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    Clinical Research Coordinator

    The Start Center For Cancer Research
    2+ years
    Not Disclosed
    Remote, USA
    10 July 18, 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, 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

    Job Opportunity: Clinical Research Coordinator

    Company: START Center for Cancer Research
    Location: Remote, with operations in the United States, Spain, Portugal, and Ireland
    Contract: Full-time, Permanent

    Company Overview:

    START Center for Cancer Research specializes in Phase 1 clinical trials for innovative anti-cancer therapies, providing patients access to advanced treatment options globally. With a strong presence in community oncology centers, START has conducted over 1,300 early-phase clinical trials, contributing to FDA/EMA approvals for 43 therapies.

    Best-in-Class Benefits and Perks:

    • Comprehensive Health Coverage: Medical, dental, and vision insurance provided.
    • Robust Retirement Planning: 401(k) plan with employer matching.
    • Financial Security: Life and disability insurance coverage.
    • Flexible Financial Options: Health savings and flexible spending accounts.
    • Well-being and Work-Life Balance: Paid time off, flexible scheduling, and remote work options.
    • Professional Development: Collaborative environment fostering growth and learning.

    Role Overview: Clinical Research Coordinator

    As a Clinical Research Coordinator at START Center for Cancer Research, you will manage multiple clinical trial protocols, ensuring compliance with regulatory requirements and ethical standards. Your role involves coordinating patient participation, maintaining study documentation, and facilitating communication between stakeholders.

    Responsibilities:

    • Protocol Management: Oversee assigned studies, ensuring adherence to protocol requirements, SOPs, and Good Clinical Practice.
    • Communication: Maintain professional correspondence with study sponsors, CROs, CRAs, and internal staff regarding protocol updates and issues.
    • Patient Coordination: Assist in patient screening, eligibility assessment, and informed consent processes, ensuring compliance and patient understanding.
    • Documentation: Manage study documentation, including source documents and protocol deviations.
    • Training and Implementation: Implement study protocols and amendments, train staff on protocol procedures, and ensure adherence throughout the study.

    Qualifications:

    • Education: Bachelor’s degree required.
    • Experience: Minimum 2 years in patient care or clinical research, preferably in oncology.
    • Certification: CCRP or CCRC credentials preferred, demonstrating clinical research knowledge.
    • Skills: Proficiency in healthcare equipment and understanding of ethical considerations in human subjects research.

    About START Center for Cancer Research:

    Founded in Texas in 2007, START Center for Cancer Research operates globally with a focus on accelerating cancer treatment advancements. With state-of-the-art facilities and a multidisciplinary approach, START offers comprehensive treatment plans and access to cutting-edge clinical research options. The organization is committed to translating research into effective treatments, providing hope to patients and families worldwide.

    Join Our Team:

    If you are passionate about advancing cancer research and improving patient outcomes, join START Center for Cancer Research. Your dedication and expertise can make a meaningful impact in the fight against cancer.

    Equal Opportunity Employer:

    START Center for Cancer Research values diversity and is an equal opportunity employer. We celebrate and embrace differences in our workforce, fostering an inclusive environment where everyone can contribute to our mission without discrimination based on race, color, religion, age, disability, genetic information, gender identity, or any other protected status under applicable law.

    Become part of a team dedicated to revolutionizing cancer treatment through groundbreaking research and patient-centered care. Apply now to help us conquer cancer, one clinical trial at a time.

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