Job Description

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. 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 Proactively learn to design and execute processes related to programming, setup, support of clinical and/or safety databases like Medidata Rave or Oracle Inform or SAS programming. Perform the following duties with the guidance from Senior staff: Database design, EDC / SAS edit programming, listings, ad-hoc/scheduled reports using SAS/Cognos/Business Objects - XI, R and other tools for data cleaning and reporting. Complete assigned work utilizing EDC tools or SAS or other proprietary software according to Covance SOPs, Work Instructions, and project specific guidelines in accordance with Good Clinical Practices. Maintain knowledge and awareness of latest developments in CDISC standards and Statistical programming. Create CRF annotations and mapping specifications as per Clients/CDISC standards. Develop and maintain SAS programs for creation of SAS datasets as per the specifications. Develop programs to import external data and transform to SAS Dataset or Excel files for data review and reconciliation. Perform all work with knowledge of regulations pertaining to computerized systems to projects to ensure compliance and interact with project team members in related discipline. Continuously learn and improve communication, technical, and problem-solving skills. Provide regular status update on the tasks assigned to Line Manager. Perform other duties as assigned by Managers and/or Senior Programming staff. 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. For more information about Fortrea, visit www.fortrea.com. 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. For more information about Fortrea, visit www.fortrea.com. 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 information about how we collect and store your personal data, please see our Privacy Statement.

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