(CCS-011) SITE READINESS AND REG SPECIALIST I

Recommended: - university/college degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology) and 2 years work experience in clinical research, including a strong working knowledge of the ich guidelines and fda, irb/iec regulations. minimum required: minimum 2 years of experience in clinical development or regulatory process. working knowledge of ich, fda, irb/iec, and other applicable regulations/guidelines; familiarity with investigator start-up documents and contract/budgets negotiation process; previous interaction with operational project teams and investigative sites - demonstrated understanding of research protocol requirements and proven ability to communicate with/educate others about them fortrea is proud to be an equal opportunity employer: as an eoe/aa employer, fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. we make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. we encourage all to apply. for more inform...