Clinical Research Associate CRA
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Job Location:
Monthly Salary:
Posted on:
12 hours ago
Vacancies:
1 Vacancy
Job Summary
Clinical Research Associate (CRA) Drive Impact in Global Clinical Trials
At Fortrea we are redefining whats possible in clinical research. As a global CRO built on innovation integrity and scientific excellence we empower our teams to make a meaningful impact on the future of healthcare. Here youll grow your career work with purpose and join a community that values flexibility continuous learning and bold thinking.
About the Role
As a Clinical Research Associate you will play a critical role in protecting study participants ensuring highquality clinical data and supporting the successful execution of global trials. Youll partner closely with investigative sites and crossfunctional teams serving as the face of Fortrea throughout the study lifecycle.
Key responsibilities include:
- Conducting all site monitoring activities (PreStudy Initiation Monitoring and Closeout) in compliance with Fortrea SOPs ICHGCP protocols and regulatory requirements.
- Ensuring subject safety through informed consent verification and protocol adherence.
- Safeguarding data integrity via source data verification source document review and query management.
- Maintaining complete and current regulatory documentation and ensuring site audit readiness.
- Managing IP accountability site supplies and investigational material storage.
- Acting as Lead CRA on assigned studies when required.
- Preparing monitoring plans trip reports training content and site initiation materials.
- Supporting SAE tracking documentation review and eClinical system upkeep.
- Collaborating closely with study teams to ensure critical timelines and deliverables are met.
- Assisting with onboarding and training of new CRAs through comonitoring and knowledge sharing.
Qualifications What Were Looking For
Essential Qualifications
- University degree or certification in a related health or science field or equivalent experience.
- Minimum 2 years of clinical monitoring experience (internal or external).
- Strong understanding of ICH GCP monitoring procedures and regulatory requirements.
- Ability to independently conduct site monitoring per SOPs and monitoring plans.
- Strong communication skills in English and local language.
- Excellent planning problemsolving and organizational abilities.
- Experience with SAE processes and eClinical systems (e.g. CTMS).
Preferred Qualifications
- Experience with Fortrea SOPs and systems.
- Additional experience in medical clinical pharmaceutical research or datarelated fields.
- Phase I monitoring experience.
- Life Sciences or Nursing background.
- Strong attention to detail and methodical approach to work.
- Understanding of physiology pharmacology or medical device requirements.
- Strong interpersonal negotiation and customerfocused mindset.
Why Join Fortrea
Because here your work matters. When you join our global community youll experience:
- Purposedriven work contribute to studies that advance patient care worldwide.
- Continuous learning benefit from training programs mentoring and career mobility.
- Flexibility and balance collaborate in a peoplecentered environment that supports you.
- Innovation at scale work with cuttingedge technology across diverse therapeutic areas.
- Opportunities to grow explore advancement pathways across clinical operations and beyond.
Ready to make an impact
If youre passionate about advancing science and driving highquality clinical research wed love to meet you. Apply today and build your career with a global leader in clinical development.
Fortrea is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
Key Skills
- CSS
- Cloud Computing
- Health Education
- Actuary
- Building Electrician
