IQVIA Biotech
Clinical Research Associate 2(m/w/x)
Full-timeRemoteExperienced
Frankfurt am Main, München, Hamburg
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PSPSI CRO
Clinical Research Associate / Senior Clinical Research Associate(m/w/x)
München
Full-timeWith Home OfficeSenior
Nejo AI Summary
Onsite and remote monitoring of AMG Phase II/III studies, including CRF review and source document verification. Independent on-site monitoring experience in Germany required. Flexible working conditions, structured onboarding.
Requirements
- College/University degree in Life Sciences or equivalent education/training/experience
- Independent on-site monitoring experience in Germany; Switzerland experience is a plus
- Independent monitoring visit experience in AMG studies, Phases II/III
- Oncology, Hematology, Infectious/Rare/Gastro-intestinal Diseases experience is a plus
- Full professional proficiency in German and English; French/Italian skills are an asset
- Advanced proficiency in MS Office applications
- Ability to plan, multitask, and work in dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel and valid driver’s license
Tasks
- Conduct onsite and remote monitoring visits
- Perform CRF review and source document verification
- Resolve queries during monitoring visits
- Manage site communication and relationships
- Participate in site identification process
- Train less experienced CRAs
- Lead assigned studies with true ownership
- Work across multiple sponsors and therapeutic areas
- Focus on fewer protocols for deeper study engagement
- Build strong site relationships nationwide
- Work on complex and scientifically interesting trials
- Operate with responsibility and autonomy
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- German – Native
- English – Native
- French – Basic
- Italian – Basic
Tools & Technologies
- MS Office
Benefits
Mentorship & Coaching
- Structured onboarding
- Continuous mentoring
Modern Equipment
- Technologically integrated environment
Flexible Working
- Flexible working conditions
- Work-life balance
Informal Culture
- Trust, visibility, and recognition
Career Advancement
- Career development opportunities
- Internal growth paths
Job Security
- Stable environment
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of PSI CRO and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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PSPSI CRO
Clinical Research Associate / Senior Clinical Research Associate(m/w/x)
München
Full-timeWith Home OfficeSenior
Nejo AI Summary
Onsite and remote monitoring of AMG Phase II/III studies, including CRF review and source document verification. Independent on-site monitoring experience in Germany required. Flexible working conditions, structured onboarding.
Requirements
- College/University degree in Life Sciences or equivalent education/training/experience
- Independent on-site monitoring experience in Germany; Switzerland experience is a plus
- Independent monitoring visit experience in AMG studies, Phases II/III
- Oncology, Hematology, Infectious/Rare/Gastro-intestinal Diseases experience is a plus
- Full professional proficiency in German and English; French/Italian skills are an asset
- Advanced proficiency in MS Office applications
- Ability to plan, multitask, and work in dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel and valid driver’s license
Tasks
- Conduct onsite and remote monitoring visits
- Perform CRF review and source document verification
- Resolve queries during monitoring visits
- Manage site communication and relationships
- Participate in site identification process
- Train less experienced CRAs
- Lead assigned studies with true ownership
- Work across multiple sponsors and therapeutic areas
- Focus on fewer protocols for deeper study engagement
- Build strong site relationships nationwide
- Work on complex and scientifically interesting trials
- Operate with responsibility and autonomy
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degree
Languages
- German – Native
- English – Native
- French – Basic
- Italian – Basic
Tools & Technologies
- MS Office
Benefits
Mentorship & Coaching
- Structured onboarding
- Continuous mentoring
Modern Equipment
- Technologically integrated environment
Flexible Working
- Flexible working conditions
- Work-life balance
Informal Culture
- Trust, visibility, and recognition
Career Advancement
- Career development opportunities
- Internal growth paths
Job Security
- Stable environment
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of PSI CRO and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
PSI CRO
Industry
Pharmaceuticals
Description
The company is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation.
Not a perfect match?
- IQVIA Biotech
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