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    Technical Trainer/Subject Matter Expert (Sme)

    Veeda Clinical Research Limited
    4-8 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: Technical Trainer/Subject Matter Expert (SME)

    Company: Veeda Clinical Research Limited
    Location: Ahmedabad, India
    Position: Technical Trainer/Subject Matter Expert (SME)
    Experience: 4-8 Years
    Qualification: M.Sc. / B.Pharm / M.Pharm

    Company Overview

    Veeda Clinical Research Limited is a leading Contract Research Organization (CRO) dedicated to providing comprehensive clinical research and drug development services globally. We specialize in delivering high-quality solutions that adhere to regulatory standards and drive advancements in healthcare.

    Job Summary

    As a Technical Trainer/Subject Matter Expert (SME) at Veeda Clinical Research Limited, you will play a crucial role in developing and delivering training programs to enhance technical knowledge and skills across the organization. You will serve as a mentor and resource for colleagues, ensuring proficiency in clinical research methodologies, regulatory guidelines, and industry best practices.

    Key Responsibilities

    • Training Program Development:

      • Design, develop, and update training materials, modules, and curricula based on organizational needs and industry trends.
      • Customize training programs to address specific technical areas, including clinical trial conduct, regulatory requirements, and scientific methodologies.

    • Training Delivery and Facilitation:

      • Conduct training sessions, workshops, and webinars for employees at various levels to enhance technical competence and compliance with SOPs.
      • Utilize effective instructional techniques and adult learning principles to engage participants and facilitate learning outcomes.

    • Subject Matter Expertise:

      • Serve as a subject matter expert (SME) on clinical research, pharmacology, and related disciplines, providing guidance and expertise to project teams and stakeholders.
      • Stay updated on emerging trends, technologies, and regulatory changes in the clinical research industry to inform training content and delivery.

    • Quality Assurance and Compliance:

      • Ensure training programs align with Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and other relevant regulatory guidelines.
      • Monitor and evaluate training effectiveness through assessments, feedback mechanisms, and performance metrics.

    • Collaboration and Stakeholder Engagement:

      • Collaborate with cross-functional teams, including HR, Quality Assurance, and Operations, to coordinate training initiatives and promote organizational learning.
      • Foster a culture of continuous learning and professional development within the organization.

    • Documentation and Reporting:

      • Maintain accurate records of training activities, participant attendance, and evaluations.
      • Prepare reports and analysis on training outcomes, effectiveness, and areas for improvement.

    Qualifications and Skills

    • Educational Background:

      • Master's degree in Science (M.Sc.) or Bachelor's degree in Pharmacy (B.Pharm / M.Pharm) or related field.

    • Experience:

      • 4-8 years of experience in clinical research, pharmaceutical training, or related roles within the pharmaceutical industry or CRO.

    • Technical Expertise:

      • Profound knowledge of clinical trial processes, drug development lifecycle, and regulatory requirements (ICH-GCP, FDA, EMA, etc.).
      • Demonstrated expertise in developing and delivering technical training programs and materials.

    • Communication Skills:

      • Excellent verbal and written communication skills in English.
      • Ability to effectively communicate complex concepts and information to diverse audiences.

    • Training and Facilitation Skills:

      • Proven experience in conducting training sessions, workshops, or seminars using instructional techniques and interactive learning methods.
      • Strong facilitation skills with the ability to engage participants and create an interactive learning environment.

    • Analytical and Problem-Solving Abilities:

      • Strong analytical skills with attention to detail and ability to analyze training needs and evaluate training effectiveness.
      • Ability to identify issues, propose solutions, and drive continuous improvement in training programs.

    • Teamwork and Leadership:

      • Ability to work independently and collaboratively in a team-oriented environment.
      • Leadership qualities to inspire and mentor colleagues towards achieving organizational goals.

    What We Offer

    • Competitive compensation package based on experience and qualifications.
    • Comprehensive benefits including healthcare coverage, professional development opportunities, and a supportive work environment.
    • Opportunity to contribute to the growth and development of clinical research professionals at a leading CRO.

    How to Apply

    Interested candidates who meet the qualifications are encouraged to submit their resume and cover letter to careers@veedacr.com with the subject line "Application for Technical Trainer/SME - Ahmedabad."

    Join Veeda Clinical Research Limited and make a significant impact by fostering technical excellence and professional development in clinical research through effective training and mentorship.

    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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