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Biotechnology

 

Clinical courses

 

Clinical research courses

  • Recruitment for Life sciences candidates at NICPR

    Hands on Training in HPV- DNA Diagnostics DHR funded. Preference will be given to the candidates who have qualified the any national exam such as GATE/Net (JRF/LS) or any other equivalent exam.
  • Job for M.Pharm, M.Tech, M.S Pharm as SRF at IIT-BHU
    Senior Research Fellow to work on CCRAS-sponsored Evaluation of Coded drug Ayush Rasayana B for treatment of high-altitude sickness using multi-dimensional drug discovery approach project.
  • Opportunity for M.Pharm, MSc as Research Fellow at Institute of Life Sciences

    Institute of Life Sciences (ILS), Bhubaneswar, an autonomous institute of the Department of Biotechnology, Ministry of Science & Technology, Government of India invites applications from the Indian Nationals to join the following position sanctioned under ICMR-funded project.

    Post : Research Fellow (01 position)

  • CSMCRI invites applications for Research Internship
    Marine products: Seaweed valorization, seaweed polysaccharides, bioplastics, marine-based natural products synthesis, marine bioactives, antimicrobial/biocidal activities; algenic acid to sugar alcohol conversion.
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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 >>

  • Multiple Job openings at Centre for Cellular and Molecular Biology
    Molecular breeding in rice / Marker-Assisted Selection in rice, Phenotyping of yield, biotic and abiotic stress traits, rice field management, Plant Molecular Biology/Plant-Microbe Interactions using rice plant as a model system 
  • Work as Quality Control Associate / Senior Associate at Stelis Biopharma
    Preparation of quality system related, Instrument operation related SOPs, Specification, STPs, GTPs, raw data sheet, certificate of analysis. Preparation, review, execution of method transfer and method validation protocols and reports etc.
  • Opportunity for M.Pharm or MTech to work in ICMR-DHR sponsored project at ICT, Mumbai
    Evaluation of immunomodulatory and anti-cancer properties of Hydroxychavicol, a major constituent of Piper betel. Perform the project related experiments, develop new techniques and protocols for drug screening using cell culture technology.
  • Work as Research Intern at National Institute of Immunology
    The research intern will perform cloning, and over expression of proteins along with bioinformatic analysis. The preference will be given to candidates who have background knowledge in at least two of the following areas: Molecular Biology, Protein biochemistry, Structural Biology, and Bioinformatics
  • Require Regulatory Professional at Novo Nordisk
    As Regulatory Professional II, the candidate will be responsible for making the timely submissions to the Health Authorities worldwide. The candidate is expected to establish and maintain the CMC part of the core regulatory file. 
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