As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.
Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.We are seeking an experienced professional to lead central monitoring activities, ensure the quality of clinical trial processes, and proactively manage risk.
As a Centralized Clinical Team Lead, you will play a vital role in ensuring compliance, mentoring teams, and delivering data-driven insights that enhance trial outcomes.Key Responsibilities:Review trip reports, identify risks, and communicate trends to study teams.Execute and oversee central monitoring activities, including study analytics, risk assessment, and mitigation planning.Lead initiatives in trip report optimization and provide mentorship to CRAs and other team members.Develop strategies for risk-based monitoring, including SDV and risk trigger management.Collaborate on regulatory readiness and ensure effective cross-functional team coordination.Qualifications:Degree in Life Sciences or related field; advanced qualifications preferred.8+ years in clinical research, with 2+ years in centralized monitoring or trip report review.Expertise in ICH-GCP guidelines and regulatory compliance.Strong organizational, analytical, and interpersonal skills.Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials.
Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need.
Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.