Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Novo Nordisk

Student Assistant

Novo Nordisk

. Support CRAs with activities related to trial start-up, conduct and close-out .

Posted 9/22/2026part-timeCopenhagen • DenmarkEntry Level💰 DKK 209 per hourWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates strong organizational and detail-oriented skills in supporting clinical trial activities, including documentation management and coordination of trial supplies. Proficient in communication in both Danish and English, with a focus on collaboration across cross-functional teams.

Highest-signal resume keywords
Clinical Trial CoordinationDocumentation ManagementStrong Communication SkillsDigital Tools ProficiencyOrganizational Skills

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Soft Skills
Detail-OrientedStructured Work ApproachIndependent WorkCollaboration
Industry Keywords
Clinical DevelopmentTrial Start-UpTrial Close-OutQuality ComplianceClinical ResearchAdministrative SupportLife SciencesHealthcare

About the role

Key responsibilities & impact
  • Support CRAs with activities related to trial start-up, conduct and close-out
  • Prepare, quality-check, maintain and archive trial documentation and site materials in line with quality and compliance requirements
  • Coordinate, track and ship clinical trial equipment, patient materials and study supplies to clinical sites
  • Support reporting, meeting preparation, documentation and follow-up across trial teams
  • Assist with administrative processes such as purchase orders and payments
  • Contribute to selected ad hoc projects and continuous improvements across CDC DK
  • Work closely with Clinical Research Associates, Trial Managers, Clinical Trial Assistants and other cross-functional colleagues
  • Report to the Clinical Operations Manager, CDC DK

Requirements

What you’ll need
  • Current enrolment in a Bachelor's programme within life sciences, healthcare or a related field
  • Structured, organised and detail-oriented way of working
  • Confidence working with digital tools and systems
  • Strong written and verbal communication skills in Danish and English
  • Genuine interest in clinical development, coordination and administrative support
  • Ability to work independently while collaborating effectively with colleagues across functions, teams and countries
  • Ideally at least two years of studies remaining (useful, but not essential)

Benefits

Comp & perks
  • Pension scheme with 10% employer contribution and 5% employee contribution
  • Approximately 15 hours per week
  • High degree of flexibility to plan working hours around studies and other commitments
  • Additional flexibility during exam periods whenever possible
  • Opportunity to work from home depending on the nature of tasks and business needs
  • Hands-on experience and opportunities to grow skills through collaboration across teams and countries