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.
IQVIA

Clinical Research Coordinator – Part-time

IQVIA

. Supporting the organization and coordination of study operations .

Posted 10/22/2026part-timeMunich • GermanyMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in clinical research coordination, patient care, and medical documentation while ensuring efficient study operations and effective collaboration with study teams. Proficient in maintaining structured processes and supporting administrative tasks in a clinical environment.

Highest-signal resume keywords
Clinical Research CoordinationPatient CareMedical DocumentationOrganizational SkillsGerman Language Proficiency

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

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

Hard Skills
Clinical Research CoordinationMedical DocumentationData CollectionStudy Operations SupportPatient Visit Coordination
Soft Skills
Organizational SkillsCommunication SkillsTeamwork Skills
Certifications & Qualifications
Registered NurseMedical Assistant
Industry Keywords
Clinical ResearchStudy CoordinationStudy DocumentationTrial Site Management

About the role

Key responsibilities & impact
  • Supporting the organization and coordination of study operations
  • Providing care and support to study participants during scheduled study visits
  • Preparing and coordinating patient visits
  • Supporting study-related documentation and data collection
  • Maintaining and updating study documentation
  • Collaborating with investigators and other members of the study team
  • Supporting administrative and organizational tasks related to the clinical study
  • Ensuring a structured and efficient study process at the trial site

Requirements

What you’ll need
  • Completed training in a medical or nursing field, e.g., registered nurse, medical assistant, or a comparable qualification
  • Experience as a Clinical Research Coordinator, Study Nurse, or Study Coordinator
  • Experience in a clinical research environment
  • Strong organizational skills and a careful, structured approach to work
  • Proficiency in medical documentation
  • Excellent communication and teamwork skills
  • Good command of German

Benefits

Comp & perks
  • Part-time position at 20 hours per week
  • Initial assignment duration of 52 weeks