Job Description
Required Skills
Required Qualification
No of Positions Required : 4
Job Description
E-Merge tech is seeking .Net developer to assist in developing client projects
.Net Full Stack Developer with 2-4 years’ experience in ASP.Net, C#, MVC, Web API, Web Services, Linq, .Net Core, Micro Services, Angular JS, Java Script, jQuery, Multi-tier Architecture, Entity Framework, SQL, Design Patterns and Agile
Need to work collaboratively and independently together on projects to fulfill the requirements
Roles & Responsibilities
Skills
Required Qualification
Job Description
E-Merge tech is seeking highly Energetic, Dynamic and Research mindset analyst for Chemical Regulatory and Product compliance services.
Roles & Responsibilities
Skills
Required Qualification
Job Description
We have an opportunities for executives with at least 2 years’ experience in health economics or market access , within the pharmaceutical industry who are passionate about using their skills.
Roles & Responsibilities
Skills
Required Qualification
Salary
The primary role of the Associate is to support and provide Pharma Market research projects to give end-to-end insights (Disease landscape, forecast etc.) across given therapy area (Immunology, Oncology etc). The position reports to the client is based in Europe.
Roles & Responsibilities
E-Merge tech is seeking a Senior Data Curator to be a Lead on a project and provide solution for data curation.
Role involves reading scientific literatures, clinical trials, other related documents and curating or extracting information.
Roles & Responsibilities
To Extract Scientifically Important Information and Data from the Scientific Research Articles.
Required Qualification
Your role is to apply your skill & knowledge to fetch data from multiple online sources, standardize, cleanse and store it in DB
Need to understand the data sources on the web and to know exactly how, when, and which data to scrap, parse
Roles & Responsibilities
1 to 2 years experience in web crawling, BE/MCA or other degrees
Roles & Responsibilities
Regulatory Documents such as Clinical Study Reports (CSRs), Case Studies, Investigators Brochures (IBs) Protocol and other Regulatory medical writing, Data Science Analytics, Scientific and Research Writing, Blog Content Writing, Content Development.
Responsible for Authoring Clinical Evaluation Reports, Clinical Evaluation Plans, Post-Market Surveillance reports, and Periodic Safety Update Reports Literature Search, Screening, and Summarization of articles Perform data Fact check of the Documents authored Ensure Documents Comply with the Regulatory Requirements Participate, Project requirements Compliance to Quality, Confidentiality, and Security Adhere and follow Quality Systems, Processes and Policies Comply to Training and Specifications.
Required Qualification
Any Life science or Biomedical Graduate with 2 to 3 years of Experience.