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Clinical courses

 

Clinical research courses

  • Learn Clinical Research online| Join India’s leading research institution- Clini Launch Research Institution

    At CliniLaunch, we are dedicatedly providing comprehensive and cutting-edge training and certification programs to healthcare professionals or students seeking a successful career in the pharmaceutical, biotechnology, life sciences, and medical fields. We specialize in Clinical Research, Medical Coding, Clinical SAS, Pharmacovigilance domain, and ensure that pharma graduates should be well-equipped with the knowledge and skills required for their career growth and expansion.

    Course Name
    Clinical Research
    Post Graduate Diploma in Clinical Research
    Advanced Diploma in Clinical Research
    Certification in Clinical Research

    Medical Coding
    Advanced Diploma in Medical Coding
    CPC Training

    Clinical SAS
    Advanced Diploma in Clinical SAS
    Certification in Clinical SAS

    Enquire now >>

    Eligibility Criteria for Clinical Research online and offline course
    Eligibility criteria for bets clinical research training in online and offline mode
    ● Candidates must complete their high school diploma or equivalent qualification.
    ● Candidates must have good command over English and must have command over grammar, punctuation, spelling.
    ● Candidates should be familiar with basic knowledge of computer skills and typing proficiency.
    ● Candidates should understand medical terms, physiology, and anatomy.
    ● Candidates must have keen eye on details, able to work independently, accurately and efficiently in the fast paced environment.
    ● No age limit for the right candidate for clinical research training course.

    Click here to Enquire >>

    Why Clini Launch Research Institute
    ● Live online training with virtual classroom
    ● CLRI sets 5000+ aspirants in rumored MNCs for CDM, SAS, PV and others.
    ● Learning management system access with video, e-book, presentation and podcast.
    ● A SAS accredited clinical research institute
    ● ISO 9001: 2015 Clinical Research institute
    ● Direct placement support
    ● Tie up with multiple organizations in India to accomplish 1005 placement situation records.

    How to Join
    Click on the link and share your details with us. We will help you with the program details and registration process.

    Click here to enroll>>

    Placements
    CliniLaunch has witnessed selection of 20% students in IQVIA, 15% students in Accenture, 25% students in Omega Healthcare, 10% in AugMedix, 20% in NYX RCM Pvt. Ltd., and 10% in Fortrea

    For more details click the link below : ENQUIRE NOW>>

    Visit Website- www.clinilaunchresearch.in

  • Sanofi looking for Regulatory Affairs Manager
    The Regulatory Manager is a scientific leadership role that leads the regulatory activities involved in the India, Srilanka, Nepal, Maldives market. The role provides the regulatory strategies, and regulatory submissions of new products for various brands in Rx, OTC, Food supplements in support of the new and existing portfolio
  • ADVANZ PHARMA looking for Regulatory Affairs Executive
    Assessing Change request assigned to ensure regulatory assessment along with strategy and documents required for any regulatory submissions are shared with stakeholder in a timely fashion.
  • Job for Pharma and Life Sciences Candidates at Tata Memorial Centre

    The Tata Memorial Centre is a Comprehensive Cancer Centre with a mission to achieve the highest standards in patient care, cancer prevention, cancer research and professional development for oncology and allied disciplines. TMC is an autonomous body funded, controlled by the Department of Atomic Energy, Government of India. TMC is affiliated to Homi Bhabha National Institute.

    Required for the post of Clinical Trial Co-ordinator on DAE-CTC Project (A/c No. 963) (Initially for a period of six months.) 

  • Ferring Pharmaceuticals looking for Senior Manager Contract Manufacturing & Development
    Skills for handling various soft tools for procurement and inventory management of all raw materials, packing materials and finished products.
  •  

    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/Professional Diploma

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

    PROFESSIONAL CERTIFICATION

    Good Clinical Practice (GCP) Professional
    Clinical Research Associate
    Pharmacovigilance Associate (PV Associate)
    Drug Safety Aggregate Reporting
    MedDRA Coding
    Pharmacovigilance Audits & Inspections

     

    ENQUIRE NOW >>

    ✓ Programme duration: 12 months for Post Graduate Diploma and 6 months for Professional Diploma and Professional Certification programmes.

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

       ✓ Placement Assistance

    ENQUIRE NOW >>

  • Job for M.Pharm, MSc as Medical Writing Associate at Teva
    M.Sc or M.Pharm. Coordinate with all concerned department to ensure timelines and compliance to regulatory or sponsor requirements for preparation, compilation and delivery of reports. Electronically generate, review study documents and submission of study reports in CTD/eCTD format as per regulatory requirements.
  • Work as Business Development Senior Manager at Sun Pharma
    The incumbent would need to build a strong New Product Portfolio and its management and delivery in a time bound manner for India Business of Sun. Works closely with the Business/Marketing, Business Development, R&D, Manufacturing, Regulatory, IP, Market Research, SFE, CEO Office, Commercial, Medical, Clinical Research, CQA, Finance, PMO, New Product Launch, Network Strategy, Packaging development teams etc.
  • Novo Nordisk looking for CDC Trial Manager - B.Pharm, BSc Apply
    As a CDC Trial Manager is the main accountable person in making sure that deliverables are met as per project timelines, within budget and complying with Protocol, country regulatory requirements, Helsinki Declaration, GCP, Good Clinical Practice, and NN SOPs Standard Operating Procedures. bachelor degree in life science, pharmacy, or nursing qualification or equivalent.
  • Abbott looking for Vaccine Associate - M.Pharm, B.Pharm, MSc Apply
    Successfully launch assigned brands in a specialty segment in line with brand strategy. Plan and consistently achieve patients on therapy, unit targets and value targets. B.Pharm / M.Pharm / M.Sc. candidates preferred.
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