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Clinical research courses

  • AWARD OF DBT-JUNIOR RESEARCH FELLOWSHIP (DBT-JRF) IN BIOTECHNOLOGY at National Centre for Cell Science

    Applications are invited from Indian nationals for the award of “DBT-Junior Research Fellowship” (DBT-JRF) for pursuing research in frontier areas of Biotechnology and Applied Biology. JRFs will be selected according to merit under two categories: Category I & II. Category I fellowship (Top 275 in number) are tenable in any University/Institute in India where the students can register for Ph.D. Category II students (100 in number) will be eligible to join any DBT sponsored Project and avail fellowship equivalent to NET/GATE qualifications as per DST Guidelines, subject to selection through institutional selection process. Fellowship will be co-terminus with the duration of project and institutional rules will be applicable. There will be no binding on PIs of DBT sponsored projects to select JRF/SRF for their projects from category II list. Selection in Category II will not entitle student for any fellowship from DBT-JRF programme.

    Post: Junior Research Fellowship

  • Opening to work as Medical coding specialist I in Icon Clinical Research

    ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies ICON enjoys a strong reputation for quality and is focused on staff development.
    We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.

    Post: Medical coding specialist I - 008628

  • Required for Drug Safety Associate / Senior Drug Safety Associate in Icon Clinical Research - degree in pharmacy, science

    ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies
    ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.

    Post: Drug Safety Associate / Senior Drug Safety Associate - 008559

  • Vacancies for Business Manager (2 posts) at Renewcell - Nakoda Marketing (Bangalore, Chennai) | Locals preferred

    Nakoda Marketing Pvt. Ltd. was incepted/ incorporated in 1999. With its marketing office at mumbai, nakoda marketing Pvt. Ltd. started its nationwide ethical operations, and within few years of launch, company expanded its specialty range with more than 30 latest products and widened its horizons to mark its presence in the Indian derma/ cosmetology field.

  • 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.

  • 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

  • Opportunity to work as Compliance Specialist in Icon Clinical Research

    ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies
    ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.

    Post: Compliance Specialist - 008156

  • 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
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    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

  • Vacancies for B.Pharm, M.Pharm, M.Sc in Par Formulations in department of Regulatory Affairs, Production, QC, Technical services | Preference for Tamilnadu natives

    Par Formulations Pvt. Ltd. a subsidiary of Par Pharmaceutical Companies Inc. (USA) is an USFDA approved facility located in Chennai facilitating Research & Development and engaged in manufacturing solid 6 semi solid dosage forms. Par Pharmaceutical Inc., is the 5th largest Generic Pharmaceutical Company in the US market and leader in Product Development and In-Licensing of generic pharmaceuticals with state of the art manufacturing facilities. In order to expand the operations of the Research & Development and Manufacturing unit in Chennai, we seek suitable candidates for the following positions:

    Post: General Manager / Dy. General Manager / Manager / Reviewer / Assistant Manager / Team Leader / Analyst / Supervisor / Technician

  • Job for Document Management Associate/Assistant in Icon Clinical Research

    ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies
    ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.

    Post: Document Management Associate/Assistant - 008035

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