Research associate Jobs in München
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Research associate • munchen
Clinical Research Associate
TFS HealthScienceMunich, Bavaria, .DE- Gesponsert
Research Analyst
Warner Bros. DiscoveryMunich, Bavaria, GermanyNetwork Research Engineer
Huawei Research Center Germany & AustriaMünchen, Bayern, DE- Gesponsert
Working Student AI Research
BrainlabMunich, Bavaria, Germany- Gesponsert
Research Associate Assays, Biophysics & Screening (gn)
Proteros BiostructuresPlanegg, Bavaria, Germany- Gesponsert
Research Coordinator
CAALA JobsMünchen, Bavaria, GermanyOnline Data Research - German - Remote
TELUS Digital, MünchenClinical Research Associate
Alexion PharmaceuticalsGermany,Munich- Gesponsert
Jr. Fellow- Research
European Institute of Policy Research and Human Rights SIAMunich, Bavaria, GermanyUser Research Working Student
KICKBASEMunich, Bavaria, GermanyContent Creator : Schwerpunkt Research Reports
Julian HospMunich, Bavaria, Germany- Gesponsert
Research Associate Computational Biologist (all genders)
EvotecMunich, Bavaria, GermanyEntry Clinical Research Associate (Munich Office) - Clinical Trials Experience Required
MEDPACEMunich, Germany- Gesponsert
Praktikant Economics and Research (all genders)
Roland BergerMunich, Bavaria, GermanyResearch Analyst (m / w / d)
TREUGAST Solutions GroupMunich, Bavaria, Germany- Gesponsert
Senior Research Engineer, Data Engine
IntrinsicMunich, Bavaria, GermanyResearch Associate (PhD or Postdoc position) at Lunar & Planetary Exploration
Technical University of MunichMunich, DE- Gesponsert
Research & Development Project Manager
FUTRUE GmbHGräfelfing, deClinical Research Associate
TFS HealthScienceMunich, Bavaria, .DE- Quick Apply
TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.
Join Our Team as a Clinical Research Associate.
About this role
As part of our FSP team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. This role is dedicated to one of our clients.
This role is a full-time role based Germany.
Key Responsibilities :
Monitor clinical trial sites to ensure protocol, GCP, and regulatory compliance
Conduct site visits (initiation, monitoring, and close-out) and prepare visit reports
Verify source data and ensure accurate, timely data entry
Support site staff with study procedures and documentation
Identify, escalate, and help resolve study issues and risks
Qualifications :
Bachelor’s degree in life sciences or a related field
5+ years of CRA or clinical research monitoring experience
Strong knowledge of ICH-GCP and regulatory requirements
Excellent communication, organizational, and time-management skills
Ability to travel as required and work independently
Experience working with women's health studies is a plus
What We Offer
We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients
A Bit More About Us
Our journey began 30 years ago in Sweden, in the city of Lund. As a global CRO with the ultimate goal of ensuring patients’ safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific and the Middle East.
Our core values of Trust, Quality, Flexibility and Passion are what make TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization.
#Together we make a difference