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  • Require Process Associate\ Developer Medical Billing in Genpact

    Genpact Limited, a global leader in business process and technology management services, leverages the power of smarter processes, smarter analytics and smarter technology to help its clients drive intelligence across the enterprise. Genpact’s Smart Enterprise Processes (SEP) framework, its unique science of process combined with deep domain expertise in multiple industry verticals, leads to superior business outcomes. Genpact’s Smart Decision Services deliver valuable business insights to its clients through targeted analytics, reengineering expertise, and advanced risk management. Making technology more intelligent by embedding it with process and data insights, Genpact also offers a wide range of technology services. Driven by a passion for process innovation and operational excellence built on its Lean and Six Sigma DNA and the legacy of serving GE for more than 14 years, the company’s 60,500+ professionals around the globe deliver services to its more than 600 clients from a network of 74 delivery centers across 20 countries supporting more than 30 languages.

    Post: Process Associate\ Developer Medical Billing

  • Job as Senior Clinical Coder in INC Research

    INC Research is a company headquartered in the United States and that the personal information collected on its websites may be sent to, stored or processed in the United States or to any other country in which INC Research or its affiliates, subsidiaries or agents maintain facilities. While INC Research is committed to providing your voluntarily disclosed employment application information with a reasonable level of privacy protection, you should know that the general level of protection for personal information in the United States may not be the same as that provided in other countries. By using the INC Research website and/or providing INC Research with personal identifiable information, you fully understand and unambiguously consent to the transfer and the collection and processing of such information in the United States.

    Post: Sr Clinical Coder (India)

  • Global Institute of Regulatory Affairs provides Industry Oriented Courses in Regulatory Affairs (RA), Quality Assurance & Quality Control (QA/QC) for Life Science Graduates with Placement Assisstance in Pharma Sector

    Global Institute of Regulatory Affairs provides Industry Oriented Courses in Regulatory Affairs (RA), Quality Assurance & Quality Control (QA/QC) for Life Science Graduates with 100% Placement Assistance in Pharma Sector**
    Global Institute of Regulatory Affairs (GIRA) is a change that will help you begin & grow your career in Pharma Industry. GIRA through its industrial expertise offers quality educational programs in the field of Regulatory Affairs and QA/QC. It offers Full time, Part time and Distance Learning courses; this flexibility ensures prior commitments are taken care of and at the same time skills are added to their CVs.

    Certifications: GIRA is an ISO Certified Institute as per the norms of ISO 9001:2008. It is accredited by Joint Accreditation System of Australia & New Zealand (JAS-ANZ).

    Course name: Certificate Course in e-CTD submission(4 months)

    COURSE HIGHLIGHT2 days Hands-on Experience on the e-CTD Software (LORENZ DOCUBRIDGE)

    2 days Hands-on Experience:

    1st Day- A Demo/Step by Step procedure to the Software by the e-CTD expert through a Webinar

    2nd Day- Remote access of the software given to the Applicant to practice the e-CTD submission skills

    “Special 7 days Online Program- Available only for Working Professionals"

    WHO WILL BENEFIT:
    • RA Executives responsible for CTD/DMF Compilation & Submission
    • QC/QA Managers and Staff
    • Documentation department
    • Regulatory Consultants
    • Pharma Freshers looking for Direct Entry in QA/RA Departments

    Program Highlights:
    * Completely Online (From Admission to Examination)
    * Industry Accepted Course Curriculum & Certificate
    * Experienced and Quality Faculty
    * Online Examination (Exams from Home)
    * Online Interaction (Discussion Forums, GIRA Blog)
    * 100 % Placement Assistance & Career Guidance

    Candidates Pursuing Courses from GIRA are associated with:
    Emcure Pharmaceutical Ltd, Novartis Pharma, Dr Reddys Laboratories Ltd, Wockhardt Pharma, Cipla, Glenmark Pharmaceuticals, Himalaya Company, USV Limited, Mylan Labs, Glaxo Company, Macleods Pharma, Ranbaxy Pharma, Torrent Pharmaceuticals, TCS etc.. etc.. etc..

    << ENQUIRE TODAY >>

    Scope of GIRA Courses in RA/QA/QC:
    · Adds on skills to your CV
    · Higher opportunities for Jobs
    · Updation of knowledge- A key to Successful Career
    · Get Promoted to Higher levels

    CONTACT :

    Global Institute of Regulatory Affairs,
    Office C5 and C6, Empire Estate,
    Chinchwad, Mum- Pune Highway,
    Near Premier Company,
    Pune- 411019
    Mob/ Tel: 9595 750 750/ 020- 4670 4472
    Web: www.regulatoryinstitute.com
    email: info@regulatoryinstitute.com
    Blog: www.regulatoryinstitute.com/blog

  • Walk in interview for establishment of Viral Research Diagnostic Laboratory for the post of Research Scientist, Lab Technician

    Pt B D Sharma PGIMS, Rohtak invites to appear in walk-in-interview on 27/02/2015 for filling up the following posts as per prescribed eligibility & @ salary fix p.m. mentioned below in ICMR/DHR sanctioned project entitled to develop a Medical college Level Viral Research Diagnostic Laboratory (VRDL) at Pt B D Sharma PGIMS, Rohtak.

    Post: Research Scientist, Lab Technician

  • Opening to work as Clinical Data Manager I in PPD Pharmaceuticals

    PPD is a leading global contract research organization providing discovery, development and post-approval services as well as compound partnering programs. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 32 countries and more than 9,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help its clients and partners maximize returns on their R&D investments and accelerate the delivery of safe and effective therapeutics to patients.

    Post: Clinical Data Manager I - Strong UAT & mentoring experience required - Bangalore-119056

  • Career as Medical Transcriptionist and Proof reader/editor in MedTek.Net | Only experienced candidates can apply

    MedTek.Net is one of the leading Healthcare BPO providers in India. Medtek.net is 14+ years old company. Medtek.net is subsidiary of Medtek.net Inc, California, USA.We provide Medical Transcription and Medical Coding services to several Healthcare Providers and Organizations in USA. We are operating from Ameerpet and Tarnaka in Hyderabad. We also have a branch in Vijayawada.

    Post: Medical Transcriptionist and Proof reader/editor

  • Required for Consultant - HLS-Pharma in Wipro

    Post: Consultant - HLS-Pharma (T342947)

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  • Merit scholarships for international students enrolled at Universität Hamburg

    International students and first-degree graduates with good to excellent academic achievements can apply for monthly scholarships of up to EUR 650. The maximum funding period is twelve months.

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  • Opening for Senior Medical Writer in Parexel

    PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.

    Post: Senior Medical Writer

  • Multiple vacancies in TMH | Opening for the posts of Pharmacist, Scientific assistant

    The Tata Memorial Hospital was initially commissioned by the Sir Dorabji Tata Trust on 28 February 1941 as a center with enduring value and a mission for concern for the Indian people.
    In 1952 the Indian Cancer Research Centre was established as a pioneer research institute for basic research - later called the Cancer Research Institute (CRI). In 1957 the Ministry of Health took over the Tata Memorial Hospital. The transfer of the administrative control of the Tata Memorial Centre (Tata Memorial Hospital & Cancer Research Institute) to the Department of Atomic Energy in 1962 was the next major milestone. The Tata Memorial Hospital and Cancer Research Institute merged as the two arms of the Tata Memorial Centre (TMC) in 1966 as a classic example of private philanthropy augmented by Government support with a mandate for Service, Education & Research in Cancer.

    Post: Pharmacist, Officer-in-charge, Scientific assistant

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