Opportunity for Medical Coding Analyst- Freshers Only (Non Certified ) @ UnitedHealth Group "D8"

Opportunity for Medical Coding Analyst- Freshers Only (Non Certified ) @ UnitedHealth Group

Designation     Medical Coding Analyst- Freshers Only (Non Certified )
Job Description     Purpose of Job This process works on assigning appropriate codes against the diagnosis, procedures, supplies and tests as mentioned in charts received from hospitals. The associate need to assign correct ICD, CPT and supply codes. Job Responsibilities-Assign correct ICD, CPT and Supply codes for the charts received -Adherence to state and federal compliance policies and  Client SLAs-Assist the prospective team with special projects and reporting
Desired Profile     Required Qualifications -Educational Qualification - BHMS/ BAMS/ BUMS/ BPT/ MPT/ B. Sc Nursing -Knowledge of US Healthcare and coding desirable -Attention to detail & Quality focused. -Good Analytical & comprehension skills. Preferred  Qualifications -Health Insurance knowledge, managed care experience preferred -Claims processing experience is helpful-Medical record familiarity is preferred
Experience     0 - 1 Years
Industry Type     Pharma / Biotech / Clinical Research
Role     Claims Executive
Functional Area     Financial Services, Banking, Investments, Insurance
Education    

UG - Any Graduate - Any Specialization

PG - Any Postgraduate - Any Specialization

Doctorate - Any Doctorate - Any Specialization, Doctorate Not Required
Compensation:      Not disclosed
Location     Hyderabad / Secunderabad

Click here to apply

Opportunity to work as Clinical Research Associate @ Manipal Acunova Ltd. "D7"

Opportunity to work as Clinical Research Associate @ Manipal Acunova Ltd.


Job Description

    The responsibility of a Clinical Research Associate (CRA) is to perform all clinical monitoring aspects of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, and data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines.

        Preparation of Site feasibility questionnaire, conducting the feasibility and reporting to PM

    Preparation, conduct and reporting of site selection visits

    Negotiation & obtaining Investigator agreement on site budget, payment to the sites

    Development/Local adaptation of study specific documents (ICF, CRF prints, Study logs), translations of the documents

    Procuring essential documents from sites, their QC and filing in a timely manner and updating project tracker or sending the documents to PA for filing in a timely manner

    Maintenance of TMF and Site specific file

    Scanning & uploading documents into shared drive

    Transmission of documentation into project files

    Preparation of regulatory dossier, regulatory submission and follow-up.

    Preparation of EC dossier, EC submissions and follow-up

    Co-ordinating arrangements for the investigators meeting, acting as a host for this meeting

    Development of meeting materials along with required presentations for investigators meeting.

    Site initiation visit planning, preparation, conduct, report and follow-up of pending issues

    Co-ordinating the IP request between sites and pharmacist/vendor/sponsor

Salary: Not Disclosed by Recruiter

Industry: Pharma / Biotech / Clinical Research

Functional Area: Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology

Role Category:R&D

Role:Clinical Research Associate/Scientist
Keyskills
Clinical Research clinical trial clinical research associate cra clinincal monitor
Desired Candidate Profile

Education-

UG: B.Pharma - Pharmacy

PG:M.Pharma - Pharmacy

Doctorate:Any Doctorate - Any Specialization, Doctorate Not Required

    Worked in OPHTHALMOLOGY or ONCOLOGY or DIABETES studies Clinical Studies I-IV

    Ability to interact professionally with clients/vendors

    Excellent interpersonal, verbal and written communication skills and ability to work in a team

    Effective time management skills and prioritize tasks to manage study timelines

    Strong computer and internet skills including knowledge of MS-Office products such as Excel, Word etc, sound presentation skills

    Willing to travel a minimum of 65% on average

Company Profile:

Manipal Acunova Ltd.

Ecron Acunova provides end-to-end services for Phase I - IV clinical research, including Clinical Trial Management, Clinical Data Management, PK/PD services and Central Lab. Ecron Acunova has research facilities in Asia as well as an established presence in various parts of Europe and the United States. As regional experts, we operate each region as a priority market. Our European HQ is in Frankfurt, Germany, in the United States our HQ is in Princeton, NJ and our Asian HQ is in Bangalore, India. We offer clinical development services to the pharmaceutical, biotechnology, nutritional, device and medical diagnostics industries. Our service quality, therapeutic expertise and global reach have allowed us to grow rapidly, building a list of demanding clients. We provide an attractive package of services coupled with the ability to rapidly conduct clinical trials utilizing a world class delivery platform.
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Opening for Clinical Data Manager @ Novartis Healthcare Pvt. Ltd. "D6"

Opening for Clinical Data Manager @ Novartis Healthcare Pvt. Ltd.


Job Description



Coordinate Clinical Data Management (CDM) activities for several protocols and CDM projects. In particular: Serve as Project CDC for large projects or multiple smaller projects providing professional Data Management input to global clinical teams. Responsible for timelines and quality of the CDC deliverables, including eCRF, EDC database set up and database locks, for the assigned projects and/or trials. Maintain clinical trial study workbooks Perform database lock preparation activities in time for interim and final database lock. Generate summary reports and listings for the Clinical Department Provide professional CDM input to Clinical Trial Team(s). Coordinate trial activities with biostatistician, prorgammers, and clinical team Provide CDM training to clinical trial team members, site personnel and external site monitors. Serve as Project CDC for projects outsourced to CROs. Complete activities within the time frame of established metrics. Ensure appropriate tracking systems (e.g. CTMS) are up to date and accurate. Adhere to SOPs and guidelines. Identify problems, analyze them, and suggest solutions. Assist in authoring, and participate in the review of CDM procedures and guidelines. Contribute towards and participate on CDM projects. Author, review and/or execute test plans for CDM programs.

Salary: Not Disclosed by Recruiter

Industry: Pharma / Biotech / Clinical Research

Functional Area: Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology

Role Category:R&D

Role:Clinical Research Manager
Keyskills
Clinical Data Management CDM Clinical Trial eCRF EDC
Desired Candidate Profile

Education-

UG: Any Graduate - Any Specialization

PG:M.A - English

Doctorate:Doctorate Not Required

    Minimum requirements:
    Master Degree English Relavant Experience in Data Mgr.

Company Profile:

Novartis Healthcare Pvt. Ltd.

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 us one of the most rewarding employers in our field.
Click here to apply

Openings for Life Science candidates as Research Associate Posts @ Piramal Health Care "D5"

Openings for Life Science candidates as Research Associate Posts @ Piramal Health Care



Piramal Discovery Solutions (formerly o2h) provides a world class integrated drug discovery services platform from our state-of-the-art research centre in India. PDS's delivery model has a proven track record of providing a step change in the effectiveness of drug discovery for a range of global pharmaceuticals and Biotechnology companies operating at the forefront of drug discovery. PDS understands that early and intensive evaluation of the molecules based on thorough communications and rapid decision-making will lead to a high throughput of successful drug-like compounds.

Job Title : Research Associate-adl/senior Research Associate

No of Openings : 25

Qualification : M.Sc Life Science

Experience : 1-6 years

Job Description :

    LC-MS / HPLC Method Development(NCE)
    Analytical Method Development of NCE independently.
    Interpretation of LCMS & NMR Spectra.
    Isolation and characterization of products.
    Responsible for troubleshooting of Instruments in case of problems.
    Calibration of Analytical Instruments.
Click here to apply

Opening for Research Associate Posts for Life Science Graduates @ INTAS "D4"

Opening for Research Associate Posts for Life Science Graduates @ INTAS


Experience spanning three decades in healthcare, with a wide range of formulations to meet the needs of ailing humanity, Intas Pharmaceuticals headquartered at Ahmedabad (India), is now a force to reckon with, in the global pharma horizon. With expertise in a range of formulations, from tablets to injectables to newer drug delivery systems, Intas is currently ranked 17th among the Indian Pharma majors. A variety of initiatives in Research and Development, patents and ANDA filing, NDDS, quality manufacturing support, along with approvals by regulatory authorities of many countries has made Intas a global healthcare provider. Pioneering efforts in providing medications for both chronic and acute medical conditions, has truly led Intas live up to its corporate line �Expressions for a Healthy Life.

Job Title : Research Associate

Qualification : B.sc/M.Sc Lief science

Experience : 1-6 years

Job Description :

    Complete analysis of raw material, finished products & stability samples.
    Analytical method development - Assay, Related substances & Dissolution.
    Analytical method validation - Assay, Related substances & Dissolution.
    Analytical method transfer - Assay, Related substances & Dissolution.
    Operation & Calibration of various Instruments.
Click here to apply

Opportunity for Microbiology Graduates to work as Executive - QC Posts @ Piramal Health Care "D3"

Opportunity for Microbiology Graduates to work as Executive - QC Posts @ Piramal Health Care

Piramal Enterprises - Healthcare Domain is one of the largest custom manufacturing companies in the world that provides flexibility and scalability of operations. We have created a vast network of contract development and manufacturing facilities located in North America, Europe and Asia that offers a multitude of services that cover the entire drug-cycle, from development and commercial manufacturing to off-patent supplies of Active Pharmaceutical Ingredients (APIs) and formulations. Our network enables us to deliver benefits by strategically placing projects to take advantage of low costs, local supply chains and specific customer/ market requirements. This division features among the top 10 contract drug manufacturers in the world. Piramal has forayed into the healthcare space in 1988 with a move that was contrarian at that time as most pharmaceutical players were exiting India due to the existing business climate. It has been 25 years, and we have established ourselves as one of the most recognizable and respected names in the pharmaceutical industry.

Job Title : Executive - QC (Microbiology)

Qualification : B.sc/M.Sc Microbiology

Experience : 5-8 years

Job Description :

    Setting the analysis priorities based on the production planning in Microbiology section.
    Analysis of Water, Raw Materials, Finished products and Crossover Studies in Microbiology section (If, requiried).
    To allocate regular shift analysis work to the staff reporting to him and review of Analyst Handbooks, Analytical Raw Data, Equipment usage log books, Standard Reconciliation data, Column reconciliation details etc. after completion of the activity.
    Responsible for Balance Daily Verification, pH Meter Daily Calibration, Milli-Q Water Daily verification, Daily Temperature and Relative Humidity monitoring records.
    Responsible for planning of Calibrations and Preventive Maintenance activities as per the schedule in Microbiology section.
Click here to apply

Openings for QA/QC Executive Posts @ Marksans Pharma "D2"

Openings for QA/QC Executive Posts @ Marksans Pharma



We have established world-class manufacturing facilities by leveraging state-of-the-art technology, incorporating best practices and adhering to stringent regulatory compliances. Our plants are approved by prestigious US FDA, UK MHRA, Australian TGA and other foreign health authorities. Our R&D capabilities include dossier development, chemical synthesis, process optimization, formulation development, analytical development and conducting stability studies. We have a team of over 50 experienced scientists specializing in formulation development and analytical development. We possess end-to-end capabilities – from Lab scale development to Pilot scale up and from commercializing the product for large scale manufacturing to marketing globally. The company has achieved global recognition within a very short span of time and has major global expansion plans for the near future.

Job Title : QA/QC Executive

Qualification : B.sc/M.Sc/M.trech/B.Tech Life Science

Experience : 0-3 years

No of Openings : 20

Job Description :

    Pharma / Biotech / Clinical Research
    Production , Manufacturing , Maintenance
    Quality Assurance/Quality Control Executive
Click here to apply

Opening for FRESHERS as Quality Control @ Mylan "D1"

Opening for FRESHERS as  Quality Control @ Mylan


At Mylan, we mean it when we say we work every day to provide access to high quality medicines to the world’s 7 billion people. If you are unconventional, relentless and passionate. If you believe in doing what’s right, not what’s easy. If you are a doer and have a passion for serving others, we want to talk to you.At Mylan, each person has the ability to make a difference. From the providers who sell and market our products to the producers who develop and manufacture them and finally to our business partners who support the providers and producers, we all have a mission critical role.

Job title : Officer - Quality Control

Qualification : B.sc/M.Sc Life Science

Experience : 0-2 years

Job description :

    Test raw materials, blend intermediates and finished product to ensure a quality product that is safe to release to the public
    Review and process data. Interpret test results and ensure that they meet specifications. Enter data into the computer, maintain instrument logbooks
    Act as a resource to team members and other Chemists
    Act as back-up in a team leader’s absence

Click here to apply

Opening for AR Callers - Medical Billing @ JMA IT Solutions Pvt. Ltd. "D8"

Opening for AR Callers - Medical Billing @ JMA IT Solutions Pvt. Ltd.

Hiring for leading US healthcare BPO in and across location!!!
Designation     AR Callers - Medical Billing - Chennai, Bangalore, Mysore, Cochin, Hyd - 50 Opening(s)
Job Description     Medical billing - Quality analyst/Senior AR Callers/AR Callers!!!

Position: Quality Analyst, Senior AR Caller, AR Caller.

Greetings from JMA IT Solutions,
We are hiring for experienced Quality analyst/ Senior AR Callers/ AR Callers for leading US Healthcare BPO in Chennai, Bangalore, Mysore, cochin, Trivandrum & Hyderabad

Job Description:

Candidates should have min 6 months experience in AR Calling process from Medical Billing (US Healthcare process)

Skills:
should have experience in Revenue cycle Management (RCM)

Insurance calling
Patient calling
AR follow-up
Denial Management

Experience:

1-6 yrs in AR Calling - Medical Billing

Salary: 30-40% hike from Current salary best in the industry.

Work location: Chennai, Bangalore, Mysore, cochin, Trivandrum & Hyderabad

Note: Telephonic interview will be arranged. Immediate joiners will get joining bonus 10K

Interested candidates please call to 9962056248 (Sharmila lakshmanan) for more details.

Thanks & Regards,
Sharmila Lakshmanan
HR Team,
JMA IT Solutions Pvt. Ltd.
Mobile: 9962056248
Email: sharmila@jmait.com
Web: www.jmait.in | www.jmait.com


Desired Profile     Please refer to the Job description above
Experience     1 - 6 Years
Industry Type     BPO / Call Centre / ITES
Role     Associate/Senior Associate -(NonTechnical)
Functional Area     ITES, BPO, KPO, LPO, Customer Service, Operations
Education    

UG - Any Graduate - Any Specialization

PG - Any Postgraduate - Any Specialization

Doctorate - Any Doctorate - Any Specialization
Compensation:      1,50,000 - 4,50,000 P.A. Best in Healthcare industry
Location     Chennai, Bengaluru/Bangalore, Hyderabad / Secunderabad, Ernakulam / Kochi/ Cochin, Trivandrum, Mysore
Keywords     arcaller arcalling arexecutive ar associate rcm medical billing credit and collections caller calling healthcare denials executive ar
Contact     Sharmila lakshmanan
JMA IT SOLUTIONS PRIVATE LIMITED
Telephone     9962056248
Email     sharmila@jmait.com
Click here to apply

Opening for Microbiologist @ dr. ahujas pathology and imaging centre "D7"

Opening for Microbiologist @ dr. ahujas pathology and imaging centre

Job Description

Send me Jobs like this

    Full time MD microbiologist familiar with NABL/15189 guidelines

Salary: 9,50,000 - 12,00,000 P.A

Industry: Medical / Healthcare / Hospitals

Functional Area: Medical , Healthcare , R&D , Pharmaceuticals , Biotechnology

Role Category:R&D

Role:Microbiologist
Keyskills
MD Microbiology md microbiology
Desired Candidate Profile

Education-

UG: MBBS

PG:M.S/M.D - Microbiology

Doctorate:Doctorate Not Required

Click here to apply

Govt Job for B.sc/M.Sc Life Science @ Indian Pharmacopoeia Commission "D6"

Govt Job for B.sc/M.Sc Life Science @ Indian Pharmacopoeia Commission

Indian Pharmacopoeia Commission (IPC) is an Autonomous Institution of the Ministry of Health and Family Welfare, Govt. of India. IPC is created to set standards of drugs in the country. It’s basic function is to update regularly the standards of drugs commonly required for treatment of diseases prevailing in this region. It publishes official documents for improving Quality of Medicines by way of adding new and updating existing monographs in the form of Indian Pharmacopoeia (IP). It further promotes rational use of generic medicines by publishing National Formulary of India.

Position I

Job Title : Documentation & Publication Assistant

Qualification : B.sc/M.Sc Life Science

Experience : 2 years

Job Description :

    Maintenance of Publication
    Hindi & English typing technical writing
    typesetting page making, layout & design, edition and proof reading etc. of official publications of IPC.

 Position II

Job Title : Library & Information Assistant

Qualification : B.sc/M.Sc Life Science

Experience : 2 years

Job Description :

    Maintenance of Library & Information centre/documentation
    accessioning of documents/classification & cataloguing of documents/indexing & abstracting of periodicals/compilation of CAS/SDI /data entry /newspaper clipping/reference service. technical writing etc.
     related correspondence there to and any other work assigned from time to time by concerned officer.
Click here to download application form

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Walkin Interview at Indore on 01st March 2015 for EXECUTIVES/ OFFICERS/ ASSOCIATE @ Cipla "D5"

Walkin Interview at Indore on 01st March 2015 for EXECUTIVES/ OFFICERS/ ASSOCIATE @ Cipla

Job Description

Cipla
requires
for its Sterile & Non-sterile formulation plant at
ISEZ Pithampur ,Indore

EXECUTIVES/ OFFICERS/ ASSOCIATE
In

Sterile Production
We are looking for appropriately qualified candidates with 1 to 10 years of relevant in Production of Nasal Spray, Aerosol, Eyedrop, FFS, Injectable, LVP, SVP, ophthalmic and Parenterals with a reputed Pharma company should have regulatory exposure.

Technician/ Machine Operators
Appropriately Qualified HSC, ITI and Diploma candidates with minimum 2 years of relevant experience in Nasal Spray, Eyedrop, Aerosol, FFS, Injectable, LVP, SVP, ophthalmic and Parenterals Filling, Manufacturing, and Packing operating latest machineries.

Tablet Packing / Production
We are looking for in B. Pharma/HSC/ ITI / DME qualified candidates with 1 to 5 years of relevant in Tablet production and Packing with a reputed Pharma company should have regulatory exposure

Quality Control
We are looking for appropriately qualified candidates with 1 to 5 years of relevant in Quality Control with a regulated Pharma company should have exposure in all sophisticated QC Instruments & documentation.

Microbiology
We are looking for appropriately qualified candidates with 1 to 5 years of relevant experience in microbiology with a regulated Pharma company.

Stores
We are looking for appropriately qualified preferably B.sc candidates with 1 to 10 years of relevant in Stores with a regulated Pharma company

Interested candidates should meet Mr Mahendra Singh Rathore Mr Ashutosh Singh Tomar with a recent copy of the bio-data, a colour photograph and CTC Statement/Salary slip on March 01, 2015 (Sunday) between 9:00 am and 5:00 pm at the address mentioned below:

Christian Eminent College
06-A Press Complex
Behind Dainik Bhaskar
AB Road, Indore (MP)

Click here for more details

Opportunity for freshers to work as Medical Officer @ Piramal Swasthya Management and Research Institute (PSMRI) "D4"

Opportunity for freshers to work as Medical Officer @ Piramal Swasthya Management and Research Institute (PSMRI)

Piramal Swasthya Management and Research Institute (PSMRI) is a registered society based in Hyderabad, Andhra Pradesh. PSMRI is supported by Piramal Foundation and works towards making healthcare accessible, affordable and available to all segments of the population, especially those most vulnerable.
Designation     Medical Officer - 10 Opening(s)
Job Description     Receiving calls and answering them as per defined protocol Maintaining and following all the quality parameters.
Flexibility to work in all the shifts of 7 hrs each.
Ability to do night duty min of 4 per month of 10hrs each.
Advice given to callers should be based on the information given in the application following Algorithms and Disease summary.
Desired Profile     Please refer to the Job description above
Experience     0 - 5 Years
Industry Type     Medical / Healthcare / Hospitals
Role     Outside Consultant
Functional Area     ITES, BPO, KPO, LPO, Customer Service, Operations
Education    

UG - MBBS - Medicine

PG - Any Postgraduate - Any Specialization

Doctorate - Any Doctorate - Any Specialization
Compensation:      3,25,000 - 3,50,000 P.A
Location     Hubli
Keywords     Medical advice
Contact     Mr. Shadrak
PIRAMAL ENTERPRISES LTD
Telephone     9886725103
Website     http://www.piramal.com

Click here to apply