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    Project Coordinator

    Veeda Clinical Research Limited
    2-4 years
    Not Disclosed
    Ahmedabad
    12 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: Project Coordinator

    Company: Veeda Clinical Research Limited
    Location: Ahmedabad, India
    Position: Project Coordinator
    Experience: 2-4 Years
    Qualification: B.Pharm

    About Veeda Clinical Research Limited

    Veeda Clinical Research Limited is a premier global clinical research organization based in Ahmedabad, India. We provide comprehensive clinical research services to the pharmaceutical, biotechnology, and medical device industries. Our commitment to scientific excellence, regulatory compliance, and ethical standards is reflected in our dedication to conducting high-quality clinical trials.

    Job Summary

    As a Project Coordinator at Veeda Clinical Research Limited, you will play a pivotal role in managing and coordinating clinical research projects. You will ensure that projects are completed on time, within budget, and in compliance with regulatory requirements and company standards. Your role will involve close collaboration with various stakeholders to support the successful execution of clinical trials.

    Key Responsibilities

    • Project Planning and Coordination:

      • Assist in the development of project plans, including timelines, budgets, and resource allocation.
      • Coordinate and track project activities to ensure they are on schedule and within scope.

    • Stakeholder Communication:

      • Serve as a primary point of contact for project-related communication with internal teams, clinical sites, sponsors, and regulatory bodies.
      • Facilitate effective communication and collaboration among all project stakeholders.

    • Documentation and Reporting:

      • Maintain comprehensive project documentation, including study protocols, informed consent forms, and regulatory submissions.
      • Prepare and distribute regular project status reports and updates to stakeholders.

    • Quality Assurance and Compliance:

      • Ensure that all project activities adhere to Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and regulatory requirements.
      • Assist in the preparation for and conduct of internal and external audits and inspections.

    • Risk Management:

      • Identify potential project risks and develop mitigation strategies.
      • Monitor and manage project issues and changes to ensure minimal impact on project timelines and outcomes.

    • Resource Management:

      • Coordinate with project teams to ensure adequate resource allocation and utilization.
      • Assist in the management of project budgets and financial tracking.

    • Training and Support:

      • Provide training and support to project team members on project-specific processes and requirements.
      • Assist in the onboarding of new project staff and ensure they are informed about project protocols and procedures.

    Qualifications and Skills

    • Educational Background:

      • Bachelor’s degree in Pharmacy (B.Pharm).

    • Experience:

      • 2-4 years of experience in clinical research or project management, preferably within the pharmaceutical or clinical research industry.

    • Technical Skills:

      • Understanding of clinical trial processes, GCP, and regulatory requirements.
      • Proficiency in using project management software and tools (e.g., MS Project, Trello, Asana).

    • Organizational Skills:

      • Excellent organizational and time-management skills.
      • Ability to manage multiple tasks and prioritize effectively in a fast-paced environment.

    • Communication Skills:

      • Strong written and verbal communication skills.
      • Ability to effectively interact with a diverse group of stakeholders, including researchers, clinical staff, sponsors, and regulatory authorities.

    • Analytical Skills:

      • Strong analytical and problem-solving skills.
      • Ability to identify issues, analyze data, and develop solutions.

    • Interpersonal Skills:

      • Excellent interpersonal skills and ability to work effectively as part of a team.
      • Ability to foster a positive and collaborative working environment.

    What We Offer

    • Competitive salary and benefits package.
    • Opportunities for professional growth and development.
    • A supportive and collaborative work environment.
    • The chance to contribute to innovative clinical research and improve patient outcomes.

    How to Apply

    Interested candidates are invited to submit their resume and a cover letter detailing their relevant experience and qualifications to careers@veedacr.com with the subject line "Application for Project Coordinator."

    Join Veeda Clinical Research Limited and contribute to advancing medical science and improving patient outcomes through high-quality clinical research and project management.

    Note: This job description is intended to provide a general overview of the position and may include other responsibilities and qualifications as required by Veeda Clinical Research Limited.

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