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    Sr Clinical Trials Administrator (Ctc)

    Fortrea
    1+ years
    Not Disclosed
    Remote
    10 Sept. 5, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    About Fortrea

    Fortrea, a leading global Contract Research Organization (CRO), excels in scientific rigor and clinical development expertise. We offer a comprehensive range of clinical development, patient access, and technology solutions across over 20 therapeutic areas. With more than 19,000 employees in over 90 countries, Fortrea is at the forefront of transforming drug and device development to benefit partners and patients worldwide.

    Position: Clinical Trial Administrative Associate

    Are you seeking a stable position with a reputable company? Do you value working in a supportive and friendly environment? Join us in accelerating the delivery of groundbreaking therapies and tackling future drug development challenges. At Fortrea, you'll be part of a team dedicated to building new possibilities for our clients.

    Key Responsibilities:

    • Site-Specific Materials: Prepare study site-specific materials in compliance with relevant SOPs.
    • Documentation Management: Set up and maintain clinical investigator files and documentation.
    • Data Entry: Enter and maintain data in selected study tracking databases.
    • Document Preparation: Prepare study-related documents and materials for archiving at appropriate intervals.
    • Payment Support: Assist with payment activities, including preparing invoices, reconciliation, and creating purchase orders.
    • Administrative Duties: Perform other administrative tasks as assigned.

    Education and Qualifications:

    • Degree: Bachelor's degree in Life Sciences.
    • Experience: Minimum of 1 year of clinical trial-related administrative experience (e.g., Clinical Trial Associate, Clinical Research Coordinator, Study Coordinator).
    • Knowledge: Basic understanding of Good Clinical Practice (GCP), ICH Guidelines, and local regulations.
    • Skills: Exceptional administrative skills, experience in managing multiple priorities, and meeting deadlines.
    • Interpersonal Skills: Strong oral and written communication skills, good social and time management skills.
    • Technical Proficiency: General computer literacy, particularly in Excel.
    • Work Environment: Ability to work effectively in a matrix environment and independently.

    Additional Information:

    • This role requires working 4 days per week from the client office.

    Join Us:

    Fortrea is actively seeking motivated problem-solvers and innovative thinkers who are passionate about advancing clinical trials. We are committed to revolutionizing drug development and improving patient outcomes. Join our team to thrive in a collaborative workspace where your professional growth is supported and your contributions make a global impact. For more information, visit www.fortrea.com.

    Equal Opportunity Employer:

    Fortrea is an Equal Opportunity Employer committed to fostering diversity and inclusion. We do not tolerate harassment or discrimination and make employment decisions based on individual qualifications and business needs. We encourage all qualified candidates to apply.

    For information on how we handle your personal data, please refer to our Privacy Statement.

    Contact:

    Thomas Leader
    Email: thomas.leader@covance.com

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