FSP CRA II

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. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Essential Job duties

The below statement are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned Responsible for all aspects of site management as prescribed in the projects plans General on-site monitoring responsibilities Ensure the study staff who will conduct the protocol have received the proper material and instructions to safety enter patients into the study Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements Ensure the integrity of the data submitted on Case Report Forms(CRFs) or other data collection tools by careful source document review Monitor data for missing or implausible data Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy Ensure audit readiness at the site level Travel, including air travel, may be required and is an essential function of the job Prepare accurate and timely trip reports Responsible for all aspects of registry management as prescribed in the project plans Undertake feasibility work when requested Participate in and follow up on Quality Control Visit(QC) when requested Recruitment of potential investigators, preparation of EC submissions, notification to regulatory authorities, translation of study related documentation, organization of meetings and other tasks as instructed by supervisor Might be requested to work in a client facing environment Track and follow up on Serious Adverse Event(SAE) reporting, process production of reports, narratives and follow up of SAE Independently perform CRF review; query generation and resolution against established data review guidelines on For or client data management systems as assigned by management  Assist with training, mentoring and development of new employees, e.g. co-monitoring  Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned  Perform other duties as assigned by management

Experience

Minimum required:

At minimum of 2 years of clinical monitoring experience is a must. 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 skills 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

Education/Qualifications/Certifications and Licenses

Minimum Required:

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate. Thorough knowledge of ICH Guidelines and understanding of local regulatory requirement Thorough knowledge of monitoring procedures Basic understanding of the clinical trial process Valid Driver’s License

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.

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