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.

Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Responsibilities include, but are not limited to:1.

Trial and site administration: Track (e.g.

essential documents) and report Ensure collation and distribution of study tools and documents2.

Document management: Prepare documents and correspondence Collate, distribute/ship, and archive clinical documents, e.g.

e TMFAssist with e TMF reconciliation Execute e TMF Quality Control Plan3.

Site Start-Up responsibilities: Collaborate with other country roles to: In a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start-up and submissions Obtain, track and update study insurance certificates4.

Budgeting, Agreement and Payments: Collaborate with finance/budgeting representatives for: Develop, control, update and close-out country and site budgets (including Split site budget)Develop, negotiate, approve and maintain contracts (e.g.

CTRAs)Track and report contract negotiations Update and maintain contract templates (in cooperation with Legal Department)Calculate and execute payments (to investigators, vendors, grants)Ensure adherence to financial and compliance procedures Monitor and track adherence and disclosures Maintain tracking tools5.

S/AE Claim Management: Support Financial Clinical Operation Manager(F-COM) for: Coordinate meetings Update and maintain tracking tools Develop and maintain settle agreements Coordinate for payments Collate, distribute/ship, and archive relevant documents Qualifications, Skills& Experience CORE Competency Expectations: Fluent in Local Languages and business proficient in English (verbal and written) and excellent communication skills Good understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines.

Hands on knowledge of Good Documentation Practices Good IT skills (Use of MS office, use of some clinical IT applications on computer) and ability to adapt to new IT applications.

Strong MS Excel skills required.

ICH-GCP Knowledge appropriate to role Excellent negotiation skills for CTCs in finance area Behavioral Competency Expectations: Effective time management, organizational and interpersonal skills, conflict management Effective communication with external customers (e.g.

sites and investigators)High sense of accountability / urgency.

Ability to set priorities and handle multiple tasks simultaneously in a changing environment Works effectively in a matrix multicultural environment.

Ability to establish and maintain culturally sensitive working relationships.

Demonstrates commitment to Customer focus, both internally and externally.

Able to work independently Proactive attitude to solving problems / proposing solutions Experience Requirements: Minimum 1 - 2 years in Clinical Research or relevant healthcare experience Educational Requirements: Completed job training (office management, administration, finance, health care preferred) or B.

A./B. S.

(Life Science preferred) or equivalent healthcare experience.

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.