Be the connection between science and solutions. As a Clinical Research Associate I or II (CRA I / CRA II) you will take your first or next step into clinical research supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is well suited for earlycareer professionals including candidates coming from internships or with up to 1 year of onsite monitoring experience who are eager to learn and grow in a structured supportive environment.
You will contribute to the execution of clinical studies across a variety of therapeutic areas including Oncology Dermatology Respiratory Cardiology and Diabetes gaining broad exposure and handson experience while developing your monitoring skills.
This role is for upcoming future opportunities that may arise at Fortrea.
Key Responsibilities:
Support the management of clinical trial sites in compliance with Fortrea SOPs ICHGCP study protocols and sponsor requirements with appropriate supervision.
Assist in the preparation and conduct of site monitoring activities including site initiation routine monitoring and closeout visits ensuring patient safety and protocol adherence.
Perform source data verification (SDV) support query resolution and review eCRFs to help ensure data quality and completeness.
Maintain and update essential trial documentation in eTMF and sponsor systems to support inspection readiness.
Support investigational product (IP) tracking and accountability checks in collaboration with the study team.
Collaborate with crossfunctional teams and escalate issues appropriately contributing to site performance quality and timelines.
Required Qualifications :
University or college degree in life sciences nursing pharmacy or a related field; relevant internships or equivalent experience will be considered.
Entrylevel to 1 year of experience in clinical research including internships trainee roles or up to 12 months of onsite monitoring experience.
Basic understanding of ICHGCP guidelines and clinical trial processes.
Strong attention to detail willingness to learn and ability to follow established procedures and documentation standards.
Fluency in German and English both written and spoken.
Comfortable using clinical systems and tools with openness to travel as required for site visits.
Why Join Us
Grow your clinical research career in a structured and supportive environment with clear development pathways and mentoring.
Gain handson exposure to global clinical trials and multiple therapeutic areas while building strong foundational CRA skills.
Benefit from formal training programs modern clinical systems and continuous learning opportunities.
Enjoy a flexible work model competitive benefits and a culture that values collaboration quality and wellbeing.
We welcome applications from earlycareer candidates who are motivated to build a career in clinical research and grow with Fortrea. If you are curious detailoriented and eager to make an impact on patients lives we encourage you to apply.
#LI-GQ1 #LI-Remote
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
Be the connection between science and solutions. As a Clinical Research Associate I or II (CRA I / CRA II) you will take your first or next step into clinical research supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is well suited for ear...
Be the connection between science and solutions. As a Clinical Research Associate I or II (CRA I / CRA II) you will take your first or next step into clinical research supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is well suited for earlycareer professionals including candidates coming from internships or with up to 1 year of onsite monitoring experience who are eager to learn and grow in a structured supportive environment.
You will contribute to the execution of clinical studies across a variety of therapeutic areas including Oncology Dermatology Respiratory Cardiology and Diabetes gaining broad exposure and handson experience while developing your monitoring skills.
This role is for upcoming future opportunities that may arise at Fortrea.
Key Responsibilities:
Support the management of clinical trial sites in compliance with Fortrea SOPs ICHGCP study protocols and sponsor requirements with appropriate supervision.
Assist in the preparation and conduct of site monitoring activities including site initiation routine monitoring and closeout visits ensuring patient safety and protocol adherence.
Perform source data verification (SDV) support query resolution and review eCRFs to help ensure data quality and completeness.
Maintain and update essential trial documentation in eTMF and sponsor systems to support inspection readiness.
Support investigational product (IP) tracking and accountability checks in collaboration with the study team.
Collaborate with crossfunctional teams and escalate issues appropriately contributing to site performance quality and timelines.
Required Qualifications :
University or college degree in life sciences nursing pharmacy or a related field; relevant internships or equivalent experience will be considered.
Entrylevel to 1 year of experience in clinical research including internships trainee roles or up to 12 months of onsite monitoring experience.
Basic understanding of ICHGCP guidelines and clinical trial processes.
Strong attention to detail willingness to learn and ability to follow established procedures and documentation standards.
Fluency in German and English both written and spoken.
Comfortable using clinical systems and tools with openness to travel as required for site visits.
Why Join Us
Grow your clinical research career in a structured and supportive environment with clear development pathways and mentoring.
Gain handson exposure to global clinical trials and multiple therapeutic areas while building strong foundational CRA skills.
Benefit from formal training programs modern clinical systems and continuous learning opportunities.
Enjoy a flexible work model competitive benefits and a culture that values collaboration quality and wellbeing.
We welcome applications from earlycareer candidates who are motivated to build a career in clinical research and grow with Fortrea. If you are curious detailoriented and eager to make an impact on patients lives we encourage you to apply.
#LI-GQ1 #LI-Remote
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
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