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Thursday 30 June 2016

Govt Job : Exclusive R&D Job @ Central Sericultural Germplasm Resources Centre, Central Silk Board

Applications are invited for
one Junior Research Fellow
purely on temporary
basis for CSB p
roject
"PIE-3566:
Eva
l
uation of coreset of mulberry g
e
rmplasm for
physi
o
l
o
gical
eff
iciency
a
nd leaf qua
l
ity
"
Duration:
3 years or closure of project whichever is earlier
Place of Work:
CSGRC, Hosur,
Tamil Nadu
Age limit:
28 years
(Relaxable in case of SC/ST/OBC as per GOI rules on the l
ast date
of the receipt of application.
Essential Qualification:
Master degree in Agricultural Sciences/ Life Sciences /
Biotechnology with specialization in Plant Physiology or Plant Biochemist
ry
Fellowship :
Rs.16,000 p.m. fixed plus 10% HRA for NET (UGC/CSIR)/ GATE
qualified candidates otherwise Rs.12,000 p.m. plus 10% HRA.
The interested eligible candidates may send their application
to the following
address giving complete bio-data along with recent passport size
photograph and
photocopies of relevant certificates in support of qualification and expe
rience should
reach the undersigned on or before 09.06.2016. Short listed candidates will be c
alled for
interview at their own cost.

Life Science Candidates Apply For the International Bayer Scholarship Program



EHS Specialist I – Hazard Communication
The Hazard Communication Specialist supports all Thermo Fisher business divisions by completing hazard assessments, preparing hazard communication documents (safety data sheets and labels), assisting with safety data sheet distribution, and maintaining product information systems for knowledge management and compliance assurance.
The right candidate will have experience providing regulatory support for both internal and external customers, and is comfortable working closely with internal Product Management, Sales, and Project Management teams. We are looking for an individual with 2-3 years of experience in the Regulatory, Product Stewardship or EH&S field, with an emphasis on hazard communication requirements.​ Knowledge of domestic and international transportation classification is also required.
Essential Responsibilities:


  • Prepare globally compliant GHS format Safety Data Sheets (SDS) and container labels for Thermo Fisher's commercial and experimental products
  • Communicate with Thermo Fisher R&D staff to ensure detailed compositional and physical property data needed for the product's hazard assessment are provided.
  • Work with Thermo Fisher toxicologists to ensure product's hazards are adequately evaluated and addressed on the SDS and labels as needed.
  • Responsible for examining product formulation and documentation necessary for proper hazardous characterization
  • Determine U.S. and International transportation hazard classifications.
  • Understand laws and regulations (e.g. OSHA, GHS, REACH) governing SDS authoring, downstream chemical distribution, and hazardous chemical management within the Environmental Health and Safety industry
  • Maintain product updates in Thermo Fisher data repository (Agile)
  • Assist with management of SDS distribution tool.
Essential Requirements:
  • Requires a minimum of 2-3 years of relevant experience in Hazard Communication, experience with GHS, CLP-REACH and hazard assessments.
  • Bachelor’s degree in Toxicology, Chemistry, Biology or other life sciences; In lieu of degree a minimum of 2-3 years’ experience with SDS authoring or experience with product formulation development and chemistry or refining operations will be considered.
  • Requires strong analytical skills and ability to accurately manage large amounts of detailed information.
  • Ability to work comfortably in advanced MS-Excel and MS-Access.
  • Demonstrated ability to work in a team atmosphere and to work independently.
  • Demonstrated ability to learn complex databases
  • Demonstrated excellent communication skills, both oral and written
  • Able to communicate effectively with technical and non-technical personnel
  • Promotes understanding of customer requirements and expectations
  • Demonstrated ability of problem solving and decision making
  • Experience working with multiple customers
  • Reprioritizes work quickly to meet changing demands.
Preferred abilities:
  • Familiarity with Agile, E1, SAP, WERCS
  • Regional regulatory knowledge
  • Expertise with databases and advanced Excel functions

Biotechnology Faculty Recruitment 2016 @ B.S. Abdur Rahman University


B.S. Abdur Rahman Crescent Engineering College, which has now been upgraded as B.S Abdur Rahman University



Quality Coordinator Post Vacant @  General Mills | Apply Online




Job Details

Quality Coordinator I



We serve the world by making food people love.  As one of the world’s leading food companies, General Mills believes that food should make us better. Food brings us joy and nourishes our lives, connecting us to each other and the earth.  General Mills operates in more than 100 countries and markets more than 100 consumer brands, including Cheerios, Häagen-Dazs, Nature Valley, Betty Crocker, Pillsbury, Annie’s, Lara Bar, Yoplait and more. Headquartered in Minneapolis, General Mills had global net sales of US$17.6 billion during fiscal 2015.

We seek out the best talent, and then give them development resources, support and the chance to lead something big. Choosing a career with General Mills means joining a company where you can make a difference in the lives of millions of people. There is tremendous opportunity here for individuals who want to advance food through innovation and serve the world.
Specifications:
The heart of General Mills specifications systems is the PLM (Product Lifecycle Management) module of SAP. In order to ensure high quality and consistent manufacture of our products, details of raw materials and finished products are documented within PLM. This position is responsible for working on these specifications.
Ingredient Specifications
  • Manage new ingredients request process. Requires collaboration with R&D & Vendors.
  • Understand vendor status and manage creation of new vendors
  • Contact ingredient vendors to gather and review information such as Technical Data sheet, Nutritional information, & Religious/ dietary information for various category of Ingredients.
  • Handle Specification responses & ingredient surveys. Manage all vendor documents received
  • Handle highly confidential information from vendors and enter into General Mills’ SAP PLM system
  • Ensure vendor acceptance of changes and manage final notice process
  • Handle vendor rejections of Specs & communicate to ingredient category owners.
  • Maintain updated certifications (Kosher/ Organic)
  • Maintain updates Vendor contacts for all the GMI vendors
  • Handle tier one or simple Autonomous System Maintenance type project.
  • Back-up others under supervision on job tasks, as needed
  • Support US business teams on system testing’s after system upgrade or for new systems/applications
  • Identify ways to improve processes, systems and implement changes

Freshers Job : Trainee ( MSc. in Biotechnology/ Genetics ) Post Vacant @ NDDB


The National Dairy Development Board -- initially registered as a society under the Societies Act 1860 -- was merged with the erstwhile Indian Dairy Corporation.


IIT, Roorkee Hiring JRF / SRF | Qualification : Masters in Life Sciences, Botany, Biotech, Biochemistry


Applications are invited from Indian nationals only for project position(s) as per the details given below for the consultancy/ research project.


 


Massive Recruitment Drive @ Syngene For R&D Positions in Upstream & Downstream Process


Incorporated in the year 1994, Syngene International is one of India's premier contract research and manufacturing organizations .



Reliance Group Exclusively Hiring Biological Science Candidates For QA/QC Research Associate Post

“Your Leadership. Energising Reliance. India’s Future”

The Reliance Group is India's largest private sector enterprise, with businesses in the energy and materials value chain. Group's annual revenues are in excess of US$ 73bn. The flagship company, Reliance Industries Limited, is a Fortune Global 114 company and is the largest private sector company in India. Backward vertical integration has been the cornerstone of the evolution and growth of Reliance. Starting with textiles in the late seventies, Reliance pursued a strategy of backward vertical integration - in polyester, fibre intermediates, plastics, petrochemicals, petroleum refining and oil and gas exploration and production - to be fully integrated along the materials and energy value chain.

The Group's activities span exploration and production of oil and gas, petroleum refining and marketing, petrochemicals (polyester, fibre intermediates, plastics and chemicals), textiles, retail, infotel and special economic zones.

Reliance enjoys global leadership in its businesses, being the largest polyester yarn and fibre producer in the world and among the top five to ten producers in the world of major petrochemical products. Major Group Companies are Reliance Industries Limited, including its subsidiaries and Reliance Industrial Infrastructure Limited.

Short Description

Carry out assigned technical jobs of conducting experiments and upkeep of equipment/units laboratory/pilot plant and record data with diligence


Long Description

Analysis of nutrients in seawater

  1. Colorimetric estimation of nutrients such as Nitrate, Nitrite, Urea, Ammonia, Total phosphate, Orthophosphate, Sulphate, total nitrogen.
  2. Experience in measuring DO, pH, salinity, alkalinity, conductivity.
  3. Ability to write SOPs for the experiments carried out.
  4. Ability to authenticate values obtained by keeping internal standards

Skills Required (Knowledge and Skills)
Knowledge:

 A thorough knowledge in: Microbiological/ Biochemical techniques: colorimetry, polarography, centrifugation, titration, gravimetric analysis and microscopy.

Laboratory skills: In handling equipment pertaining to the above.

Field Skills:  Ability to collect water samples that would represent the entire raceway, smaller and larger ponds for analysis.

 Key Attributes (Experience and Qualifications)

  1. MSc Microbiology / biochemistry with good practical training
  2. Proficiency in domain knowledge.
  3. Ability to adapt to situations.
  4. Willing to collaborate and co-operate with co-workers.
  5. Experience in analytical techniques.
  6. Ability to get reproducible results.
  7. Knowledge in statistics.
  8. Data logging in excel sheets.
  9. A flair for instrumentation




Reliance has six Values and associated behaviors which are the essential and enduring tenets underpinning all decisions and way of life at Reliance and every employee is expected to abide by them. We are also committed to adhering to our candidate charter to deliver the best candidate experience.

Apply now

Clinical Data Specialist Post Vacant @ PRA Health Sciences


The story of PRA Health Sciences would naturally talk about how we’ve become one of the world’s largest CROs.  It would talk about our innovation and growth and would speak to our operational efficiencies and transparency.

 Overview

Provide timely and professional ongoing management of clinical trial data by identifying and resolving errors and inconsistencies in eCRF data to ensure consistently high standard database(s) with respect to cost, quality and timelines.

Responsibilities


  1. Provide professional DM input on Clinical Trial Team(s)
  2. Input to and review of clinical trial database design including User Acceptance Testing (UAT).
  3. Provide input for the Validation and Analysis Plan (VAP) meeting for the clinical trial, which includes taking an active part in the meeting, providing input in writing the study specific validation checks and necessary reports to ensure high quality and consistent data.
  4. Identify errors and inconsistencies; resolve them or initiate their resolution either via the field monitor or directly with the investigational site, to ensure high quality and timely database locks.
  5. Review and contribute to preparation of protocols, specifically related to the data management section, visit schema and study design with supervision.
  6. Prepare Case Report Forms (CRFs) and CRF completion Guidelines (CCGs), electronic or paper.
  7. Support and assist data management staff for allocated trials.
  8. Freeze and lock data as appropriate in time for statistical review, blinded interim quality review, interim and final database lock.
  9. Perform training on data management software and practices or trial specific  topics as required.
  10. May participate in preparation of training materials for data management activities and processes.
KPIs:
Meet established KPIs.  Timely and high quality completion of Data Management deliverables according to established objectives, including:  CRF Design, UAT of eCRF.  Fast and high quality Database Lock, EDC User Training.

Qualifications

  • Education (minimum/desirable):University or college degree in life science, computer science, pharmacy, nursing or equivalent relevant degree.
    Languages:Fluent English (oral and written).
    Experience/Professional requirement:
    1. Minimum of 2 years experience in drug development and at least 1 year experience in Data Management
    2. University Science Degree in life sciences, pharmacy, nursing or equivalent relevant experience.
    3. Excellent written and oral English skills
    4. Understanding of clinical trial methodology, GCP and medical terminology
    5. Good computer skills
    6. Good organizational and project management skills.
    7. Good communication and interpersonal skills
    8. Basic presentation and problem solving skills
    9. Ability to work well in a team with or without supervision

Wednesday 29 June 2016

Code MeDica is a proliferating healthcare training institute located in Bangalore. We are a Institute focused entirely on Medical Coding and Medical Billing.  Our in-depth healthcare training expertise enables us to provide end-to-end solutions to successfully resolve our students’s coding and  billing challenges.


We give a wonderful opportunity to Life Sciences students to develop a outstanding career in Healthcare industries. Healthcare industry is an emerging one in present scenario and is something which will keep on emerging in coming years.

Mission Statement

It is the Mission of our institute  to strengthen and promote excellence in medical coding, billing, and also for CPC certification.

Code medica is committed to prepare a highly skilled health workforce made up of health care professionals, health management and support workers.
It will strive to produce health care professionals who will integrate the advances in research healthcare industries with their best accuracy.
It will promote health services, which incorporate the latest advances in scientific knowledge in a manner that supports education for the benefit of the industry..

 Vision Statement

The institute aspires to attract the best of students by offering a variety of excellent programs supported by quality administration and student support services.
The institute aspires to be known for excellence and impact of its research on the educational milieu of the country  and the outcomes of healthcare.
 The University aspires to be an integral part of the community through transfer of knowledge, continuous dialogue with the country’s health care planners and enhanced community service.

“Join Us Today…Make this your Best decision ever”

 Become a Clinical Research Scientist

Clinical research scientists conduct research and clinical investigations of diseases and conditions to determine accurate diagnoses and effective treatments. They work in a variety of employment settings, including hospitals, universities and pharmaceutical labs. Safety precautions must be followed and protective gear used when dealing with potentially infectious samples.

Step 1: Earn a Bachelor's Degree in the Science Field

Although there are several different pathways to enter the clinical research profession, all prospective research scientists must possess a bachelor's degree in the biological sciences or a related field. Some institutions offer a degree specifically designed to prepare students to work in clinical research. This type of degree program includes courses in biochemistry, pharmacology, effective research techniques, scientific writing and data management. Regardless of major, undergraduate students intending to enter the field of clinical research should take courses in physics, mathematics, the biological sciences and chemistry.

Success Tip:

  • Participate in an internship. Clinical research scientist positions typically require experience. Completing an internship, which some programs may include as part of their bachelor's degree program curriculum, can provide this experience. Usually, during an internship, students are mentored by a qualified physician or scientific research specialist while they work on a research project.

Step 2: Complete an Advanced Degree Program in Science or Medicine

According to the U.S. Bureau of Labor Statistics (BLS), most clinical research scientist positions require either an advanced degree in the biological sciences or a medical degree. Graduate degree programs in biochemistry, cellular and molecular biology, microbiology or neuroscience often satisfy this requirement. However, some universities offer master's degree programs in clinical research. Students in these programs learn about research procedures, scholarly publication practices, biostatistics, professional ethics and clinical trial practices. Alternatively, obtaining a Medical Doctor (M.D.) or nursing degree may qualify individuals to work in the field.

Success Tip:

  • Consider completing a dual degree. The BLS states that many clinical research scientists choose to complete a dual degree program with majors in medicine and science. In fact, some job postings found in October 2012 required that candidates possess dual degrees. Students in these dual degree programs learn about medical practices and advanced research methodology. Possessing two graduate degrees may make students eligible for more job positions after graduation.

Step 3: Work as a Clinical Research Associate

The ACRP states that aspiring clinical research scientists typically begin their careers in entry-level positions, possibly as a clinical research associate. These associates typically assist research scientists in designing and administrating clinical trials. They also help evaluate gathered data and monitor the procedures to assure that the methodology complies with professional protocol.

Success Tip:

  • Earn a certificate. The ACRP currently offers three credentials to clinical research professionals: the Certified Clinical Research Associate, Certified Clinical Research Coordinator and Physician Investigator. Earning any of these certifications requires passing an exam. These certifications are recognized in the industry as indicating verifiable job skills and, therefore, may help individuals advance in their careers.

Step 4: Work as a Clinical Research Scientist

Clinical research scientists may work at universities, hospitals, pharmaceutical companies or for the federal government. These scientists typically perform analysis on cells, tissue and organs to identify bacteria and toxins with the goal of understanding the causes of diseases and being able to develop vaccines or medicines for treatment. However, some clinical research scientists may work directly with patients in health settings by administering clinical trial drugs and therapies, while others may instruct physicians, resident and technicians about medical laboratory procedures.
Research scientists have opportunities to advance to supervisory or project lead positions with enough experience and strong job performance. High-level managerial and administrative positions within their respective medical facilities may also be available with advanced experience and leadership acumen.
Environmental Science is a diverse field that offers those who study it multiple paths to challenging and rewarding careers in the future.
Whether it's an environmental scientist or specialist who works in a lab or a natural resource manager who looks after the distribution of the Earth's precious materials, a career in environmental science is for the environmentally-minded individual who wants to make a difference on our planet.
Being such a broad and generalized field, environmental science provides a plethora of interesting professional opportunities. Since education and concentrations possess such a strong influence over the type of job that you will be eligible for post-graduation, it's important to do research and select a career to work toward. It shouldn't be hard finding a career that combines your interests and passion for the environment and provides you with not just a secure job, but also personal fulfillment and enrichment.





Figure out the most popular careers
Our summary of the most popular careers within environmental science will get you kick started on figuring out which might be best for you. If your passion is not a top 5 career, do not worry! In general environmental science is a growing field and becoming more important for the planet. But, it would be responsible of you to research your passion to make sure the outlook is good for the career.
2.
Get a degree in an associated field
There are a number of options for an Environmental Science degree. Likewise, there are now more options for online degrees in Environmental Science. Some of the programs have specific concentrations associated with them but a degree in Environmental Science will more than likely at least allow you to get a foot in the door.
3.

The list of career options within Environmental Science goes far beyond our "Top 5 Most Popular Environmental Science Careers" list. Below are a few other careers - there are many options!

  • Agricultural Engineer
  • Anthropologist
  • Archaeologist
  • Bioinformatics
  • Climatologist
  • Ecologist
  • Entomologist
  • Geographer
  • Hydrologist
  • Marine Biologist
  • Meteorologist
  • Microbiologist
  • Molecular Biologist
  • Oceanographer
  • Paleontologist
  • Seismologist
  • Wildlife Biologist
  • Zoologist

Medical Writer- Clinical Research Organisation (bangalore & Gurgaon)

Kelly Services India Pvt. Ltd. hiring for Kelly Client
1 - 6 yrs
Bengaluru/Bangalore , Gurgaon

Job Description
    Undertakes project specific activities with minimal supervision from seniors at high quality and in defined timelines according to standard processes and operating procedures.
    Writing, editing and summarising clinical documents such as clinical study reports, narratives, clinical summaries or others with minimal supervision
    Systematically review or perform quality control checks of
     documents prepared by other Associates against pre-specified check-list and follow up independently till final submission
    Assist in mentoring and training of team members depending upon project requirement
    Participates in project specific meetings with client colleagues
    Performs detailed analyses on a planned and ad hoc basis, relating to the medical writing processes and their outputs

    Designation- Associate/Senior Associate- Medical Writing.

    Location- Bangalore & Gurgaon
    Company Profile:
Kelly Services India Pvt. Ltd.
Kelly Client
MNC-Clinical Research Organisation  

Healthcare and analytics @ Accenture
Accenture

- Job description

Job Requirement

-    Is a Subject matter expert for Health Admin and Care Management functions and hasa exposure to analytics
-    From Domain has exposure and knowledge of Health Payer Services
-    understanding of process requirements
-    Regulatory requirements
-    Leading practices
-    Exposure/good awareness of Health/Care Management and Pharmacy Benefits Managers Services 
-    Exposure / awareness of Provider Revenue Cycle Services appreciated
-    Should have worked in multiple areas of Health Payer/PBM Operations, Service Delivery, Analytics and Reporting etc.
-    Should have had exposure to fraud analytics etc

-    Has the ability to leverage industry and domain knowledge to drive delivery excellence (best practices, quality principles, best in class technology and tools, productivity, analytics)
-    Special focus on driving analytics, client business value, process benchmarking and productivity improvements across global portfolio
-    Is able to work with multiple stakeholders e.g. delivery leads, account management, clients and operational excellence teams
-    Has engaged directly with Clients (CXOs and Senior Executives levels preferred)
-    Has done solutioning/consulting
Responsibilities/Authorities

-    Act as Subject Matter Expert for Health Admin and Care Management offering (both Lines of Business preferable) for Accenture’s global Health Industry outsourcing portfolio.
-    Must bring in deep domain expertise, thought leadership, understanding of current & future trends of the insurance industry
-    Able to leverage domain to identify/recommend latest technology platforms to take
-    Insurance offering to the next generation in Outsourcing journey
-    Drive globally service excellence and client value through analytics, best practices, quality principles, best in class technology and tools, process and productivity benchmarking
-    Design, build, deploy and maint
- Basic qualifications

Job Description

Hi, 

We have walk in interview for Medical Writing on 30-June 

Job Role 
Draft Narratives
Perform 100% data-review and finalization of Narratives
Fill the defect tracker and track errors in every medical writing project
Coordinate a set of medical writing activities associated with a drug program therapy team
Review and QC all deliverables
Ensure that documents are approved and issued in accordance with timelines
Request data sources and attend client calls for medical writing deliverables kick-off meetings, review meetings and status updates

If  Interested please walk in below address or share resume with dipika.sharma@cognizant.com

30-June-2016
(Walk In)

9.30am 10.30am

2nd Floor,Building No 9,Mindspace SEZ,
Thane-Belapur Road, Airoli

Contact Person :
Dipika SharmaCompany Profile
Cognizant (NASDAQ: CTSH) is a leading provider of information technology, consulting, and business process outsourcing services, dedicated to helping the world's leading companies build stronger businesses. Headquartered in Teaneck, New Jersey (U.S.), Cognizant combines a passion for client satisfaction, technology innovation, deep industry and business process expertise, and a global, collaborative workforce that embodies the future of work. With over 100 development and delivery centers worldwide and approximately 221,700 employees as of December 31, 2015, Cognizant is a member of the NASDAQ-100, the S&P 500, the Forbes Global 2000, and the Fortune 500 and is ranked among the top performing and fastest growing companies in the world. Visit us online at www.cognizant.com or follow us on Twitter: Cognizant.

Job Opening for Zydus Cadila- API Ahmedabad Location

1 - 6 YearsAhmedabad

Job Description

Officer to Deputy Manager Vacancies:

Open Vacancy: 2

ADL : M.Sc./Ph.D with 2 - 8 years relevant experience and exposure to method development, method validation, handling HPLC, UPLC, LC-MS, XRD, GC, calibration & trouble shooting. 

DQA: 
B. Sc./M. Sc. / B. Pharm/M.Pharm with 1 to 6 years experience and exposure to Preparing and Reviewing of documents related to R&D.Should also Ensure proper maintenance of central documentation.


Open Vacancy: 2

Quality Control:
 
B. Sc./M. Sc. / B. Pharm with 2 to 8 years hands on experience of HPLC, GC, dissolution apparatus, and UV-visible spectrometer. Should also have knowledge of weight analysis, stability studies for parenteral preparations and solid dosage forms. Knowledge of LIMS would be preferable.

Company Profile

Zydus Cadila is one of India's leading healthcare companies and a global healthcare provider with strengths all along the pharmaceutical value chain. The group's state-of-the-art manufacturing infrastructure is spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim and the R &D Centres are spread across Ahmedabad, Baroda and Mumbai (Thane)

Manager -logistics Cold \chain Management (12-15 Years)


10 - 15 YearsBengaluru/Bangalore

Job Description

1. Planning and executing temperature controlled shipment operations.
2. Co- ordination with M arketing, SCM-Planning, Production & QA.
3. Planning of pre shipment dispatch requirements, co-ordinate with the concerned departments for compliance.
4. Ensure timely submission of post-dispatch documents to bank for the payment clearance.
5. Ensure timely submission of post-dispatch documents to respective functions for the claim of export incentives.
6. Periodical MIS related to the function.
7. Evaluating alternate service providers and ensuring appropriate service level agreements
8. Identify the operational bottlenecks in the system and action plan for improvement.
9. Co-ordinate with SAP team for system improvements.
10. Handling customer complaints & workout the solution with CAPA.
11. Compliance of Good Distribution Practices
12. To ensure logistics process and operation are enabled for 100%OTIF
without any delay, without temp excursion (for cold) ,without any damage & loss
13. To ensure allocation of available resources and to make optimal strategic choices to help the organization reach the goal.
14. To operationalizes quality standards and develop new processes or improve existing processes to ensure compliance with operational excellence
15. To set clearly defined goals and performance parameters for each team member
16. To ensure regular reviews of the progress against the set objectives jointly with the team member
17. cold chain Management.Company Profile
Biocon is an integrated biotechnology enterprise focused on the development of biopharmaceuticals. With successful initiatives in drug discovery and development, bioprocessing, manufacturing and global marketing, Biocon delivers products and solutions to partners and customers in over 75 countries. Biocon has the defining science, world class capabilities and a focused vision to deliver the promise of innovative and affordable medicine to a waiting world. Today, Biocon together with group companies employs more than 5000 employees with approxmimately Rs 2500 crore turnover and is expected to grow further during the current financial year .

 Trainee - Clinical Trial Co-ordinator

Dr Lal Path Labs (Pvt) Ltd
0 - 1 yrs
Delhi

Job Description
    Looking for a fresh candidate for Clinical Trials Co-ordinator
Company Profile:
Dr Lal Path Labs (Pvt) Ltd
LPL offers access to diagnostic healthcare services in India through our nationwide network of clinical laboratories

Medical Coding Job for Non Life Science Graduate Along with Training


Synthesis healthcare Services LLP
0 - 2 yrs
Chennai
Walkin Interview
29th June - 15th July 9 AM

Job Description
    Greetings from Synthesis Healthcare Services LLP!!
    Its our warm pleasure to introduce about ourselves.
    We are pioneer in US Healthcare services. The offshore services include End to
    End services in US Healthcare segment like Coding, Billing, Claims Adjudication and
    Medical coding Training. The management team has more than 400 years of
    aggregate experience in US Healthcare services. Synthesis Healthcare Services is
    a leader in the US Healthcare space in providing Medical Coding, Coding Audit, and
    Billing Audit services. Since inception Synthesis Healthcare has been providing
    value added services in both Payer and Provider business. 
    We are conducting Medical Coding Course - paid batch May 2016
    Salient Features of the course
    Medical Coding job for non life science graduate
    Exposure to coding Practice
    Intensive Classroom traininig
    Job Available for successful canddiates*
    ICD & CPT
    Eligibility Criteria
    Any DegreeCompany Profile:
Synthesis healthcare Services LLP
Nittany is pioneer in Art Work, Digitizing, Embroidery, Software / Web Development and Order Entry Processing serving various customers in US, UK and Canadian regions for over 16 years.

Walkin Interview
29th June - 15th July 9 AM 

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