Iqvia
Healthcare
ClinicalResearchAssociate1or2(m/w/d)
“Clinical Research Associate 1 or 2 (m/w/d) at Iqvia. Skills: Site selection, Site initiation, Site monitoring, Site close-out, Subject recruitment, Regulatory requirements, Good Clinical Practice, ICH guidelines, Case report form, Data query resolution, Remote-monitoring, Study start-up, Therapeutic area specialization. Perform site selection visits. Perform site initiation visits”
Industry & Context.
Flexibility to travel 40-60%, Driver’s license class B
What They're Looking For.
Must Have
12 month of on-site monitoring experience, Knowledge of GCP and ICH guidelines, Fluency in German (C1 level), Good command of English, Driver’s license class B
Nice to Have
University Degree in life science, University Degree in scientific discipline, Apprenticeship in health care field
What You'll Do.
Perform site selection visits
Perform site initiation visits
Perform site monitoring visits
Perform site close-out visits
Support development of recruitment plan
Evaluate site practice quality
Evaluate site practice integrity
Manage regulatory submissions progress
Manage recruitment progress
Manage CRF completion progress
Manage data query resolution progress
Collaborate with study site experts
Collaborate with client representatives
Perform remote-monitoring
Involve in study start-up processes
Specialize on therapeutic area
Mentor less experienced team members
Support as subject matter expert
How You'll Work.
Team & Collaboration
Study site experts; Client representatives; Less experienced team members
Communication Scope
Written communication; Verbal communication
Applying for this Clinical Research Associate 1 or 2 (m/w/d) role?
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