Skip to main content

Mumbai

  • Undergraduate Summer Research Internship at ICTM

    The Institute of Chemical Technology (ICT) Mumbai was established as the Department of Chemical Technology on 1st October, 1933 by the University of Mumbai, through active support of industries and philanthropists. The Institute was most popularly known as UDCT, Mumbai. Research has been an integral part of ICT since its inception and it has created over 500 first generation entrepreneurs. The UDCT grew significantly in stature and was granted autonomy under UGC regulations by the University of Mumbai and further converted in to an Institute on 26th January, 2002. Under the World Bank TEQIP programme, the Maharashtra government granted it full autonomy in June 2004. Due to the recommendations of the Government of Maharashtra and University of Mumbai, the ICT was granted Deemed University Status by the MHRD on 12th September, 2008, with all provisions of the UGC for funding and support as the state owned deemed university.

  • Job as Business Development Executive in VELP Healthcare | 2 Openings - Only Mumbai candidates

    VELP Healthcare communications is a Media and publishing house catering to Healthcare industry & products offered are on Brand communication and promotion in Pharmaceutical companies

    Post: Business Development Executive : Only MUMBAI candidate 2 openings

  • 4th National Level Workshop on Computer Aided Drug Designing at Pune

    RASA Life Science Informatics in collaboration with Padmashree Dr. D. Y. Patil Institute of Pharmaceutical Science and Research

    Is organizing the

     "4th National Level Workshop on Computer Aided Drug Designing”

    7th March to 9th March 2014.

  • Recruitment for B.Pharm/M.Pharm as Research Assistants in Institute of Chemical Technology | Walk in Interview - 13 different projects

    Applications are invited from interested candidates as research assistants for the various research projects for TEQIP-II Centre of Excellence in Process Intensification (CoE-PI) supported by MHRD, GoI New Delhi. The details related to various projects, eligibility criteria are given below:

    Post: Research Assistants

  • Bioinformatics Institute of India invites admissions for career Boosting Distance Learning & E-learning Programs in Pharma & Life sciences for year 2014- 100 % Job Assistance in industry

  • Admissions: Ph.D. in Pharmaceutical Sciences at SVKM’s NMIMS

    Shobhaben Pratapbhai Patel School of Pharmacy & Technology Management (SPPSPTM) was founded in 2006 with a vision to serve the healthcare system of our country. All our courses are reviewed regularly in consultation with our Board of Studies, which comprises people from Pharma Industry, Research, FDA and top academicians from all over India. Thus, the courses are tailor-made to fulfill the requirements of the growing Pharma Industry.

  • Enrolment Closing for the Professional Training Programs in Clinical Research and Pharmacovigilance (via Distance Learning) at Catalyst Clinical Services Pvt. Ltd.

    The enrolment for the Feb’14 batch of Professional Diploma in Clinical Research (PDCR) and Professional Certificate in Pharmacovigilance (PCPV) program is closing on 10-Feb-2014.Please send your Application Form by the due date in order to secure enrolment in Feb’14 batch

    These training programs are aimed at imparting knowledge and skills required for clinical research and pharmacovigilance profession thereby enabling the participants to explore a career in these emerging streams. Optimal course fee and ease of training and evaluation has led to the wider acceptability of the programs amongst students and researchers.

    Program(s) Highlights   Clinical Research and PV Opportunities
    • Optimal Duration : 6 months correspondence program, requires approximately 80 hours of total reading.
    • Assignment based evaluation, no written examination.
    • Optimal Course Fee.
    • Comprise of high quality study modules in line with the requirements of the clinical research and PV Industry.
    • Wide recognition and acceptance of the program through out the industry making PDCR India's largest CR training program.
    • Placement guidance provided to successful participants.
      • Global Clinical Research (CR) industry is estimated at $52 bn ofwhich CRO marketsize is estimated at$17.8 bn.
    • More than 2600 clinical trials are being conducted in India across 5000+investigator sites (ctri.nic.in)
    • The Pharmacovigilance (PV) market worldwide was $1860 million in 2008 & is estimated to reach $2252 million by 2015.
    • India is the fourth largest producer of pharmaceuticals in the world with more than 6,000 licensed drug manufacturers and over 60,000 branded formulations.
    • In India more than 150 companies are actively engaged in Clinical Research and Pharmacovigilance field.

     

    Professional Diploma in Clinical Research (PDCR)
    Module 1: Introduction to Pharmaceutical Medicine
    - New Drug Discovery
    - Clinical Development of Drug
    - Essential Clinical Trial Documents etc.
    Module 2: Good Clinical Practice (GCP) Foundations
    - History of GCP - milestones in the evolution of GCP
    - Principles of GCP
    - Ethics in Clinical Research
    - Biostatistics etc.
    Module 3: Drug Regulatory Affairs (Clinical Trials)
    - Overview of Regulatory Environment in USA, Australia, Europe & India
    - Clinical Trial Application Requirements in India
    - HIPAA Privacy Rule
    - IND/ANDA/New Drug Application etc.
    Module 4: Roles & Responsibilities of Clinical Trial Personnel

    READ MORE >>>

     

    Professional Certificate in Pharmacovigilance (PCPV)
    1. Introduction to Pharmacovigilance (PV) and Risk Management
    2. Standard Terms and Definitions
    3. Global Perspective of PV and ADR Reporting
    4. Guidelines and Standard Governing PV
    5. Global AE Reporting System and Reporting Forms
    - US FDA Form 3500 and 3500A
    - Medicines and Healthcare Products and Regulator Agency's Vigilance Reporting Form-Yellow Card
    - Medeffect Canada and Canada Vigilance Program
    - Suspected Adverse Drug Reaction Reporting (SADRR) Form
    - Universally Accepted ADR Reporting Form CIOMS I Form etc.
    6. Individual Case Safety Reports (ICSRs)
    7. Medical Dictionary for Drug Regulatory Activities (MedDRA)
    8. Periodic Safety Update Reports (PSURs)
    9. Expedited Reporting and Requirements
    10. PV Inspection and Compliance Monitoring

    READ MORE >>>

    Jobs & Opportunities after PDCR & PCPV
    Loading...

    Clinical Research Associate (CRA), Clinical Research Coordinator (CRC), Clinical Data Manager (CDM ), Drug Safety Associate (DSA) etc.

    Highlights of PDCR and PCPV Programs:
    Ease of Training and Evaluation: Distance learning mode and Assignments based evaluation
    Optimal Duration: 6 months
    Course Fee: Rs. 9600 each (DD in favour of Catalyst Clinical Services Pvt. Ltd. payable at Delhi)
    Last Date of Enrolment: 10th February 2014

    Follow the links below to download the Application Form. Our placement assistance can also be viewed on the same link,

    << DOWNLOAD APPLICATION FORM FOR PDCR >>

    << DOWNLOAD APPLICATION FORM FOR PCPV >>

    Enrolment Procedure:
    In order to enrol, one simply needs to send us the duly filled Application Form (available at the links above), copy of highest qualification certificate and DD of prescribed fee to the address mentioned in the footer of the Application Form.

    Advantages of PDCR and PCPV Programs:
    - Increases the visibility of your CV
    - Equip you with the required knowledge to handle the potential interview questions
    - Wide recognition and acceptance of the program(s) throughout the industry
    - Placement assistance via regular job postings on CR Network

    Contact Details:
    Catalyst Clinical Services Pvt. Ltd.
    Corporate office:
    503, NDM-2, Netaji Subhash Place, Pitampura, Delhi – 110034, India
    M:
    +91 9818356273; Ph: +91-11-45121445, 45121435
    Email
    : info@catalystclinicalservices.com

  • Opportunity to work as Area Sales Executive in Reputed client of Aspiring-Solutions specialized in medical devices (sleep therapy & Critical Care)

    Our client is an ISO certified company and broadly caters to three categories – Medical Equipment, Electronic Weighing and Corporate Promotional Products. our client has their own manufacturing facilities at Rabale, Navi Mumbai with in-house R&D, Design and Production.

    Post: Area Sales Executive (Mumbai-Central Line/ Vadodara/ Delhi)

  • Advanced Centre for Treatment, Research and Education in Cancer recruiting Clinical Trial Coordinator | Walk in interview

    The Advanced Centre for Treatment, Research and Education in Cancer (ACTREC, Kharghar, Navi Mumbai is the new state-of-the-art R&D satellite of the Tata Memorial Centre (TMC), which also includes under its umbrella the Tata Memorial Hospital (TMH), the largest cancer hospital in Asia. ACTREC has the mandate to function as a national centre for treatment, research and education in cancer. TMC is an autonomous grant-in-aid institution of the Department of Atomic Energy (DAE), Government of India. It is registered under the Societies Registration Act (1860) and the Bombay Public Trust Act (1950). Its Governing Council is headed by the Chairman, Atomic Energy Commission, Government of India.

    Post: Clinical Trial Coordinator

  • Opening for M.Sc/ M.Pharm/ Ph.D as Senior Research Scientist in Piramal Life Sciences Limited

    Piramal Life Sciences Limited (PLSL) is an independent research-driven drug company that was recently demerged from Piramal Healthcare Limited (Formerly known as Nicholas Piramal India Limited). PLSL was formerly the NCE R&D division of NPIL. PLSL has state-of-the-art R&D laboratories built over 200,000 square-feet of space in Mumbai, India and over 300 scientists engaged in drug discovery and development.

    Post: Senior Research Scientist

Subscribe to Mumbai