Clinical Research Associate II / Senior Clinical Research (CRA) (m/w/x) Germany

Consulting, Inc.; Ulm; On-site; EUR 65,000 - 85,000; Full time

Job summary

CTI is seeking a Clinical Research Associate II / Senior CRA for Germany (m/w/x). The role involves monitoring responsibilities across sites in Ulm, with remote work options.

You will manage site visits, regulatory documentation, and study start-up activities, collaborating with project teams to advance clinical programs. Ideal candidates have 3–5 years of CRA experience in Germany, a life science degree, and strong ICH-GCP knowledge, along with fluent German and English.

Qualifications

• 3–5 years clinical research experience as a CRA or related profession in Germany
• Life science background
• Excellent knowledge of ICH-GCP and regulatory requirements
• Fluent German and English (B2)

Responsibilities

• Serve as main CTI contact for assigned study sites
• Conduct site visits (PSV, SIV, IMV, COV) and deliverables within monitoring plan timelines
• Assist with study start-up activities including feasibility and site selection
• Collect, review and track essential/regulatory documents
• Participate in training and meetings; may include presentations
• Create and implement subject enrollment strategies for sites
• Ensure proper storage and accountability of Investigational Product and materials
• Perform site management updates to Clinical Project Manager
• Conduct remote monitoring per Monitoring Plan
• Use systems and reports to track subject status, CRF retrieval, SDV, regulatory docs, and IP
• Assist with project-specific activities as a Project Team member

Skills

CRA experience

Independent monitoring

Fluent German & English

German language proficiency (B2+)

Education

Life science degree

Job description

Clinical Research Associate II / Senior Clinical Research (CRA) (m/w/x) Germany

Job Category: Clinical Monitoring

Requisition Number: CLINI001933

• Posted : July 17, 2026
• Full-Time
• Remote

Locations

Showing 1 location

Germany - Ulm
Ulm, Germany
Schillerstrasse 1/15
Ulm, 89077, DEU

Germany - Ulm
Ulm, Germany
Schillerstrasse 1/15
Ulm, 89077, DEU

• Serve as main CTI contact for assigned study sites
• Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP
• Assist with or oversee study start-up activities, including feasibility, pre-study activities and site selection
• Collect, review and track essential/regulatory documents
• Participate in and complete all general and study specific training as required
• Participate in investigator, client and project team meetings; may include presentations
• Create and implement subject enrollment strategies for assigned study sites
• Ensure proper storage, dispensation and accountability of all Investigational Product (IP) and trial-related materials
• Perform site management activities and provide ongoing updates of site status to Clinical Project Manager
• Conduct remote monitoring and complete related activities in accordance with study specific Monitoring Plan
• Utilize systems and reports to track subject status, subject case report form (CRF) retrieval / source document review (SDV), regulatory documents, and IP
• Assist with project-specific activities as member of Project Team

WhatYou'llBring:

• 3 - 5 yearsclinical research experience as a CRA or related professionin Germany incl. independent monitoring experience in Germany
• Life science background
• Excellent knowledge in ICH-GCP and regulatory requirement
• Fluent (at least Level B2) in spoken and written language German and English

AboutCTI

• AdvanceYourCareer–Weinvestinyourprofessionalgrowth.Ourstructuredmentoringprogram,leadershipdevelopmentcourses,anddedicatedtrainingdepartmentprovidethesupportyouneedtoexcel.Wealsoencourageongoingeducationtohelpyouachieveyourprofessionalgoals.
• JoinanAward-WinningTeam–Joinaglobalteamspanning60countries,recognizedforitsaward-winningculturethatprioritizespeople.Wesupportyourwork-lifebalancewithhybridworkopportunities.ThroughourCTICaresprogram,you’llhaveopportunitiestogivebacktoyourcommunityandtheworld.
• MakeaLastingImpact–AtCTI,yourworkdirectlycontributestoadvancingmedicine.You’llplayavitalroleindevelopinglife-changingtreatmentsforpatientswithchronicandcriticalillnesses.Together,wemovemedicineforward,makingadifferenceforthosewhoneeditmost.

PleaseNote

• WewillnevercommunicatewithyouviaMicrosoftTeamsortextmessage
• Wewillneveraskforyourbankaccountinformationatanypointduringtherecruitmentprocess