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Showing posts with label Jobs in Bangalore. Show all posts
Showing posts with label Jobs in Bangalore. Show all posts

Friday, 14 October 2016

Job Description

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    Overall Purpose of the job

    Supports PSSR team in medical assessment of cases produced by Accenture SER ensuring accuracy, internal consistency, uniformity, and compliance with regulatory commitments and expectations.

    Responsibilities/ Authorities

    Participates on project teams, task forces and/ or working groups to identify opportunities for strategic alignment of quality and compliance processes and process improvement initiatives.

    Supports/ promotes accuracy, internal consistency, uniformity, and compliance with regulatory commitments and expectations.

    Supports all the internal quality improvement initiatives.

    Provides medical advice and insights to Therapeutic Area colleagues to improve the quality, consistency, accuracy, and clinical relevance of safety reports.

    Supports PSSR Quality Assurance activities, addressing observations related to medical assessment, as appropriate. Ensure consistency and quality of the medical assessment process.

    Proactively mentor Therapeutic Area colleagues to foster an environment of trust, understanding, learning, and development.

Wednesday, 12 October 2016

At Indegene, we look to change healthcare for the better. Being an Indegene employee is not just doing a job, but it is about real contribution and outcomes. We are a global team of over 1,200 employees across 14 global locations. Our singular focus is to deliver real outcomes that are measurable, impactful, and sustainable. This has made us a recognized global leader and partner to some of the largest and most respected healthcare organizations.
Job Title : Analyst Research Analytics & Insights (HEOR)

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Monday, 10 October 2016

Job Description

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    Walk-In Drive for Clinical Research Associate15-Oct-16, Saturday at Apotex Research, Bangalore Campus.


    Apotex Research Private Limited (ARPL) based at Bangalore is engaged in in the development, bio-clinical evaluation, manufacturing, and distribution of safe and efficacious generic pharmaceutical formulations for the global market .
    Apply now


    Inviting Applications for the position.


    Interview Venue :- Apotex Research Private Limited, Plot No. 1&2, Bommasandra Industrial Area, 4th Phase, Jigani Link Road, Bangalore - 560099. Gate No. 1

Tuesday, 4 October 2016

Job Description

Image result for clinical trials

    The Clinical Research Associate will perform the following activities:
    To successfully conduct the listed site visits as required by client/study -- PreStudy Site Selection, Site Initiation, Interim Monitoring, Site Close out
    Meet with Clinical Investigators and staff prior to study initiation to ensure all aspects of the study are understood by the investigator and staff. If required train the study site team
    To confirm the appropriateness of the site for the study in all aspects and ensure that all documentation required to initiate the study is complete
    Monitor study progress to assure compliance with protocol requirements, FDA regulations and Good Clinical Practice by conducting site visits as directed by the Sponsor/CRO & NMI SOPs
    Monitor and track patient enrollment and study progress
    Perform site monitoring visits to include review of source document, case report form, ICD, Patient Diary, Investigator Site Binder, other documents as applicable
    Ensure the timely accurate and complete collection and submission of study data.
    Identify, address, and resolve issues and problems as they might occur.
    At study completion:
    Ensure collection of all data and remaining study supplies for return to the Sponsor/CRO
    Ensure that appropriate study documents are complete and properly filed
    Archival with Inventory list of Source documents/ CRFs/ CTM/ Others at site
    Prepare the site for possible Regulatory/ FDA inspection
    Prepare the site for possible Internal and/or Client Audits

Job Description

Image result for kelly services


    Looking for  Pharmacovigilance Writer

    Required

    PSUR

    DSUR

    PADER

    PBRER

    Aggregate Report Writer
    Company Profile:
    Kelly Services India Pvt. Ltd.

    Leading CRO

Monday, 3 October 2016

Incorporated in the year 1994, Syngene International is one of India’s premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area.
Job Title : Research Investigator in Biotransformation
Experience : 0 – 5 Years

Location : Bengaluru/Bangalore


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Click here

Friday, 30 September 2016

Applications are invited from the eligible candidates for filling up the post of Two Posts of “Senior Research Fellow” and Two Posts of “Project Trainee” on contract basis for the DBT funded project – I entitled “A multi centric study to develop comprehensive molecular genetic panels for glioblastoma personalized therapy”
DBT Project –II entitled “ Unraveling genetic and epigenetic landscape of gliblastoma: Insights into the therapy resistance and recurrence “Programme support on molecular Neuro-Oncology (Phase II)”  under Dr. Vani Santosh, Professor & Head Department of Neuro Pathology & Principal Investigator.


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Tuesday, 27 September 2016

Job Description


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    Responsibilities/Authorities : 

    1.Prioritise Data Entry activities for Cases by reference to the Date Receipt in accordance with SOPs and Guidelines;
    2.Data entry of safety information, including relevant medical history and laboratory data and therapy dates into the applicable Global Safety Database in accordance with Guidelines and SOPs;
    3.Validate data consistency and make any corrections as needed;
    Submit to Case Safety Reports for scientific and medical evaluation;
    4.Review responses to queries when received and update the Global Safety Database as required;
    5.Document any amendments to the Data Entry Conventions and agree these with the client Functional Lead, prior to their implementation;
    6.Participate in clinical study reconciliation activities, as requested by client; and
    7.Issue reconciliation listings as requested by client to the relevant Connected Entity and to client.

    Requirements 

    Fresher's also can apply with B.pharma/M.pharma/BDS/Pharma D from 2014,2015,2016 passed out.
    Healthcare degree preferred;
    For Experienced: 

    A minimum of 2 years Pharmaceutical or Clinical experience is preferred;
    1.Experience with MS Office products;
    Knowledge of coding applications, databases, processes and tools is preferred;
    2.Experience in researching information utilizing available resources including publications and the World Wide Web;
    3.Effective communication, organisation and time management skills;
    4.Good interpersonal skills and the ability to operate effectively in an international environment;
    5.English language (written) proficiency must.
    6.Thorough knowledge of medical terminology;
    7.Computer proficiency and ability to work in specific databases;
    8.Excellent written and verbal communication skills is a must
    NOTE :
    Candidates from Bangalore preferred.
    candidates should be flexible to work in shifts.

    Apply now

Monday, 26 September 2016

Job Description


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    Immediate Openings for IP-DRG Medical Coding @ Vee Technologies 
    Job Description: 

    1+ Years of experience in IP-DRG Coding.

    Coding certification like CIC, CPC, CCS, CPC-H, CCS-P. is added advantage.Apply here

Job Description

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  • To provide medical support to marketing team in strategizing brand plans and sales team.
  • Providing scientific and medical input to  Product Management Team for development of visual aid, LBLs, Recent guidelines, Treatment algorithms, Reference folders and patient education literature.
  • Conduct medical and orientation programme on Anatomy, Physiology , various related Clinical conditions and Product based knowledge to newly inducted sales employees.
  • To develop Protocol, CRF's and other trial related documents, coordinating with Investigators ethical committee submission for all the Phase IV, PMS and Investigators initiated studies. 
  • To meet KOL's and Investigators to develop a mindspace for Biocon and provide scientific support.

Saturday, 24 September 2016

It is a Fortune 500 company and the world’s largest provider of biopharmaceutical development and commercial outsourcing services with a network of more than 32,000 employees conducting business in approximately 100 countries
Post: PV-Operation Specialist

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Walk in interview Date : 24th September, 9:00 am at Prestige Technology Park II, Etamin Block  (Building B3), Sarjapur-Marathalli Outer Ring Road, Bangalore – 560103
Micro Labs, one of the fastest growing pharmaceutical companies in India with Global operations in over 60 countries. We enjoy a strong presence in various segments like Cardiology, Opthalmology, Psychiatry, Dermatology, Diabetology etc. with most of its brands among TOP 5 in their respective category.
DesignationOfficers/executives/assistant Manager -quality Assurance - 5 Opening(s)
Job DescriptionHands on experience in APQR, Calibration, IPQA- Manufacturing, QMS, Qualification and Validation
Desired ProfileHands on experience in APQR, Calibration, IPQA- Manufacturing, QMS, Qualification and Validation
Experience2 - 7 Years
Industry TypePharma / Biotech / Clinical Research


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Friday, 23 September 2016

Biocon is a research-driven, global healthcare company with a strong matrix of capabilities along the biopharmaceutical value chain. Focusing on unmet medical needs in cancer, diabetes and inflammatory diseases, it offers novel therapies on a platform of affordable innovation. Biocon together with group companies employs more than 2500 employees with approxmimately Rs 1,000 crore turnover and is expected to grow further during the current financial year.
Post : Executive / Sr. Executive

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Walk In Interview at Biocon Campus, 20th KM, Hosur Road, Electronic City, Bengaluru Sep 25, 2016 (9AM - 2PM)
Job Description :
Due to continued growth, PPD is expanding our Clinical Data Management department in Smolensk. This is an exciting opportunity to join a multinational American based CRO that is growing and expanding in Russian Federation. Joining our global clinical Data Management team, we offer more than regular Clinical Data Management. We bring a deep understanding of the science of disease and compounds, as well as provide valuable upfront study design and comprehensive planning assistance to our global client base.

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Key Responsibilities :

  • The objective of a Clinical Data Associate II is to perform advanced aspects of the data cleaning process with a high level of accuracy and in accordance with GCPs and SOPs/WPDs, in order to assess the safety and efficacy of investigational products and/or medical devices.
  • Clinical Data Associate IIs are expected to perform the tasks of a Clinical Data Associate I with increased efficiency, while maintaining a high level of accuracy, and to work more independently.
  • In addition they will be expected to perform data management activities such as Serious Adverse Event and Third Party Vendor reconciliations as well as Data Listing reviews.

Thursday, 22 September 2016

Syngene Hiring For the Post of Research Associate / Senior Research Associate – Microbiology


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Job Description :
1.Execution of experiments related to Microbiology
2.Supporting Raw material for procurement for projects
3.Data Preparation and Submission for Review
4.Equipment handling and maintenance (lab support)
5.Literature Survey
Desired Profile
1.Sound knowledge of Microbiology: Basic and Applied
2.Knowledge of working in food/consumer care Microbiology
3.Innovative thinking and adaptation to changing priorities

Apply now
Incorporated in the year 1994, Syngene International is one of India’s premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities.
Job Title : Cell Biology Scientist
Experience : 2 – 6 Years
Location : Bengaluru/Bangalore
No of Openings : 2
Eligiblity : PG – M.Tech – Bio-Chemistry/Bio-Technology, M.Sc – Bio-Chemistry, Microbiology

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Job Description :

  • Should have sound knowledge in Cell Biology
  • Generation of stable cell lines.
  • Transcient transfection
  • Flow Cytometry
  • Cell Freezing
  • ELISA
  • Lentiviral transduction


Wednesday, 21 September 2016

Job Description :
1.Execution of experiments related to Microbiology
2.Supporting Raw material for procurement for projects
3.Data Preparation and Submission for Review
4.Equipment handling and maintenance (lab support)
5.Literature Survey

Image result for biocon


Apply now

Syngene Hiring For the Post of Research Associate / Senior Research Associate – Microbiology


Image result for syngene

Job Description :
1.Execution of experiments related to Microbiology
2.Supporting Raw material for procurement for projects
3.Data Preparation and Submission for Review
4.Equipment handling and maintenance (lab support)
5.Literature Survey
Desired Profile
1.Sound knowledge of Microbiology: Basic and Applied
2.Knowledge of working in food/consumer care Microbiology
3.Innovative thinking and adaptation to changing priorities

Apply now
Job Description
Main Duties & Responsibilities:   
- Perform sampling, testing and related documentation for Raw materials, Finished Goods and Packing materials.  
- Outsourcing of raw materials for testing and follow up.  
- Follow Quality systems like GLP, GDP and OOS.  
- Preparation of QC SOP’s  
- Preparation and standardization of Volumetric Solutions and reagents     Handing of instruments like FT-IR, UV-Spectrophotometer, Data color, Viscometer, Autotitrator etc



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Job Description

Image result for vee tech

    Immediate Openings for IP-DRG Medical Coding @ Vee Technologies 
    Job Description: 

    1+ Years of experience in IP-DRG Coding.

    Coding certification like CIC, CPC, CCS, CPC-H, CCS-P. is added advantage.

    Specialty : IP-DRG
    Experience   : 1- 6 Years.
    Designation : Medical Coder/ Sr.medical Coder/QA & TL
    Location      : Chennai / Bangalore/ Salem

    Attractive salary & joining bonus for the immediate joiner's.
    Interested Candidate Call Immediately to the below contact number

    Regards,
    Ramesh - HRD
    9443238706
    mail: ramesh.m@veetechnologies.com
    Apply now
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