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    Lead-Remote Monitoring

    Veeda Clinical Research Limited
    4-6 years
    Not Disclosed
    Ahmedabad
    10 June 25, 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 Description: Lead - Remote Monitoring

    Company: Veeda Clinical Research Limited
    Location: Ahmedabad, India
    Position: Lead - Remote Monitoring
    Experience: 5-8 Years
    Qualification: B.Pharm / M.Pharm / M.Sc

    Company Overview

    Veeda Clinical Research Limited is a prominent Contract Research Organization (CRO) dedicated to advancing clinical research and drug development. We specialize in providing comprehensive services across the pharmaceutical and biotechnology sectors, ensuring high standards of quality and compliance in every project we undertake.

    Job Summary

    As the Lead - Remote Monitoring at Veeda Clinical Research Limited, you will oversee and manage remote monitoring activities across clinical trials. You will play a crucial role in ensuring the integrity and quality of clinical trial data through effective oversight and adherence to regulatory guidelines and company standards.

    Key Responsibilities

    • Remote Monitoring Oversight:

      • Lead and manage remote monitoring activities for assigned clinical trials, ensuring compliance with study protocols, SOPs, and regulatory requirements.
      • Conduct remote reviews of clinical trial data to identify trends, issues, and risks impacting data quality and study conduct.

    • Team Management and Leadership:

      • Provide leadership and guidance to a team of remote monitoring professionals, ensuring clear communication, effective collaboration, and adherence to timelines and quality standards.
      • Mentor and train team members on remote monitoring practices, regulatory guidelines, and best practices.

    • Quality Assurance and Compliance:

      • Ensure all remote monitoring activities adhere to ICH-GCP guidelines, applicable regulations, and company procedures.
      • Conduct quality checks on remote monitoring reports and documentation to maintain data integrity and accuracy.

    • Risk Management and Issue Resolution:

      • Identify risks and potential issues related to remote monitoring activities and develop mitigation strategies.
      • Escalate significant issues to senior management and collaborate on corrective actions as needed.

    • Stakeholder Engagement:

      • Collaborate closely with clinical operations teams, project managers, and study sponsors to align on remote monitoring strategies and objectives.
      • Provide regular updates and reports on remote monitoring activities, data trends, and study progress.

    • Process Improvement and Innovation:

      • Continuously evaluate and enhance remote monitoring processes, tools, and workflows to optimize efficiency and quality.
      • Champion the implementation of innovative technologies and methodologies to improve remote monitoring practices.

    • Training and Development:

      • Coordinate and conduct training sessions for internal teams and external stakeholders on remote monitoring practices and compliance requirements.

    Qualifications and Skills

    • Educational Background:

      • Bachelor's or Master's degree in Pharmacy (B.Pharm / M.Pharm) or Life Sciences (M.Sc).

    • Experience:

      • 5-8 years of experience in clinical research, with significant experience in remote monitoring activities within the pharmaceutical or CRO industry.
      • Proven track record of leadership and management in clinical trials and remote monitoring projects.

    • Technical Skills:

      • In-depth knowledge of clinical trial operations, remote monitoring methodologies, and data management practices.
      • Strong understanding of ICH-GCP guidelines, regulatory requirements, and industry standards.

    • Leadership and Communication:

      • Excellent leadership skills with the ability to motivate and manage a team effectively.
      • Outstanding interpersonal and communication skills, with the ability to interact confidently with stakeholders at all levels.

    • Problem-Solving Abilities:

      • Strategic thinker with strong analytical skills and the ability to identify and resolve complex issues.
      • Proven ability to implement process improvements and drive innovation in remote monitoring practices.

    • Organizational Skills:

      • Exceptional organizational and time management skills, with a keen attention to detail and the ability to prioritize effectively in a dynamic environment.

    What We Offer

    • Competitive compensation package commensurate with experience and qualifications.
    • Comprehensive benefits including healthcare coverage and opportunities for professional development.
    • A collaborative and inclusive work environment focused on scientific excellence and innovation.

    How to Apply

    Interested candidates who meet the qualifications are invited to send their resume and cover letter to careers@veedacr.com with the subject line "Application for Lead - Remote Monitoring - Ahmedabad."

    Join Veeda Clinical Research Limited and lead the way in advancing clinical research through effective remote monitoring and quality-driven practices.

    Note: This job description provides an overview and may include additional responsibilities and qualifications as required by Veeda Clinical Research Limited.

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