Perform other duties as assigned by management
Experience:
Minimum Required:
A minimum of 2 – 3 years of Clinical Monitoring experience is preferred, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job can be substituted.
Ability to monitor study sites independently according to protocol monitoring guidelines, SOP, and local regulatory Guidelines
Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
Good planning, organization, and problem- solving abilities
Ability to work with minimal supervision
Good communication and interpersonal skills
Good analytical and negotiation skills
Computer competency
Fluent in local office language and in English, both written and verbal
Works efficiently and effectively in a matrix environment
Preferred:
1 – 2 years of experience in onsite monitoring for Oncology, Neurology, Ophthalmology, Cardiology and Endocrinology is preferred, however an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
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.
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