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Clinical Intern

  • Internship
    Full-time
    Summer Internship
  • Research & Development
    Healthcare
  • Waltham
    Remote

AI generated summary

  • You should be pursuing a life sciences degree, 18+, reliable, eager to learn about drug development, self-motivated, organized, have good interpersonal skills, and moderate MS Office skills.
  • You will assist with clinical trial tasks, prepare study documents, manage the Trial Master File, maintain trackers, monitor vendor systems, and support special projects as needed.

Requirements

  • Pursuing a bachelor’s or master’s degree in the life sciences or related fields
  • Minimum of 18 years old
  • Reliable and punctual with an ability to adhere to a general work schedule both in person and remotely
  • Desire to learn about the drug development process in a biotechnology setting
  • Self-motivated, organized, and capable of working as a member of a team
  • Good interpersonal skills
  • Moderate skill using Microsoft Office
  • Good communication skills (written and verbal) with attention to detail

Responsibilities

  • Perform various clinical trial tasks as delegated by the Clinical Operations Team
  • Follow internal filing plan to reconcile files from previous studies
  • Assist with the preparation of study-related documents, tools, and templates (e.g. site newsletters, internal team updates slides)
  • Provide support and participate in clinical trial systems oversight and review
  • Contribute to timely and quality Trial Master File (TMF) management and completeness
  • Maintain internal trackers and monitor various vendor systems to provide metrics and administrative support as needed
  • Assisting with special projects and/or tasks as required.

FAQs

What is the duration of the internship?

The internship is for 8-12 weeks.

Is this internship paid?

Yes, this is a paid internship.

What will the intern be working on?

The intern will work closely with the Clinical Operations team to become familiar with clinical trial execution and drug development, completing various clinical trial tasks as delegated.

What educational background is required for this position?

The candidate should be pursuing a bachelor’s or master’s degree in the life sciences or related fields.

Are there any age requirements for this internship?

Yes, candidates must be a minimum of 18 years old.

Will the intern need to attend meetings?

Yes, the intern will attend weekly project team meetings to learn about the early stage lifecycle of biologic drug development.

What skills are preferred for this role?

Candidates should have moderate skill using Microsoft Office, good interpersonal skills, and strong written and verbal communication skills with attention to detail.

Is there any travel required for this position?

No, there is no travel required for this internship.

What type of tasks will the intern perform?

The intern will assist with clinical trial tasks, preparation of study-related documents, maintain internal trackers, and contribute to Trial Master File management.

What qualities are desired in an intern for this role?

The ideal candidate should be highly motivated, self-organized, and capable of working effectively as part of a team.

Consulting
Industry
11-50
Employees
2008
Founded Year

Mission & Purpose

Cedent provides an agile and optimized business process enabling you to concentrate on executing your strategy and be sure that your IT systems and processes back your initiatives. We offer consultancy services that range from IT strategy and process consulting to technology consulting and solution architecture.