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  • Walk in for Project Fellow, Project Assistant in Indian Institute of Toxicology Research - 4 posts

    Eligible and interested candidates may attend the interview for purely temporary engagement as Project Fellow, Project Assistant Level-I & Level-II under different externally funded Project tenable at Indian Institute of Toxicology Research, Lucknow. Project wise vacancy position, Date of Interview and qualification details are as under

    Post: Project Fellow, Project Assistant

  • Career opportunity as Area Sales Executive - Delhi @ reputed client of Aspiring Solutions

    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-Delhi (1 Nos., Male Candidates Only)

  • Vacancies for Area Sales Executive - Vadodara | Aspiring-Solutions hiring for its reputed client specialized in medical devices

    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-Vadodara (2 Nos., Male Candidates)

  • 5th National Seminar on BIOINFORMATICS, 2014 in SVIMS Bioinformatics Centre

    We extend our cordial invitation to attend DBT sponsored 5th National seminar on BIOINFORMATICS to be organized by SVIMS Bioinformatics Centre, SVIMS University, Tirupati from 14-15th February 2014. The main objective of the National conference is to bring together scientists, researchers, students from academia and corporate companies to share their informatics research experiences in the field of molecular modeling and drug design. Moreover, the participants will get opportunities to enlighten their bioinformatics skills to implement in their respective research field. Researchers will also be encouraged to present their research works.

  • Indian Drugs & Pharmaceuticals Ltd. require B.Pharm, M.Pharm, M.Sc for department of production, QC, QA, purchase | 7 posts

    IDPL is the largest Central Pharma Public Sector Undertaking in India with plants at Rishikesh, Gurgaon & Hyderabad and two Subsidiary Units at Chennai and Muzaffarpur. IDPL played a major role in the strategic National Health Programmes like Family Welfare Programme & Population Control (Mala-D & Mala-N) anti-malarials (Chloroquine) and prevention of dehydration (ORS) by providing quality medicines. During the country’s calamity of outbreak of Plague in 1994, IDPL was the only company which played the sheet anchor role in supplying Tetracycline for the entire Nation. Similarly, company had made uninterrupted supply of Chloroquine to combat Malaria epidemic in different parts of the country.

    Post: Dy.G.M, Divisional Manager, Manager/Dy. Manager (QC), Executive (Purchase), Stores Executive, Production Executive

  • 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

  • Career for Manager/Senior Manager/Associate Director Regulatory CMC in Novartis

    A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

    Post: Manager/Senior Manager/Associate Director Regulatory CMC

  • Walk in as Officer - Pharmacovigilance at Wipro BPO | B.Pharm / B.Sc (Nursing) / M.Sc (Nursing)

    Wipro Infotech is the leading strategic IT partner for companies across India and Middle East - offering integrated IT solutions. We plan, deploy, sustain and maintain your IT lifecycle through our total outsourcing, consulting services, business solutions and professional services. Wipro Infotech helps you drive momentum in your organisation - no matter what domain you are in.

  • Vacancy for post of Medical Representative at Nakoda Marketing | Fresher

  • 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

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