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Tuesday 31 May 2016
| UnitedHealth Group |
| Designation | Medical Coding Analyst |
| Job Description | Details of Responsibilities / Purpose of Job: Research and resolution of coding projects as assigned. 1. Perform ongoing analysis of medical record charts for the appropriate coding compliance. 2. Coder is responsible for meeting daily production goal of 6 charts per hour. 3. Coder is responsible for meeting quality coding goal of averaging 95% accuracy rate on a monthly basis. 4. Attend conference calls as necessary to provideSpecific Measurements of Performance:- Quality audits are conducted monthly on 10% of all charts coded per coder. - Production is monitored weekly/ monthly to ensure coders are being productive. Apply now |
Job Description
Greetings from ELICO!!!
We have an urgent requirement for ED/EM Coding
Coding Certification Must.
Location Hyderabad
Experience- > 1 year in ED
Operation Skill
> Charts audit and feedback to coders on daily basis
> Day to day management of quality and related escalation.
> Performance and feedback Management for coders.
> Quality team Representation for client management call.
> Verifying the core system to control the workflow including data management.
> work-plan management
> Operational Crisis, BCP, Backlog planning and management
> Efficient communication skill to deal with USA based client
Training Skill
> Internal Team training management and GAP fill on weekly basis for internal training requirement.
> Practical Case study discussion, improving, performance and gap analysis and management.
> Internal and Client related Training Knowledge management.
> client level SOP review and update on regular basis
Quality Management
> Day to day QC management.
> Acuity Level Analysis.
> QA report analysis and Management.
> Focus and compliance audit for sample charts.
> Special client related/requested audit and reporting.
> Provider specific and documentation specific audit planning and management.
> Feedback and continuiong education for the coders on daily basis.
We have an urgent requirement for ED/EM Coding
Coding Certification Must.
Location Hyderabad
Experience- > 1 year in ED
Operation Skill
> Charts audit and feedback to coders on daily basis
> Day to day management of quality and related escalation.
> Performance and feedback Management for coders.
> Quality team Representation for client management call.
> Verifying the core system to control the workflow including data management.
> work-plan management
> Operational Crisis, BCP, Backlog planning and management
> Efficient communication skill to deal with USA based client
Training Skill
> Internal Team training management and GAP fill on weekly basis for internal training requirement.
> Practical Case study discussion, improving, performance and gap analysis and management.
> Internal and Client related Training Knowledge management.
> client level SOP review and update on regular basis
Quality Management
> Day to day QC management.
> Acuity Level Analysis.
> QA report analysis and Management.
> Focus and compliance audit for sample charts.
> Special client related/requested audit and reporting.
> Provider specific and documentation specific audit planning and management.
> Feedback and continuiong education for the coders on daily basis.
Please contact on : 8978447766/ 8008804661 / (040)44451205
Company Profile
ELICO Healthcare Services Ltd (EHS) was established as a wholly owned subsidiary of ELICO Ltd. The Company provides remote processing services to Medical Billing Companies. Ambulance Billing Companies. Surgery Centers, Nursing Homes and Hospitals based in USA, UK & Middle East.
- - Perform Site Identification and conduct feasibility studies.
- Perform Site Selection Visit, Site Initiation visits in accordance with the protocol and other applicable regulatory guidelines including local regulatory guidelines.
- Perform Site Monitoring Visit, Site Close-out visits in accordance with the protocol and other applicable regulatory guidelines including local regulatory guidelines.
- Keep a close association with site for Patient Recruitment, patient follow-up and protocol related activities.
- Act as a communication link between Sponsor and site.
- Attend Investigator's meeting.
- Training of Investigators on Protocol and other applicable regulatory guidelines including local regulatory guidelines.
- CRF retrieval as per the project instructions.
Company Profile:
Multiple Job Opportunities for experienced Clinical Research Professionals having knowledge and experience in ClinicalResearch/Trial Field.
Required Experience - 2 to 3.5 years
JOB DESCRIPTION/JOB RESPONSIBILITIES
PURPOSE
PURPOSE
Provide project related assistance for assigned complex project(s), sites and project teams. Ensure all work is conducted in accordance with SOPs, policies and practices, good clinical practices and applicable regulatory requirements and meets quality and timeline metrics.
RESPONSIBILITIES
Perform complex processes and tasks that eventually result in high quality deliverables that are completed according to service level agreements (SLAs) and within project timelines
Establish and maintain effective project/ site communications
Create and maintain relevant project documents Ensure accurate completion and maintenance of internal systems, databases, tracking tools, timelines and project plans with project specific information
Participate in document management (creation, review, maintenance, storage, as applicable)
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Good knowledge of applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws,
regulations and guidelines
Strong written and verbal communication skills including good command of English language
Results and detail-oriented approach to work delivery and output
Good problem solving skills
Good planning, time management and prioritization skills
Attention to detail and accuracy in work
Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel
and PowerPoint
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Proven ability to work on multiple projects balancing competing priorities
Ability to coach/ mentor junior colleagues
REQUIRED SKILLS AND ABILITIES
Excellent verbal and written communication skills
Willing to work in Shifts (6AM- 2:30 PM & 2PM-10:30 PM)
Address:
12th Floor, G Corp Tech Park,
Next to Hypercity Mall,
Ghodbunder Rd, Thane,
Maharashtra 400601
Next to Hypercity Mall,
Ghodbunder Rd, Thane,
Maharashtra 400601
Company Profile:
Contributes directly to the company's revenue by performing programming and validation of client deliverables in Data Management and Biostatistics. Successful completion of assigned tasks increases the likelihood of repeat business from the client and on-going success in acquisition of new business.
Functions and Responsibilities:
Independently create, execute, maintain, and validate programs that transfer data across multiple data management systems or operating systems, combine data from a variety of sources and structures, generate and store summary data from a variety of sources, generate reports or combine multiple databases.
Independently create, execute, maintain, and validate programs that generate listings, tables and figures using SAS, or other appropriate languages.
Perform other programming tasks as necessary to support Clinical Data Management and Biostatistics.
Assess and ensure the validity of all program output.
Serve as a project lead and oversee work of other programmers on team.
Responsible for clearly documenting all work; managing assignments to meet timelines and producing high quality deliverables.
Function as a contributing member of a multi-disciplined team.
Actively seek information to gain good understanding of the role of the programmer in the overall process.
Increase knowledge base and professional skills in areas including programming, technology and techniques, clinical trials, and the pharmaceutical industry.
Provide general infrastructure support to the Biostatistics Department. Examples include presentation / teaching at Department meetings, contributing to other general department documents and policies, or assisting with Biostatistics web page content.
Understand and follow departments working practice documents and SOPs, and contribute to their development as needed.
Understand and follow appropriate corporate SOPs.
Functions and Responsibilities:
Independently create, execute, maintain, and validate programs that transfer data across multiple data management systems or operating systems, combine data from a variety of sources and structures, generate and store summary data from a variety of sources, generate reports or combine multiple databases.
Independently create, execute, maintain, and validate programs that generate listings, tables and figures using SAS, or other appropriate languages.
Perform other programming tasks as necessary to support Clinical Data Management and Biostatistics.
Assess and ensure the validity of all program output.
Serve as a project lead and oversee work of other programmers on team.
Responsible for clearly documenting all work; managing assignments to meet timelines and producing high quality deliverables.
Function as a contributing member of a multi-disciplined team.
Actively seek information to gain good understanding of the role of the programmer in the overall process.
Increase knowledge base and professional skills in areas including programming, technology and techniques, clinical trials, and the pharmaceutical industry.
Provide general infrastructure support to the Biostatistics Department. Examples include presentation / teaching at Department meetings, contributing to other general department documents and policies, or assisting with Biostatistics web page content.
Understand and follow departments working practice documents and SOPs, and contribute to their development as needed.
Understand and follow appropriate corporate SOPs.
Company Profile
PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 46 countries and more than 15,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help clients and partners bend the cost and time curve of drug development to deliver life-changing therapies that improve health. For more information, visit www.ppdi.com.
Job Description
PURPOSE OF THE JOB
The position manages a group of highly experienced DSU, Case Processing and Medical Review team in the PV project. The profile is the primary interface with the client team.
MAIN ACCOUNTABILITIES
Accountable for performance, consistency, and quality of the deliverables.
Ensure team members are trained and mentored appropriately.
Ensure the completeness and validity of cases submitted to the client.
Ensure product delivery to client timeline and quality expectations.
Resolve data issues with the Client Team.
Balance workload within a team of DSU, CP & MR programmers and ensure timelines are met.
Implement measures to ensure corrective actions are taken.
Resolve any issues identified by the team.
Accountable for providing updates to the team any changes in the way in which work is performed. Ensure efficiency of operations.
Update the employee ware house hosting the individual productivity and employee leave details within the defined time frames.
Provide feedback to QC roles for quality and efficiency improvement and ensure necessary corrective measures are taken.
Production ready assessment support new employees in their Production work.
Organize mentoring for new employees as and when required.
Recruit and hire the right skills
Identify opportunities for continual improvement.
Implement best practices for quality deliverable to client.
People management and mentoring team members to ramp up and deliver as per client requirements.
Ensuring customer satisfaction on project deliverables.
Ability to manage a team size of over 80
DIMENSIONS
Will oversee PV operations for all cases and manage a group of all DSU, CP & MR.
Track and publish projects and metrics
Conduct performance review / assessments of DSU, CP & MR.
Engage in frequent communication with on-shore and of
The position manages a group of highly experienced DSU, Case Processing and Medical Review team in the PV project. The profile is the primary interface with the client team.
MAIN ACCOUNTABILITIES
Accountable for performance, consistency, and quality of the deliverables.
Ensure team members are trained and mentored appropriately.
Ensure the completeness and validity of cases submitted to the client.
Ensure product delivery to client timeline and quality expectations.
Resolve data issues with the Client Team.
Balance workload within a team of DSU, CP & MR programmers and ensure timelines are met.
Implement measures to ensure corrective actions are taken.
Resolve any issues identified by the team.
Accountable for providing updates to the team any changes in the way in which work is performed. Ensure efficiency of operations.
Update the employee ware house hosting the individual productivity and employee leave details within the defined time frames.
Provide feedback to QC roles for quality and efficiency improvement and ensure necessary corrective measures are taken.
Production ready assessment support new employees in their Production work.
Organize mentoring for new employees as and when required.
Recruit and hire the right skills
Identify opportunities for continual improvement.
Implement best practices for quality deliverable to client.
People management and mentoring team members to ramp up and deliver as per client requirements.
Ensuring customer satisfaction on project deliverables.
Ability to manage a team size of over 80
DIMENSIONS
Will oversee PV operations for all cases and manage a group of all DSU, CP & MR.
Track and publish projects and metrics
Conduct performance review / assessments of DSU, CP & MR.
Engage in frequent communication with on-shore and of
Company Profile
Accenture is a leading global professional services company, providing a broad range of services and solutions in strategy, consulting, digital, technology and operations. Combining unmatched experience and specialized skills across more than 40 industries and all business functionsunderpinned by the worlds largest delivery networkAccenture works at the intersection of business and technology to help clients improve their performance and create sustainable value for their stakeholders. With approximately 373,000 people serving clients in more than 120 countries, Accenture drives innovation to improve the way the world works and lives
Syngene Hiring Multiple Executive / Sr.executive / Jr.manager / Asst.mgr - Downstream Manufacturing
Job Description
- Expertise in purification of recombinant proteins and monoclonal antibodies with mammalian cell culture system
- Experience in purification of monoclonal antibodies in large scale operation
- Exposure to purification of wide variety of proteins ( novel and biosimilars)
- Exposure to develop the strategy for large scale downstream process
- Experience on Scale up , technology transfer, and purification operation at large scale
- Experience in handling on downstream process equipments such as continuous centrifuge, depth filtration ,chromatography system, column chromatography , column packing and filtration skids
- Experience in trouble shooting operation in protein purification process
- Strong knowledge of cGMP operation, quality guidelines and standards with ability to interpret and apply them.
- Experience and technical knowledge in biologics drug product operations
- Experience in writing GMP documents such as batch manufacturing records, tech transfer document, batch reports, batch trending and analysis, operating procedure, deviation reports and other related documents.
- Proven ability to rapidly adapt to changing environment and circumstances requiring flexibility
- Proficiency with use of global systems of documentation & enterprise management system (e.g. SAP)
Company Profile
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. The state-of-the-art research facilities have been qualified by various pharmaceutical majors & regulatory agencies and has received various certifications including ISO 9001: 2008, ISO 14001:2004, OHSAS 18001:2007, GLP and AAALAC.
Over the past 16 years, Syngene has successfully partnered with leading pharmaceutical companies, large biotech companies, crop protection companies and cosmetics companies. Syngene together with Bristol-Myers Squibb has set up a dedicated research facility in Bangalore to help advance Bristol-Myers Squibb's work in discovery and early drug development.
To advance its programs and expand its capabilities, Syngene is looking to recruit outstanding scientific talents.
So come and join us in our journey of scientific innovation.
For further details, please visit www.syngeneintl.com.
Over the past 16 years, Syngene has successfully partnered with leading pharmaceutical companies, large biotech companies, crop protection companies and cosmetics companies. Syngene together with Bristol-Myers Squibb has set up a dedicated research facility in Bangalore to help advance Bristol-Myers Squibb's work in discovery and early drug development.
To advance its programs and expand its capabilities, Syngene is looking to recruit outstanding scientific talents.
So come and join us in our journey of scientific innovation.
For further details, please visit www.syngeneintl.com.
- Job Title Associate Medical Writer
PURPOSE
Assists senior medical writing staff in the preparation of study reports, submissions, or other documents for either internal Quintiles customers or external clients, for investigational drugs, biologicals, or medical devices. Participates in project teams and may lead specific straightforward or small tasks, consulting senior staff as necessary.
RESPONSIBILITIES
Supports Medical Writing senior staff in managing client requests. Examples include but are not limited to the following:writing patient narratives, straightforward bioanalytical study data reports, checking document edits, checking documents for consistency, adapting generic document shells to project specifications, assisting with document compilation, and entering numbers into in-text tables. May also draft text for simple documents, reports or sections of documents or reports, with guidance of senior staff.
Identifies project needs, tracks project timelines and implements client requests, with senior review.
Interacts with internal clients. May have some external interactions, mostly directed by senior staff.
Takes responsibility for managing day-to-day workload for assigned tasks, in collaboration with senior staff.
Keeps abreast of current data, trends, medical and/or technical writing/regulatory knowledge, developments and advances in area of drug development/medical and/or technical writing.
Complies with Company SOPs and participates in the implementation of new SOPs.
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Excellent standard of written English, and ability to communicate fluently and effectively in English, both in writing and verbally.
Ability to work on several projects at once while balancing multiple and overlapping timelines.
Ability to assess workload and suggest prioritization to senior staff.
Demonstrated abilities in collaboration with others and independent thought.
Knowledge of regulations relevant to medical/technical writing, such as Good Laboratory Practices (GLP) and other relevant regulatory agencies (e.g. OECD, MHLW).
Careful attention to detail and accuracy.
Must be computer literate.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Company Profile:
Monday 30 May 2016
Opportunity to work as Stability Integrator @ Johnson & Johnson
Job Description
Requisition ID: 0000155S
Janssen Supply Group, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for a Stability Integration Specialist in Raritan, NJ, Titusville, NJ, Beerse, BE, Guaynabo, PR, or Higi, India.
At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found.
Janssen Supply Group, LLC is a global organization responsible for producing and supplying medicines to markets around the world. With quality as its primary focus, this group collaborates with Research & Development and Commercial partners to deliver life-changing solutions for patients in need.
We are Janssen. Our mission drives us. Our patients inspire us. We collaborate with the world for the health of everyone in it.
Global Stability Operations is a department within the Janssen supply chain, responsible for the stability management of pharmaceutical products and active pharmaceutical ingredients manufactured in the different manufacturing sites worldwide and for the site-to-site analytical method transfers within Janssen Supply Chain (JSC).
The Stability Integration Specialist will:
Be responsible for Stability Management of Drug Substance/Drug Products and site-to-site Analytical Method Transfers within JSC.
Handle Stability and Analytical Transfer Management of a portfolio of products.
Be the first point of contact for stability and transfer related issues and lead for escalating stability OOT/OOS (out of tolerance/out of scope).
Trend and profile product behavior.
Support and coordinate investigations.
Perform Scientific and Quality evaluation of generated results.
Draw up conclusions on shelf life/ retest period, storage conditions and instructions, shipment excursions and method transfer status.
Assure resources are planned (e.g., stability storage conditions and space, equipment, reagents, people, skills, etc.).
Coordinate Safety Health & Environmental (SHE) assessments of new chemicals and reagents for the stability testing labs.
Assess readiness of the stability group for New Product Introductions (NPI).
Participate in projects as stability expert.
Ensure compliance with all relevant regulations, guidance, compendial requirements for stability studies, analytical methods and specification.
Qualifications
A minimum of a Bachelor’s degree or equivalent degree is required
A degree focused in Science, Pharmacy or Industrial Engineering is preferred
A minimum of 4 years of relevant experience is required
Strong knowledge of related domestic and international Stability guidelines for the Pharmaceutical/OTC business is required
Experience facilitating or contributing to method transfers is required
Advanced computer skills and experience with MS software applications (Word & Excel) are required
Experience with Minitab, LIMS and Trackwise are preferred
Good knowledge of statistical data analysis is required
Project management experience and related certifications (PMP, FPx, etc.) are preferred
Experience working in a large enterprise, global environment is preferred.
This position will be based in Raritan, NJ, Titusville, NJ, Beerse, BE, Guaynabo, PR, or Higi, India and may require up to 5% travel.
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