diverse, fair and equal society. Maintaining and promoting a workforce that reflects this reality leads to enhanced professional relationships and helps us to give our best to patients, donors and customers. In 2022, Forbes has recognized Grifols as one of the “Best Employers for Women,” one of “America’s Best Large Employers” and one of the “75 Best Companies to Work for” in Spain. To maintain a positive community and overall respectful communication, please keep our community guidelines in mind. You will find a full version of our guidelines at https://www.grifols.com/en/grifols-social-media-community-guidelines