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    Clinical Research Associate - Oncology - Arizona

    Lifelancer
    2-3 years
    Not Disclosed
    Carolina Beach Remote, USA
    10 Nov. 27, 2024
    Job Description
    Job Type: Full Time Remote Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science/BS/RN 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

    Clinical Research Associate (Oncology) - Arizona

    Join ICON, a leading global clinical research organization powered by healthcare intelligence.

    We are currently seeking a Clinical Research Associate (CRA) with experience in Oncology to join our team. As a CRA, you will play a key role in monitoring and managing clinical trials, ensuring quality care for patients, and providing leadership within the clinical team.

    What You’ll Be Doing:

    • Work on multiple Oncology trials, with a focus on quality of life.
    • Provide regional travel support and mentor junior flex team members.
    • Lead study teams, training other Study Managers (SMs) and developing site startup documents, including Site Initiation Visit (SIV) agenda.
    • Represent LTMs (Lead Trial Managers) or SMs in meetings and review study documents such as Monitoring Guidelines.
    • Support country budget development and contract negotiations with CCS colleagues.
    • Drive patient recruitment strategies at assigned sites and manage site relationships to meet study timelines.

    Primary Responsibilities:

    • Manage multiple clinical trial sites.
    • Mentor and coach junior staff.
    • Review and provide feedback on clinical documents.
    • Support metrics and KPIs as outlined in the Quality Oversight Plan (QOP).
    • Represent key stakeholders and collaborate with internal teams (e.g., Local Trial Manager, Central Study Team, Site Managers).

    What You Need to Have:

    • A minimum of a B.S. degree, R.N., or equivalent, preferably in Biological Sciences.
    • 2-3 years of experience in monitoring pharmaceutical industry clinical trials.
    • 1-3 years of experience in Oncology trials.
    • Knowledge of therapeutic areas and strong analytical/risk-based monitoring skills.
    • Ability to work with various systems and databases (e.g., CTMS, EDC, eTMF, IWRS).
    • Strong communication and influencing skills to manage study sites.
    • In-depth knowledge of Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements.
    • Ability to travel up to 50%.

    Additional Requirements:

    • Must be located in Arizona near a major airport.
    • Legal authorization to work in the U.S. without requiring sponsorship.

    What ICON Offers You:

    • Competitive salary and comprehensive benefits package.
    • A range of health insurance options, retirement planning, and employee assistance programs.
    • Flexible benefits such as childcare vouchers, gym memberships, and health assessments.
    • A diverse, inclusive work environment where innovation thrives.

    At ICON, we embrace diversity and are committed to creating an inclusive workplace free from discrimination.

    Interested? Apply via Lifelancer for this role and other similar opportunities:
    Apply on Lifelancer

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