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    In-Vivo Coordinator - Adme/Dmpk

    O2h
    0-2 years
    Not Disclosed
    Ahmedabad
    10 Nov. 13, 2024
    Job Description
    Job Type: Full Time Remote 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

    Role Title: In-Vivo Study Coordinator
    Role Summary:
    We are seeking an experienced In-Vivo Study Coordinator to plan, coordinate, and oversee research study protocols. The role involves ensuring that study protocols and regulatory requirements are followed, managing data collection efforts, and maintaining financial and recordkeeping systems. The ideal candidate will be proactive, detail-oriented, and skilled at coordinating complex studies in a collaborative environment.

    Key Responsibilities:

    • Plan and coordinate the initiation of research study protocols.
    • Establish and enforce operating policies and procedures, ensuring adherence to study protocols and regulatory requirements.
    • Develop and maintain recordkeeping systems and procedures.
    • Coordinate data collection efforts with multiple collaborating agencies or institutions.
    • Write and edit reports and manuscripts related to study findings.
    • Maintain financial records for in-vivo studies.
    • Ensure availability of necessary supplies, equipment, and documentation as per the study protocol or SOP.
    • Coordinate the preparation of labels, labelling of sample collection tubes, and other reagents.
    • Manage the preparation of shipment packages for dispatching activities.

    Job Requirements:

    • Master's degree in Life Sciences with 1-5 years of experience in in-vivo studies.
    • Excellent communication skills to ensure seamless coordination within the team and with collaborators.
    • Strong time management skills to handle multiple tasks and meet deadlines.
    • Experience in contributing to the planning, scheduling, and execution of in-vivo studies.
    • Ability to maintain key databases and documents essential to the In-Vivo team operations.
    • Proven ability to evaluate workflows and processes for operational efficiency and resource utilization.
    • Strong data analysis and interpretation skills.
    • Self-motivated with the ability to work independently under tight deadlines.
    • High technical knowledge with meticulous attention to detail.
    • Strong rapport-building skills and the ability to engender trust and respect.
    • Ability to work collaboratively in a focused team environment.
    • Exceptional communication and interpersonal skills for effective interaction with stakeholders.
    • Positive attitude, focus, and a winning mentality, aligned with kindness.
    • Enthusiastic, energetic, and creative with a strong desire to contribute to the growth of the organization.
    • Excellent organizational skills and ability to thrive in a fast-paced, vibrant team environment.

    Job Type:

    • Full-time

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