Job opening for Biotech Post Graruates

Ope j ings for Biotech Graduates. Salary starting from 10000/- in Research, QC, Production and Diagnostic Labs.
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Study of maillard reaction products in model aqueous and water/ethanol systems containing glucose and glycine, diglycine, and triglycine

Ji-Sang Kim, Young-Soon Lee

                                                                                     

Abstract

The reduction in pH was higher in aqueous solutions than in ethanolic solutions. Moreover, pH was lower in glycine compared to diglycine and triglycine in both aqueous and ethanolic solutions. Maillard reaction products (MRPs) derived from diglycine had a greater absorbance at 294 and 420 nm in ethanolic solution than an aqueous solution. The loss of glucose was higher in ethanolic MRPs solution than in aqueous solutions. The glycine oligomer content in ethanolic solutions remained much higher than that in aqueous solutions. Absorption in the ultraviolet (UV)-vis spectra was higher in MRPs derived from the ethanolic solution than in those derived from the aqueous solution. The molecular weights of MRPs derived from an ethanolic solution showed higher peak intensities than those derived from an aqueous solution, whereas the major peaks of the molecular weight in an ethanolic solution were slightly different from those in an aqueous solution.

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Keywords : lycine oligomer,Maillard reaction product,peptide chain length,ethanol.

Opening for Clinical Data Manager | Gurgaon

Organization Overview:

inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bioanalytical services, and strategic resourcing from a single clinical professional to an entire functional team.

Title:

Clinical Data Manager | Gurgaon

Position Overview:

Provides clinical data management support and advice.
Reports to Sr. Data Manager / Team Leader.
Works across international and functional boundaries as needed within a project team environment.
Works closely with Clinical, Medical, Statistics and Data Management team members.
 

Responsibilities:

Discrepancy/Query Management
Review Annotated CRF
Prepare, maintain and ensure the execution of Data Entry guidelines, Discrepancy/Edit Check documents, Quality Control Plans
Test and approve data entry screens
Test and approve discrepancy/edit checks
Track CRFs using electronic systems as required
Sign off on Database
Manage/Facilitate Final QC Activities
DB Lock/Unlock Activities
Creating the signature forms (Data Entry Receipt Log, Study Signature Log)
Maintaining Study Binder.
Communication with clinical sites to resolve outstanding data issues
Managing Study Timelines
Attend and participate in project team meetings
 

Requirements:

Bachelors degree in Life Sciences, Mathematics, Statistics, Computer Science or a Medical/Nursing qualification. 2-4 years of experience into Data Management activities (DE Screen Testing, Edit Check Creation and Testing, Query Management, Data Entry guidelines creation, DB Lock/Unlock) in the pharmaceutical industry or a clinical/health-related research organization. Understanding of clinical trial methodology and GCP. Experience and understanding of at least one clinical data management system (e.g. Clintrial, Oracle Clinical). Good verbal and written communication skills. Ability to work on multiple projects, plan, organize and prioritize activities. Knowledge of Framemaker, PL/SQL, Inform and/or EDC systems an additional plus.

City

Gurgaon

Country

India [IN]

Opening for Senior Clinical Research Associate

Organization Overview

inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bioanalytical services, and strategic resourcing.

Title

Senior Clinical Research Associate

Responsibilities

Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance
Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet-i3 SOPs and/or client guidelines
Recruit investigators
Negotiate study budgets with investigators
Obtain, review, and process regulatory and administrative documents from investigator sites
Review and develop protocols
Review and develop CRFs
Coordinate and present at Investigators’ Meetings
Participate in proposal meetings with potential clients
Prepare and review Serious Adverse Event (SAE) reports
Prepare project management reports for clients, project personnel, and PharmaNet-i3 management
Resolve issues, questions, and requests for additional study supplies
Review and approve monitoring trip reports
Review and verify completed CRFs
Review clinical data in-house
Resolve queries of CRF data with study site personnel
Review Tables and Listings generated from study data
Author Clinical Study Reports
Train and mentor CRAs on monitoring, internal procedures, and query resolution
When allocated by study management, submit essential/required documents to a central IRB or a country’s central Ethics Committee, and, if necessary based on local requirements, the Competent Authority.
 

Requirements

Bachelor’s Degree or nursing credential
over three and a half years experience in clinical research and direct monitoring experience required.
Fluent in English
Ability and willingness to travel 50% of the time
Excellent organizational skills
Ability to manage time and work independently
Excellent written and oral communication skills
 

City

Taipei

Country

Taiwan [TW]

Region

APAC

Opening for Technical Lead Clinical Data Management

Organization Overview:

inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bioanalytical services, and strategic resourcing.

Title:

Technical Lead Clinical Data Management

Responsibilities:

Provide clinical data management projects and oversight/advice to data management function in 50:50 ratios.
Verifies and approves time sheets of team members.
Distributes and assigns work to inVentiv Data Managers.
Update resource allocation sheet.
Assists with interviewing and training new hires as needed.
Conducts employee reviews for data management team as needed.
Attends and holds project team meetings as needed.
Attends GSK departmental meetings.
Works across international and functional boundaries as needed within a project team environment.
Works closely with Clinical, Medical, Statistics and Data Management team members.
Reviews timelines and ensure they are met.
Mentors, counsels, and recommends termination of subordinate employees as needed.
Works as Primary Data Manager (PDM) on individual projects.
 

Requirements:

Bachelors’ degree in Life Sciences, Mathematics, Statistics, Computer Science or a Medical/Nursing qualification.
Data management skills with 5 years clinical data management experience in the pharmaceutical industry or a clinical/health-related research organization.
Understanding of clinical trial methodology and GCP.
Experience and understanding of at least one clinical data management system (e.g. Clintrial, Oracle Clinical).
Good verbal and written communication skills.
Ability to work on multiple projects, plan, organize and prioritize activities.
Knowledge of Framemaker, Inform or any other EDC systems an additional plus.
 

City

Gurgaon

Country

India [IN]

Opening for Technical Lead SAS Programming

Organization Overview:

inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bioanalytical services, and strategic resourcing from a single clinical professional to an entire functional team.

Title:

Technical Lead SAS Programming

Position Overview

Provides SAS / Statistical programming support & advice.

Assists with interviewing and training new hires as needed.
Reports to Client’s Senior SAS Programmer / Team Leader.Distributes and assigns work to SAS Programming Team.
Works with departmental managers to develop plans and timelines.
Works across international and functional boundaries as needed within a project team environment.
Works closely with Statistics and Data Management team members.

Responsibilities:

Review protocols, CRFs, annotated CRFs, test databases and Statistical Analysis Plans.
Provide statistical programming support to team primarily using SAS software:
Develop, test and produce derived datasets, tables, listings and graphs for clinical study reports.
Validate derived datasets, tables, listings and graphs for clinical study reports.
Importing and exporting data files.
Extraction of data from database (e.g. Clintrial)
Assist with Quality Control Activities
Assist with development of departmental guidelines in line with the standardization of programs and systems for the generation of CSR components.
Reviews clinical study reports as needed.
Reviews timelines to ensure they are met.
Reviews training manuals and signs.
Attends departmental meetings.
Attends and holds project team meetings as needed.
Conducts employee reviews for SAS programming team as needed.
Mentors, counsels, and recommends termination of junior employees as needed.
Verifies and signs each individual team member’s attendance.
Works with management to approve vacation requests from team members.
Generate and maintain study documentation.
Attend and participate in project team meetings.

Requirements

Bachelors degree in Statistics, Computer Science, Mathematics or related discipline.
Good SAS programming skills with 3 years experience in the pharmaceutical industry or a clinical research organization. Skills should include Base SAS, SAS Macro and SAS ODS. Basic understanding of Software Development Lifecycle. Good verbal and written communication skills. Ability to work on multiple projects, plan, organize and prioritize activities.

City

Gurgaon

Country

India [IN]

Opening for Strategic Resourcing Quality Lead or Coordinator

Organization Overview:

inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bioanalytical services, and strategic resourcing.

Title:

Strategic Resourcing Quality Lead or Coordinator

Position Overview:

This role is involved in maintaining the QA compliance activities for FSP business.

Growth:

Will get exposed to QA activities in all BUs of FSP like data management, Clin Ops, SAS, Biostats etc
 

Responsibilities

Will be working in ICH and GCP environments
Should possess good communication skills
Involved in internal Audits
Potential candidate should have out of box thinking and wide perspective of company and role
Should be well versed with QA metrics
Should be GCP trained professional
Good to have global exposure

Requirements

For QA coordinator Candidates should have 2-3 years of experience in corporate QA preferably with FSP/ CRO experience and For QA lead candidate should have 5-6 years of experience in corporate QA.
Should have working experience in ICH and GCP environments
Should possess good communication skills
Preferred have prior Audit experience
Should be a good team player
Potential candidate should have out of box thinking and wide perspective of company and role 
Should be well versed with QA metrics
Should be GCP trained professional
Good have global exposure

City

Pune or Hyderabad

Country

India [IN]