Iqvia
Life sciences
TraineeClinicalResearchAssociate(m/w/d)
“Trainee Clinical Research Associate (m/w/d) at Iqvia. Skills: Clinical research, Site management. Perform site selection visits. Perform site initiation visits”
Industry & Context.
Problem-solving skills
Regular business travel up to 40-60%
What They're Looking For.
Must Have
Completed advanced training in clinical research, Fluent German (C1 level), Good command of English, Driving license class B, Availability to start on 16. July or 1. August 2026
Nice to Have
Home-office location in North-Rhin-Westphalia, Hesse, Rhineland-Palatinate, Lower Saxony
What You'll Do.
Perform site selection visits
Perform site initiation visits
Perform site monitoring visits
Perform site close-out visits
Maintain appropriate documentation
Support development of subject recruitment plan
Establish regular communication lines
Administer protocol training to sites
Administer study training to sites
Evaluate quality of site practices
Evaluate integrity of site practices
Escalate quality issues
Manage progress by tracking regulatory submissions
Manage progress by tracking recruitment
Manage progress by tracking CRF completion
Manage progress by tracking data query resolution
How You'll Work.
Communication Scope
Written communication; Verbal communication
Applying for this Trainee Clinical Research Associate (m/w/d) role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about Iqvia?
Real rants from real employees. Read before you apply.