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Clinical courses

  • https://www.cliniindia.com

    LEARN CLINICAL RESEARCH ONLINE LIVE LECTURES WITH LMS ACCESS
    ISO 9001: 2015 | SAS Accredited Institute
    Technology-driven Research and Innovative (TRIP) Pedagogy


    At the Clini India, we are dedicated to providing comprehensive and cutting-edge training programs to individuals seeking a successful career in the pharmaceutical, life science, and medical fields. Our institute specializes in Clinical Research, Clinical Data Management, Pharmacovigilance, and Medical Writing domains, ensuring that our graduates are well-equipped with the knowledge and skills needed to work in these dynamic industries.

     

    Program Offered- Advance Program in Clinical Research & Management (APCRM)

     

    Duration: 4 Months
    Mode: Live Lectures along with LMS Access
    Pre-Recruitment Training with Placement Support

     

    Modules Covered

    • Clinical Trial Operations
    • Clinical Data Management
    • Pharmacovigilance
    • Medical Writing
    • Soft Skills/ Communication Skills Classes

     

    WHO CAN JOIN
    B.Pharm/ M.Pharm/ Pharm.D
    B.Sc/ M.Sc/ Phd Life Sciences/ Chemistry
    MBBS/ BDS/ BAMS/ BHMS etc.
    BPT/ MPT etc.

    Click Here to learn More ▸

     

    WHY CLINI INDIA

    LIVE Online Training with Virtual Classroom

    • A SAS Accredited Clinical Research Institute
    • ISO 9001: 2015 Clinical Research Institute
    • Learning Management System Access (LMS) (24X7) - With Video, Presentations, e-books and Podcasts.
    • Placement Support- with direct team access.
    • India's most trusted clinical research training institute for Industry oriented training.

     

    Career Opportunities:

    Upon completion of our training programs, graduates can explore a wide range of career opportunities, including:

    • Clinical Research Coordinator (CRC)
    • Clinical Research Associate (CRA)
    • Clinical Data Manager
    • Pharmacovigilance Specialist
    • Medical Writer
    • Regulatory Affairs Associate
    • Clinical Project Manager
    • Drug Safety Associate
    • Quality Assurance Specialist

    HOW TO JOIN
    Click on the below link below and send your details, we will help you with the Program details and registration process.
     
    Click to Learn More ▸

     
    PLACEMENTS INFO
    In the last batch, the Institute has witnessed participation of many Life Science students and professionals now working with Fortune 500 and global CRO, Pharma and IT Companies like IQVIA, Covance, Parexel, Indegene, Novartis, Pfizer, Novo Nordisk, Accenture, TCS, Cognizant and many more.
     
    Advanced program in Clinical Research & Management is designed specifically to meet career consolidation goals of Pharma, Life Science, and Medical Graduates. For more details

    Click to Learn More ▸

     

    Visit website- www.cliniindia.com

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    IGIMS was established on 19th November 1983, as an autonomous organisation on the pattern of All India Institute of Medical Sciences, New Delhi. The objective was to provide super specialty medical facilities in Bihar. On 27th January 1983 Cabinet approved the completion of this massive project in 4 phases within a span of six (6) years. According to the decision of State Government, 130.20 Acres of land was transferred to IGIMS.

    Post : Junior Research Fellow (JRF)

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    इंस्टिट्यूट ऑफ़ गुड मैन्युफैक्चरिंग प्रैक्टिसेज इंडिया
    Institute of Good Manufacturing Practices India

    Faculty of Clinical Research and Drug Safety (FCRDS)
    ए- 14/बी, कुतुब इंस्टिट्यूशनल एरिया, ओल्ड जे एन यु कैंपस के समीप, नई दिल्ली - 110067
                        A-14/B, A Block, Qutab Institutional Area, Near Old JNU Campus New Delhi-110067
                         E-mail: info@igmpi.ac.in, Phone: +91 11-26512850, +91 8448963304 (Mobile)
    Website: www.igmpi.ac.in

     

    ENQUIRE NOW >>

    Post Graduate/Executive Diploma

    Clinical Research
    Medical Writing
    Pharmacovigilance
    Clinical Data Management (CDM)
    QA/QC (Clinical Research as Major)
    Pharmacology
    Clinical Engineering and Management

    CERTIFICATE

    Good Clinical Practice (GCP) Professional
    Clinical Research Associate
    Pharmacovigilance Associate (PV Associate)

    PROFESSIONAL CERTIFICATION

    Good Clinical Practice
    Drug Safety Aggregate Reporting
    MedDRA Coding
    Pharmacovigilance Audits & Inspections

     

    ENQUIRE NOW >>

    ✓ Programme duration: 12 months for Post Graduate Diploma and 3-6 months for Certificate programmes.

       ✓ Contact for Prospectus and last date on: +91 11-26512850 or info@igmpi.ac.in

       ✓ Placement Assistance

    ENQUIRE NOW >>

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    Post : Senior Research Fellow (SRF)

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