No of position: 1

Job Location: Noida

Required Experience and Skills

• 4+ years’ experience in PV domain
• Preferrable experience in ARISg/Argus safety database technical knowledge
• Ensure and maintain quality metrics 95%+
• Handle server/service/scheduler related issues as per client SOP
• Understand and develop SQL/PL SQL scripts/procedures
• Build understanding of user acceptance testing (UAT) and support in UAT executions
• Lead problem solving sessions
• Provide timely resolution of service requests
• Perform safety systems configuration

Skills and Competencies

• Must have good written & oral communication skills.
• Timely attend and respond to assigned tasks as per business need
• Possesses good analytical and reasoning Skills.

Education

• B.E /B. Tech/ MCA or any related bachelor’s degree

Job Location: Pan India

Required Experience and Skills

• 5+ years’ experience in PV domain
• Experience in authoring OQ, PQ, UAT Scripts
• Author client owned user requirements
• Review ARISg configuration requirements
• Participate in root cause analysis of testing issues
• Draft client business informal test scenarios and support execution of the business testing
• Familiar with Software Development Lifecycle (SDLC)

 Skills and Competencies

• Possesses good analytical and reasoning Skills.
• Knowledge of Pharmacovigilance domain and Drug Safety Systems
• Must have good written & oral communication skills.

Education

• B.E /B. Tech/ MCA or any related bachelor’s degree

No of position: 1

Job Location: Noida

Required Experience and Skills

• 5+ Years’ experience in BO/Cognos Reports and PV domain
• Experience in developing and implementing reports based on client specifications
• Experience in deploying BO, creating Universe and setup of Framework Model in Cognos
• Good knowledge in creating Webi, Desktop reports in BO and Report studio, Query studio in Cognos
• Understanding business requirements and documentation
• Good knowledge in Central Management server of BO and Framework Manager in Cognos
• Experienced in creating Database/Data source and customize Reports.
• Experienced in RDMS and writing SQL/PLSQL.
• Good with Analytics, Troubleshooting skill, dashboards

Skills and Competencies

• Possesses good analytical and reasoning skills.
• Must have Knowledge of Pharmacovigilance domain and Drug Safety Systems
• Must have good written & oral communication skills.

Education

• BE /B. Tech/ MCA or any related bachelor’s degree.

No of positions: 6

• 2 positions – Software Engineer (2+ years of experience)
• 2 positions – Sr. Software Engineer (4 + years of experience)
• 2 positions – Software Architect (8+ years of experience)

Job Location: Noida (Work from office)

Required Experience and Skills

• 2 to 8+ years of experience in .Net technology.
• Proficient in C#, Linq, jQuery, MVC, Entity framework, web/window services, ADO.NET, NoSQL DB.
• Strong understanding of object-oriented programming
• Expertise with Oracle (or SQL server)
• Experience with JavaScript.
• Proficient understanding of code versioning tools such as Git, SVN.
• Understanding of Agile methodologies
• Lead problem solving sessions
• Provide timely resolution of service requests

Skills and Competencies

• Excellent troubleshooting and communication skills
• Timely attend and respond to assigned tasks as per business need
• Possesses good analytical and reasoning skills.

Education

• B. Tech/ BCA/MCA or any related bachelor’s degree

No of Position: 1

Job Location: Pan India

Experience: 2-4 Years

Required Experience and Skills

• Hands on experience on MedDRA and WHO Drug dictionaries
• Experience in Core clinical coding using both MedDRA and WHODD will be preferred.
• Be knowledgeable of MedDRA points to consider and WHODD best practices.
• Be knowledge of industry best practices in medical coding
• Is able to read and understand the coding conventions applicable to each coding project
• Knowledgeable in multiple coding tools shall gain add-on benefit.
• Is able to conduct impact analysis of coded data against new version of the dictionary.
• Perform medical coding activities maintaining optimal communication with stakeholders for coding query resolution.
• Maintain appropriate training requirements.
• Should have sound knowledge of Clinical data management workflow.

Skills and Competencies

• Must have good written & oral communication skills.
• Timely attend and respond to assigned tasks as per business need.
• Possesses good analytical and reasoning skills.

Education

• B. Pharm, M. Pharm or diploma in related field.

No. of position: 1

Job Location: USA(NY/NJ). The candidate will be working from Prudentia’s Jersey City office

In 2017, Prudentia launched MedCodr (www.medcodr.com) which quickly became a leading application for coding adverse event terms and drug products to standard dictionaries such as MedDRA and WHO DD.  Prudentia also launched a service to perform medical coding on behalf of our clients.  Your job is to set the direction for MedCodr, establish and run the governance structure, market MedCodr, lead pricing and contracting discussions for MedCodr, and serve as the main point of contact for MedCodr at our clients.  The ideal candidate has a strong coding background, experience as a product manager, and a manager who can lead a team through releases of the system.

Responsibilities

• Business development for Medcodr and medical coding services
• Maintaining client relationships for Medcodr and coding services
• Developing, maintaining, and directing the roadmap for Medcodr
• Enhancing and running the governance structure of Medcodr
• Understanding and directing the functionality of Medcodr
• Establishing and executing the end-user training for Medcodr
• Promoting, directing, and ensuring the quality of Prudentia’s medical coding service
• Overall support of Prudentia’s sales, recruiting, and internal practice development as directed.

Skills and Competencies

• 5+ years of experience as a medical coding specialist
• Experience in product development a plus
• Experience in business development or managing clients a plus
• Experience as a project manager in clinical development, regulatory affairs, or pharmacovigilance a plus
• Knowledge of MedDRA and WHODrug dictionariesare pluses
• PV experience as a safety specialist is a plus

Education

• Healthcare professional or
• Master/Bachelor ‘s degree in computer science, management information systems

Job Location: USA(NY/NJ). The candidate will be working from Prudentia’s Jersey City office, remotely from your home office, and at client locations.

Description

As a business intelligence consultant, you will be responsible for designing and implementing business intelligence solutions for our clients.  You will design ETLs from the client’s transactional database or replica.  You will design the data warehouse as well as the denormalized business intelligence layer.  You will gather the requirements for reports and implement the reports.  Your knowledge of PV together with your deep understanding of BI technologies will enable you to develop reporting solutions to meet our clients’ data information needs.

Required Experience and Skills

• 5+ years’ experience in one or more business intelligence platforms such as BO, Cognos, OBIEE, Tableau, Qlik Sense, Power BI, SAS, and Spotfire in the PV domain
• 5+ years’ experience with developing queries and procedures in relational databases such as Oracle, Postgres, SQL Server, MySQL
• 2+ years of experience with multi-dimensional/NOSQL databases such as Hbase, MongoDB, Apache Cassandra
• Experience with using extract, transformation, and load (ETL) tools such as Infomatica, IBM Datastage, SAP BODI, Oracle Data Integrator, Ab Initio
• Experience with developing ETL tools for both full and incremental loads
• Experience with designing business intelligence solutions from tools to request reports, to query building tools, to report painters, to scheduled reports, to data set retention, to drill-down reports.
• Experience in deploying BO, creating universe
• Experience in setup of Cognos Framework Model
• Experience in using BO’s Webi and Desktop reports
• Experience in using Cognos Report studio and Query studio
• Experience in using BO’s Central Management server
• Experience in using Cogno’s Framework Manager
• Good with Analytics, troubleshooting skill, dashboards

Skills and Competencies

• Possesses good analytical and reasoning Skills.
• Knowledge of Pharmacovigilance domain and Drug Safety Systems

• Must have good written & oral communication skills.

Education

• Advanced degree in computer science, life sciences, or engineering

Job Location: USA(NY/NJ). The candidate will be working from Prudentia’s Jersey City office, remotely from your home office, and at client locations.

Description

As a business analyst you will contribute to and lead the analysis, business process, requirements, training, test approach, and deployment for safety database (Aris Global’s LSMV, Oracle Argus, Veeva Vault Safety) upgrades, data migrations, Prudentia applications (PV Trend, NEOS, MedCodr), data mart design, and business intelligence integration.  You will also conduct inspection readiness assessments, safety organization design, PV business processor and safety database hosting selection.  As your career develops, you will progress as a project manager and lead specific work streams or the entire program.

As a business analyst you will also help sell our services by participating in proposals, reviewing master service agreements, authoring statements of work and change controls.  You will also assist with marketing campaigns and recruiting staff.

Required Experience and Skills

• 5+ years of experience as Business Analyst.
  • Responsible for scoping, planning, developing business process and supporting the implementation, requirements gathering and user acceptance testing.
  • Experience in system implementation or upgrades, data migration, custom reporting, and system integration
• Support project planning by defining required tasks and effort estimate.
• Lead/facilitate internal and/or client team workshops and meetings.
• Author business process documents such as SOPs, Work Instructions, process maps, and training materials
• Conduct training on business process and system functionality.
• Author system requirements such as User/Functional Requirements Specification
• Support end-to-end validation for a project by developing test scenarios, authoring, and executing test scripts.
• Conduct impact assessments against business process and corresponding systems for change requests.
• Review project deliverables for adherence to documentation standards
• Compare solutions and develop business case for the appropriate solution.
• Impart trainings to new hires, colleagues, and peers.

Skills and Competencies

• Pharmacovigilance and drug safety system experience
• Experience implementing clinical, regulatory, or PV solutions
• Strong problem-solving skills to identify root cause and propose simple solutions to complex problems
• Strong soft skills typically required as a business analyst.
• Demonstrates leadership in assignments and is able to engage a team towards ambitious goals.
• Proficient in using Microsoft application such as PowerPoint, MS Excel (spreadsheets, charts, pivot tables), MS Word, MS Visio, and MS Project.
• Proficient in using SharePoint applications such as “lists” for implementing trackers and RAID logs.

Education

• Advanced degree in computer science, life sciences, or engineering

Job Location: USA(NY/NJ). The candidate will be working from Prudentia’s Jersey City office, remotely from your home office, and at client locations.

Description

As a project manager you will sell, lead, and implement projects related to safety database (Aris Global’s LSMV, Oracle Argus, Veeva Vault Safety) upgrades, data migrations, Prudentia applications (PV Trend, NEOS, MedCodr), data mart design, business intelligence integration.  You will also conduct inspection readiness assessments, safety organization design, PV business processor and safety database hosting selection.  You may lead specific work streams or the entire program.  You will establish the program management office (PMO) with project plans, developing scorecards, facilitating status meetings and governance meeting, establishing and monitoring project trackers for issues, actions, risks, and questions, and developing communication plans.  You serve as the overall leader of projects providing administrative and subject matter direction to clients and Prudentia staff.

As a project manager you will also help sell our services by participating in proposals, reviewing master service agreements, authoring statements of work and change controls.  You will also assist with marketing campaigns and recruiting staff.

Responsibilities

• Serve as the manager for process and system implementations
• Assess the work effort and approach for the solution
• Drive the design of the solution
• Lead the planning and process workshops
• Establish project management office (PMO) and develop appropriate artifacts such as project plan, scorecards, status reports, communication plans, issue / action / risk / question tracker
• Lead gap assessments
• Direct, author, and review user and functional requirements
• Direct, author, and review validation plans,
• Direct, author, and review other validation artifacts such as OQ and PQ scripts, risk assessments, validation summaries.
• Design and run hyper-care support
• Assist with developing proposals and marketing materials
• Interview new candidates
• Mentor Prudentia resources

 Skills and Competencies

• 10+ years of experience with implementing safety databases such as Argus, ARISg, LSMV, or Veeva across various roles
• 5+ years of experience as a business analyst or a PM preferably within PV
• 2+ years of experience supporting or leading a PMO
• 2+ years authoring or reviewing validation artifacts
• Experience with supporting a data migration is a plus
• PV experience as a safety specialist is a plus

Education

• Bachelor ‘s degree in computer science, math, pharmacy. Masters preferred.