SSU CTA

Fortrea
paid time off, flex time, 401(k)
United States, North Carolina, Durham
Sep 14, 2024
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. We are seeking aSite Start-up, Clinical Trial Assistant Specialist who will be responsible for providing support for day to day site start up activities under general supervision of the Site Start Up Manager(s).The position will also support existing departmental tasks and may take on developmental tasks as appropriate upon discussions with manager. Responsibilities: Assists the Site Start Up team to deliver the clinical trial start up activities within agreed timelines. Assists in authoring/contributing to clinical trial start up documents and trial related plans developed by CROs and vendors. Assists the SSU team with reporting, meeting minutes, presentation slides, and document tracking and filing. Manages the documenting of study related issues and escalations, and communicates as appropriate with SSU Manager/SB&C Manager Maintains knowledge and acts as team super user or subject matter expert for related systems and processes. Maintains up to date training record attending internal/external training(s) as necessary. Participates in inter-departmental workgroups to create or enhance processes. Requirements: Education Bachelor's Degree required. Experience 1 year experience in similar/relevant field (eg.Sponsor, CRO, Clincal trial Vendor, Clincal Coordinator, etc.) Proficiency with Microsoft Teams, Word, Excel, PowerPoint, Outlook, and SharePoint. Ability to work with minimal supervision and complete tasks according to deadlines Ability to take ownership and manage tasks as well as communicate effectively Ability to collaborate with others to drive deliverables forward Must be able to work in a fast paced environment Demonstrate ability to prioritize multiple competing tasks Fluent business English (oral and written) Benefits: All job offers will bebased on a candidate's skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), Paid time off (PTO) or Flexible time off (FTO). #LI - Remote Application deadline isSeptember 6th, 2024. 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 ourPrivacy Statement.