Centralized CTL
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Job Location:
Yearly Salary:
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
Fortrea is seeking a proactive and detail-oriented Centralized Clinical Team Lead I to join our Global Clinical Operations this global role you will lead central monitoring and other clinical operation activities across multiple clinical studies ensuring high-quality execution and compliance with industry standards. Youll collaborate with cross-functional teams drive process improvements and play a key part in risk management and study analytics.
Key Responsibilities
- Lead and oversee central monitoring activities for multiple studies ensuring accurate tracking and status reporting.
- Review monitoring visit reports identify risks and communicate trends or safety concerns to study teams.
- Manage protocol deviation review and trend analysis
- Act as quality events owners driving on-time closure
- Act as a liaison between CRAs CTLs and Project Managers for timely issue resolution.
- Support the creation of trip report templates guidelines and study documentation.
- Ensure compliance with Fortrea SOPs ICH Guidelines and GCP
Qualifications
- University/College Degree (Life Science preferred) or certification in an allied health profession.
- 2 years of experience in trip report review and/or centralized/risk-based monitoring.
- 6-8 years of clinical research experience.
- Strong working knowledge of ICH GCP and regulatory requirements.
- Advanced computer skills (MS Office Suite).
- Excellent planning organizational and communication skills.
- Strong interpersonal and leadership abilities.
Learn more about our EEO & Accommodations request here.
