Job Description:

Review and analyze existing system structures to provide solutions to enhance and improve system. Work closely with system analysts to understand users system requirements, map process flow, design the processing steps, and analyze new systems.  Develop data migration tools and processes for new systems.  Setup test environment and test data for a timely and exhaustive project testing so that bugs and errors can be eliminated from the system. Participate in technical collaboration meetings, and provide the project management team with periodical reviews on implementation status as well as weekly reports on task plan for custom software implementations.  Provide the end users with system software supports and user trainings. Must be able to travel temporarily to client sites throughout the U.S.

Minimum Qualification Required:

Master or foreign equivalent in Computer Science, Computer Application, Computer Engineering, Computer Information System, Electronic Engineering, Electrical Engineering, any Engineering field or related field. In the alternative, will accept Bachelor or foreign equivalent plus five years of progressive experience in job offered or related work.

Job Description:

Assist in analyzing existing business procedures and practices to make recommendations to management and client to introduce more effective information technology business process and methods of operations. Assist in evaluating business functional requirements and organizational systems; perform data gathering, gap analysis and review, present recommendations, design and development of implementation processes, as well as documentation of the same. Assist in formulation and defining systems scope and objectives based on both business needs and industry requirements; in implementing design changes and research on management tools, models and methodology to devise most efficient methods of operations. Must be able to travel temporarily to client sites throughout the U.S.

Minimum Qualification Required:

Bachelors or foreign equivalent in Business Administration, Management Studies, Commerce, Finance, Management Info Sys or any related field.

Job Description:

Assist in reviewing and analyzing existing system structures to provide solutions to enhance and improve system. Work closely with system analysts to understand user’s system requirements, map steps, and analyze new systems. Assist in developing data migration tools and processes for new systems. Assist in setting up test environment and test data for a timely and exhaustive project testing eliminated from the system. Provide end users with system software supports and user trainings. Must be able to travel temporarily to client sites throughout the U.S.

Minimum Qualification Required:

Bachelors in Computer Science, Computer Application, Computer Engineering, Computer Information System, Electronic Engineering, Electrical Engineering, any Engineering field or related field

Job Description:

Conduct review and design the registration of clinical studies. Monitor quality of research and responsible

For Data collection and documentation. Manage the Trial Master File (TMF) ensuring all essential documents are tracked and filed in accordance with ICH/GCP guidelines. Monitor the clinical trial progress ensuring that it is recorded, conducted and reported in accordance with SOPs, protocol, GXP/ ICH and FDA 21 CFR and the relevant regulatory requirements. Responsible for site monitoring, site management, site administration and registry management for clinical studies according to GXP (GCP) and ICH Guidelines. Prepare, collect and review all essential documents throughout the study lifecycle. Provide training, administer protocol and ensure understanding of appropriate SOPs, ICH-GCP guidelines to assigned site. Responsible for preparation, completion and auditing of Informed Consent Forms. Responsible for gathering business requirement for development of Medscribe Electronic Medical Record System (EMR). Participated in drafting functional requirement and design specification for Medscribe Electronic Medical Record software. Responsible for Regression, Smoke, Functional, Blackbox and UAT testing to make sure the business requirement are fulfilled. Performed Risk Assessment and Gap Analysis for the Medscribe EMR, to ensure all regulatory FDA 21CFR, GXP, ICH and GAMP5 guidelines are met. Documentation of adverse event using MedWatch 3500a form- FDA Safety Information and Adverse Event Reporting Program. Maintain record integrity related to patient data and information in compliance with regulatory FDA, ICH and GXP Guidelines. Manage and troubleshoot problems related to documenting medical information in Amazing Charts – Electronic Medical Record software. Workflow integration between Amazing Charts – Electronic Medical Records (EMR), -Practice Management Software (PMS) and Electronic Document Management System (EDMS). Server and Software installation and management of database for the EMR, EDMS, PMS and CORI software.

Minimum Qualification Required:
Masters in Bio Technology, Bio Medical, Engineering, Pharmaceutical Sciences or Bachelors in Biotechnology, Bio Medical, Engineering, Pharmaceutical Sciences In Related Field With 5 Years Of Experience in the related field.

Email ID: hr@8kmiles.com