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  • 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

  • Candidates with B.Pharm/M.Pharm invited to attend WALK-IN-INTERVIEW for Technical Assistant in National Institute of Nutrition
    Candidates with B.Pharm/M.Pharm invited to attend WALK-IN-INTERVIEW for Technical Assistant in National Institute of Nutrition

    National Institute of Nutrition (NIN) was founded by Sir Robert McCarrison in the year 1918 as ‘Beri-Beri’ Enquiry Unit in a single room laboratory at the Pasteur Institute, Coonoor, Tamil Nadu. Within a short span of seven years, this unit blossomed into a "Deficiency Disease Enquiry" and later in 1928, emerged as full-fledged "Nutrition Research Laboratories" (NRL) with Dr. McCarrison as its first Director. It was shifted to Hyderabad in 1958.

    Eligible candidates are invited to attend a WALK-IN-INTERVIEW on the following date sharp at 09:30 a.m. for the following position on the ad hoc research project entitled “Assessment of Safety of Second Hand Glass Bottle by the pharma, food and liquor Industries in Country – a Pilot Study” funded by ICMR at this Institute. The essential qualification, experience, consolidated Pay and the tenure of the post is as under: The late comers will not be allowed in any circumstance for attending the written test/Interview.

    Post: Technical Assistant 1 No. (OBC)

  • Walk in for Research Associate in ICAR
    Walk in for Research Associate in ICAR

    The Indian Council of Agricultural Research (ICAR) is an autonomous organisation under the Department of Agricultural Research and Education (DARE), Ministry of Agriculture, Government of India. Formerly known as Imperial Council of Agricultural Research, it was established on 16 July 1929 as a registered society under the Societies Registration Act, 1860 in pursuance of the report of the Royal Commission on Agriculture. The ICAR has its headquarters at New Delhi.

    Applications are invited for the posts of one Research Associate (RA) of a project under the National Fund for Basic, Strategic and, Frontier Application Research in Agriculture (NFBSFARA) at Central Institute of Post-Harvest Engineering and Technology, Ludhiana, Punjab. The appointments will be purely temporary under contractual and co-terminus basis, following the prescribed procedure for six months or till the completion date of the project. The appointments may be terminated at any time without notice or assigning any reason thereof.

    Post: Research Associate

  • 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
    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

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

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

  • CSIR-IICT is conducting Walk-in-lnterview for the position of Project Assistant - 8 posts
    CSIR-IICT is conducting Walk-in-lnterview for the position of Project Assistant - 8 posts

    Indian Institute of Chemical Technology (IICT), Hyderabad, a constituent of CSIR is a leading research Institute in the area of chemical sciences. The core strength of IICT lies in Organic Chemistry, and it continues to excel in this field for over six decades. The research efforts during these years have resulted in the development of several innovative processes for a variety of products necessary for human welfare such as drugs, agrochemicals, food, organic intermediates, adhesives etc. More than 150 technologies developed by IICT are now in commercial production.

    CSIR-IICT is conducting Walk-in-lnterview for the following positions on a purely temporary basis for the sponsored projects at 10.00 A M on 10th February 2014 at IICT Hyderabad:

    Post: Project Assistant

  • Career for M.Sc./ B.Pharma as Executive/Jr. Executive – IPQA, QA (Oncology) in Panacea Biotec
    Career for M.Sc./ B.Pharma as Executive/Jr. Executive – IPQA, QA (Oncology) in Panacea Biotec

    Panacea Biotec is a leading research based Health Management Company, with an annual turnover of approx. Rs. 830 Crores. We are engaged in research, development, manufacture & marketing of Vaccines, Bio-Pharmaceuticals and Pharmaceuticals (Rx & OTC) of international quality and Health Services. All Panacea Biotec plants are accredited by international agencies and they follow current Good Manufacturing Practices, as per WHO guidelines.
    We offer stimulating work environment & a career that spells growth. In tune with our plans, we require young, aggressive, dynamic, high performing and result oriented professional.

    Post: Executive/Jr. Executive – IPQA, QA (Oncology)

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

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