Pharmacovigilance Reviewer
Position Pharmacovigilance Reviewer Reporting to Team Leader or Manager Qualifications / Work Experience Formal Education
• Graduate, preferably in science
• Bachelor’s degree / Masters in Life sciences
• MBBS/BHMS/ BAMS/ BDS/ Paramedical degrees
• B. Pharm/ M. Pharm
• Bachelors / Masters in Clinical research
• University degree in pharmaceutical sciences or other relevant
medical or scientific disciplines preferred
Certifications
• Certifications / Diploma in IT &/ CDM
Work Experience
• Previous Pharmacovigilance / ICSR processing experience
Candidate having equivalent qualifications, training & experience may be considered.
Essential Competencies (Knowledge, Skills and Attributes) Expected Competency Domain
• Good technical knowledge of medical terminology
• Compliant with GCP/GCDMP
• Computer and Internet skills and experience (familiarity and comfort with MS Office products)
• Oral and written English communication skills
• Self-motivated and enthusiastic
Accountability Domain
• Understand and comply with Standard Operating Procedures
• Anticipate problems, issues, and proactively work to minimize the impact
• Maintenance of strict confidentiality in all CAC-India projects
• Responsible for Data Quality
• Accountable for customer satisfaction of all CAC-India stakeholders
• Build constructive and effective relationships with study team, departmental associates and others (both inside and outside the company).
Key Responsibilities: Safety Data Processing
• Review and Assess all source documents and compile data in an adverse event report mentioned in the ICSR
• Oversees and performs and ensures case receipt and triage activities are completed for Individual Case Safety Reports (ICSRs) from all sources and ensure this is performed in a timely manner Data enter report into the client safety database
• Concentrate on quality of work to get error free data
• Code averse events in the client safety database
• Responsible for and ensures the reconciliation of the safety database with ICSR source files
• Release reports to client through client safety database
• May be asked to perform ICSR case processing activities as a backup for safety information cases (including initial data entry of safety information, initial determination of seriousness, expectedness, listedness, and Reportability.)
• Effective communication with study teams and departmental associates
• Check labelling and correct the information
• Submit the report as per the timelines
• Participates in or assists in leading special projects and process development or improvement activities
• Provide support for business owner of global safety database and related systems (i.e. testing and validation, identification of database enhancements, change control activities.)
Additional Information Industry type
• Pharma/ Biotech/ Clinical research
Functional Area
• Life scienceLocation Mumbai Working Hours As per company policy or depending on Project requirement Travel Not Required Job Code R145 E-mail This email address is being protected from spambots. You need JavaScript enabled to view it. Sub Line REQ 2019 Q4 R145 Ref: (usindia)
Clinical Data – Team Manager
Position Clinical Data – Team Manager Reporting to General Manager Qualifications / Work Experience Formal Education
• Graduate, preferably in science
• Bachelor’s degree / Masters in Life sciences,
• MBBS/BHMS/ BAMS/ BDS/ Paramedical degrees,
• B. Pharm/ M. Pharm
• Bachelors / Masters in Clinical research
Certifications
• Certifications / Diploma in IT &/ CDM
Work Experience
• Previous experience as a Biometrician/ Senior Biometrician 3 – 4 years.
Candidate having equivalent qualifications, training & experience may be considered.
Essential Competencies (Knowledge, Skills and Attributes) Expected Competency Domain
• Good technical knowledge of medical terminology.
• Compliant with GCP/GCDMP.
• Computer and Internet skills and experience (familiarity and comfort with MS Office products).
• Understanding database/programming concepts.
• Able to use SQL and other programming/query languages.
• Oral and written English communication skills.
• Self-motivated and enthusiastic.
• Ability to develop and deliver presentations.
• Knowledge of clinical trial principles, methodology and procedures.
• Knowledge of all federal, state regulations and guidelines pertaining to the conduct of clinical trials on human subjects.
• Knowledge of current and developing trend and standards in clinical trials monitoring.
• Ability to independently develop novel concepts and techniques in Data management techniques.
• Ability to establish and maintain effective working relationships with co-workers, managers and clients.
• Experience in effectively managing multiple tasks simultaneously.
• Effective problem solving skills is a position requirement.
Accountability Domain
• Good technical knowledge of the process of CDMS (e.g. Clintrial, Oracle Clinical).
• Understand and comply with Standard Operating Procedures.
• Anticipate problems, issues, and proactively work to minimize the impact.
• Maintenance of strict confidentiality in all CAC-India projects.
• Is accountable for achieving deliverables for a project meeting timelines & quality standards required.
• Ensures high performance and efficiency of the team through ongoing mentoring of DM team.
Key Responsibilities: Clinical Data Processing
• Provide study status reports to head of the department.
• Maintain current knowledge of company standard operating procedure (SOP) and participate in development and review of all SOPs.
• Perform all duties and responsibilities in accordance with GCP guidelines, regulations, statutes and SOPs.
• Establish appropriate Data Management tools and processes for the study team.
• Work collaboratively with other functional groups (Clinical Operations, pharmacovigilance, quality assurance, biostatistics) in the organizations within the trials.
• Provide ongoing training and support to the Data Management team through establishment of study tools and training materials, frequent team meetings, and regular communication.
• Identify quality issues during the study through regular review of the Data Management team communications & institute appropriate corrective action plans.
• Communicate and establish a customer service relationship with the clinical client representative as appropriate.
• Define resource requirements and work with supervisor to prioritize resource assignments across projects.
• Provides review and guidance for production of Data Management documentation or deliverables that are produced by the Data Management Function.
• Provides technical advice and solutions with internal and external customers to solve problems and improve efficiency.
• The position is required to participate in the implementation of new processes and technology.
• Ensures that staff is trained and compliant with current operating procedures and work instructions and project scope of work.
• Identification of professional development/training needs of staff are required to be addressed by the Manager.
• Mentoring staff members to develop Data Management process and system expertise is a requirement of the position.
• Primary customer interactions at project level with a focus on specific Data Management Function with established customers provide operational input into proposals and scope of work is a position expectation.
• May participate in customer meetings and lead discussions of project requirements and strategic planning.
• Understand scope of work, budget, and scope assumptions.
• Identify out of scope work and contribute to estimating costs of this work.
• Ensuring project milestones pertaining to Data Management Function are met according to agree upon timelines with high quality is a position expectation.
• May spend significant time performing work tasks associated with Data Management Function, typically in a lead role.
• Manage delivery of projects through full data management study life-cycle (with minimal guidance).
• With guidance from Manager, manage project timelines and quality; determine resource needs; identify out-of scope work.
• Perform database designer activities for technologies not requiring extensive programming.
• Perform comprehensive quality control procedures.
• Assist in developing and implementing new technology.
• Meet objectives as assigned.
Additional Information Industry type
• Pharma/ Biotech/ Clinical research
Functional Area
• Life science
Experience
• 6 to 8 years of ExperienceLocation Mumbai Working Hours As per company policy or depending on Project requirement Travel Not Required Job Code R144 E-mail This email address is being protected from spambots. You need JavaScript enabled to view it. Sub Line REQ 2019 Q4 R144 Ref: (usindia)
Pharmacovigilance Coordinator
Position Pharmacovigilance Coordinator Reporting to Team Leader or Manager Qualifications / Work Experience Formal Education
• Graduate, preferably in science
• Bachelor’s degree / Masters in Life sciences
• MBBS/BHMS/ BAMS/ BDS/ Paramedical degrees
• B. Pharm/ M. Pharm
• Bachelors / Masters in Clinical research
• University degree in pharmaceutical sciences or other relevant medical or scientific disciplines preferred
Certifications
• Certifications / Diploma in IT &/ CDM
Work Experience
• Previous Data Entry experience preferred
Candidate having equivalent qualifications, training & experience may be considered.
Essential Competencies (Knowledge, Skills and Attributes) Expected Competency Domain
• Good technical knowledge of medical terminology.
• Compliant with GCP/GCDMP.
• Computer and Internet skills and experience (familiarity and comfort with MS Office products).
• Oral and written English communication skills
• Self-motivated and enthusiastic.
Accountability Domain
• Understand and comply with Standard Operating Procedures.
• Anticipate problems, issues, and proactively work to minimize the impact.
• Maintenance of strict confidentiality in all CAC-India projects.
• Responsible for Data Quality.
• Accountable for customer satisfaction of all CAC-India stakeholders.
• Build constructive and effective relationships with study team, departmental associates and others (both inside and outside the company).
Key Responsibilities: Safety Data Processing
• Review and Assess all source documents and compile data in an adverse event report
• Ensure the completeness of the documents, clinical safety data during data entry and tracking and interact with seniors on timely basis for further clarification if there are any discrepancies.
• Oversees and performs and ensures case receipt and triage activities are completed for Individual Case Safety Reports (ICSRs) from all sources and ensure this is performed in a timely manner Data enter report into the client safety database
• Interact with seniors for additional responsibilities other than Study Documents Tracking and Data Entry.
• Concentrate on quality of work to get error free data.
• Responsible for and ensures the reconciliation of the safety database with ICSR source files.
• Release reports to client through client safety database.
• May be asked to perform ICSR case processing activities as a backup for safety information cases (including initial data entry of safety information, initial determination of seriousness, expectedness, listedness, and Reportability.)
• Perform other related duties as required.
• Effective communication with study teams and departmental associates.
Additional Information Industry type
• Pharma/ Biotech/ Clinical research
Functional Area
• Life science
Experience
• Fresher or up to 1/1.5 years of ExperienceLocation Mumbai Working Hours As per company policy or depending on Project requirement Travel Not Required Job Code R143 E-mail This email address is being protected from spambots. You need JavaScript enabled to view it. Sub Line REQ 2019 Q4 R143 Ref: (usindia)
Clinical Data Reviewer / Validator
Position Clinical Data Reviewer / Validator Reporting to Team Leader or Manager Qualifications / Work Experience Formal Education
• Graduate, preferably in science
• Bachelor’s degree / Masters in Life sciences,
• MBBS/BHMS/ BAMS/ BDS/ Paramedical degrees,
• B. Pharm/ M. Pharm
• Bachelors / Masters in Clinical research
Certifications
• Certifications / Diploma in IT &/ CDM
Work Experience
• Previous experience as a Biometrician/ Senior Biometrician 3 – 4 years.
Candidate having equivalent qualifications, training & experience may be considered.
Essential Competencies (Knowledge, Skills and Attributes) Expected Competency Domain
• Good technical knowledge of medical terminology.
• Compliant with GCP/GCDMP. • Computer and Internet skills and experience (familiarity and comfort with MS Office products). • Understanding database/programming concepts.
• Able to use SQL and other programming/query languages.
• Oral and written English communication skills
• Self-motivated and enthusiastic.
Accountability Domain
• Good technical knowledge of the process of CDMS (e.g. Clintrial, Oracle Clinical).
• Understand and comply with Standard Operating Procedures.
• Anticipate problems, issues, and proactively work to minimize the impact.
• Maintenance of strict confidentiality in all CAC-India projects.
• Responsible for Data Quality.
• Accountable for customer satisfaction of all CAC-India stakeholders.
• Build constructive and effective relationships with study team, departmental associates and others (both inside and outside the company).
Key Responsibilities: Clinical Data Processing
• Verify data in the clinical database using CRFs and DCFs.
• Receive feedback from HOD, learn from errors and apply corrections.
• Ensure the completeness and validity of the clinical trial data that has gone through data entry.
• Respond and complete data queries and clarifications identified by the system or through manual checks as identified in the data validation guidelines.
• Propose data clarification forms to clinical trial sites for mentor review.
• Guide new candidate to carry out data entry and validation.
• Interact with the clients regarding data quality issues.
• Participate in the development of project related documents (e.g. Data Entry guidelines, Data validation guidelines etc.)
• Maintain appropriate validation documentation.
• Investigate and troubleshoot problems and determine solutions.
• Perform other related duties as required.
• Effective communication with study teams and departmental associates.
Additional Information Industry type
• Pharma/ Biotech/ Clinical research
Functional Area
• Life science
Experience
• Up to 2 - 4 years of ExperienceLocation Mumbai Working Hours As per company policy or depending on Project requirement Travel Not Required Job Code R141 E-mail This email address is being protected from spambots. You need JavaScript enabled to view it. Sub Line REQ 2019 Q4 R141 Ref: (usindia)
Clinical Data Coordinator
Position Clinical Data Coordinator Reporting to Team Leader or Manager Qualifications / Work Experience Formal Education
• Graduate, preferably in science
• Bachelor’s degree / Masters in Life sciences
• MBBS/BHMS/ BAMS/ BDS/ Paramedical degrees
• B. Pharm/ M. Pharm
• Bachelors / Masters in Clinical research
Certifications
• Certifications / Diploma in IT &/ CDM
Work Experience
• Previous Data Entry experience preferred.
Candidate having equivalent qualifications, training & experience may be considered.
Essential Competencies (Knowledge, Skills and Attributes) Expected Competency Domain
• Good technical knowledge of medical terminology.
• Compliant with GCP/GCDMP.
• Computer and Internet skills and experience (familiarity and comfort with MS Office products).
• Oral and written English communication skills
• Self-motivated and enthusiastic.
Accountability Domain
• Good technical knowledge of the process of CDMS (e.g. Clintrial, Oracle Clinical).
• Understand and comply with Standard Operating Procedures.
• Anticipate problems, issues, and proactively work to minimize the impact.
• Maintenance of strict confidentiality in all CAC-India projects.
• Responsible for Data Quality.
• Accountable for customer satisfaction of all CAC-India stakeholders.
• Build constructive and effective relationships with study team, departmental associates and others (both inside and outside the company).
Key Responsibilities: Clinical Data Processing
• Verify data in the clinical database using CRFs and DCFs.
• Ensure the completeness of the documents, clinical trial data during data entry and tracking and interact with seniors on timely basis for further clarification if there are any discrepancies.
• Interact with seniors for additional responsibilities other than Study Documents Tracking and Data Entry.
• Concentrate on quality of work to get error free data.
• Participate in the development of project related documents (e.g. Data Entry guidelines, Data validation guidelines etc.)
• Perform other related duties as required.
• Effective communication with study teams and departmental associates.
Additional Information Industry type
• Pharma/ Biotech/ Clinical research
Functional Area
• Life science
Experience
• Fresher or up to 1/1.5 years of ExperienceLocation Mumbai Working Hours As per company policy or depending on Project requirement Travel Not Required Job Code R140 E-mail This email address is being protected from spambots. You need JavaScript enabled to view it. Sub Line REQ 2019 Q4 R140 Ref: (usindia)
Java Senior Programmer (3+ yrs )
Position Java Senior Programmer Skills Technical Knowledge of Core Java, Advanced Java, JSP/Servlet, Strut 1 Framework, Hibernate Framework
Preferred additional Skill: Knowledge of Struts 2, Spring Framework, Java Swings, Java Networking
Japanese - DesiredJob Description Will be leading a team technically. Involves in technical training of the team. Should be able to understand Detail design and able to create Detail design documents. Experience 3 yrs (Out of at least 2 years Java) Education BE/B.Tech/MCA Location Ahmedabad and Indore Job Code R107 E-mail 
Sub Line REQ 2014 Q4 R107 Ref: (usindia)
Dot Net Senior Programmer(3+ yrs)
Position Senior Programmer/ TL (Dot Net) Skills Technical Knows following computer languages proficiently VB, ASP, Dotnet. Database like Oracle, MS SQL Server, Sybase, Mysql
Japanese - DesiredJob Description Will be leading a team technically. Involves in technical training of the team. Should be able to understand Detail design and able to create Detail design documents. Experience 3 yrs (Out of at least 2 years Dot Net) Education BE/B.Tech/MCA Location Ahmedabad,Indore Job Code R108 E-mail Sub Line REQ 2014 Q2 R108 Ref: (usindia)
Application development(Project Leader / System Engineer, 5+ years)
Position Project Leader / System Engineer Skills Requirement gathering and specification writing,
Good communication, Programming, Testing, Web development knowledge
Languages: Java
DB: SQL, OracleJob Description Functional Role - Requirement gathering and specification writing,
Good communication, Programming, Testing, Web development knowledge
Japanese skills JLPT N2 or above Experience 5+ years Education Graduate Location Tokyo and nearby Work Period 2013/2 to long term Job Code RJ01 E-mail 
Sub Line REQ 2012 Q4 RJ01 Ref: (usindia)
Application development(Java Programmer 3+ years)
Position Programmer Skills Good communication, Programming, Testing, Web development knowledge
Languages: Java
DB: SQL, OracleJob Description Good communication, Programming, Testing , Web development knowledge Japanese skills JLPT N3 or above Experience 3+ years Education Graduate Location Tokyo and nearby Work Period 2013/2 to long term Job Code RJ02 E-mail Sub Line REQ 2012 Q4 RJ02 Ref: (usindia)
Web application development(Programmer 3+ years)
Position Programmer Skills Android Java development JLPT Level 3 + Job Description Good communication, Programming, Testing , Web development knowledge Experience 3+ years Education Graduate Location Tokyo and nearby
Job CodeRJ02 E-mail Sub Line REQ 2011 Q3 RJ02 Ref: (usindia)
Web application development(Project Leader / System Engineer, 5+ years )
Position Project Leader / System Engineer Skills Android Java development JLPT Level 2 or above Job Description Functional Role - Requirement gathering and specification writing, Good communication, Programming, Testing, Web development knowledge Experience 5+ years Education Graduate Location Tokyo and nearby
Job CodeRJ01 E-mail Sub Line REQ 2011 Q3 RJ01 Ref: (usindia)
Application development(VB.Net, C#.Net, 3+ years)
Position Programmer Skills Good communication, Programming, Testing, Web development knowledge
Languages: VB.Net, C#.NetJob Description Functional Role - Requirement gathering and specification writing,
Good communication, Programming, Testing, Web development knowledge
Japanese skills JLPT N3 or above Experience 3+ years Education Graduate Location Tokyo and nearby Work Period 2013/2 to long term Job Code RJ03 E-mail Sub Line REQ 2012 Q4 RJ03 Ref: (usindia)
Application development (C, C++, 3+ years)
Position Programmer Skills C, C++, VC JLPT Level 3 + Job Description Good communication, Programming, Testing , Web development knowledge Experience 3+ years Education Graduate Location Tokyo and nearby Job Code RJ03 E-mail Sub Line REQ 2011 Q3 RJ03 Ref: (usindia)
Application development (Ruby on Rails, 2+ years)
Position Programmer Skills Ruby on Rails JLPT Level 3 + Job Description Good communication, Programming, Testing , Web development knowledge Experience 2+ years Education Graduate Location Tokyo and nearby Job Code RJ04 E-mail Sub Line REQ 2011 Q3 RJ04 Ref: (usindia)
Dot Net Analyst Programmer(5+ yrs)
Position Dot Net Analyst Programmer Skills Technical - Knows following computer languages proficiently:
VB, ASP, Dotnet. Database like Oracle, MS SQL Server,
Sybase, Mysql, other Project planning tools
like MS project. Able to do scheduling
Japanese - Level 3(N4) is desirableJob Description Functional Role - Project Leader
1. To manage the project team and lead the implementation of projects, through effective inter-departmental co-ordination,continuous monitoring and improvements.
2. Ensuring of standard routines are followed, offering preventive and post incidence support.
3. Manage routine functions like estimation, scheduling, resource allocation/de-allocation, etc
4. Receive, process, and ensure confidentiality of sensitive information and materials
5. Maintain access rights for Project VSS.
6. Define, analyse, approve/re-approve, release and distribute documents related to project ,to improvise current policies & facilities provided to team members.
7. To co-ordination with client or onsite SE, internal groups for the project.
8. To identify and request for human resource requirements
9. Strategically plan, manage, monitor project and the teams within the project for timely, effective and quality oriented results.
10. To ensure all project deliveries to the customers/ Onsite SE are done in timely manner.Experience 5+ yrs Education B.E. / MCA / B.Sc./Diploma or Equivalent Location Mumbai Job Code R88 E-mail Sub Line REQ 2010 Q1 R88 Ref: (usindia)
Dot Net System Analyst(8+ yrs)
Position Dot Net System Analyst Skills
Technical - Knows following computer languages proficiently:
VB, ASP, Dotnet. Database like Oracle, MS SQL Server, Sybase, Mysql,
other Project planning tools like MS project.
Able to do scheduling. Japanese - Level 3(N4) is desirableJob Description Job Description Functional Role - Project Leader
1. To manage the project team and lead the implementation of projects, through effective inter-departmental co-ordination,continuous monitoring and improvements.
2. Ensuring of standard routines are followed, offering preventive and post incidence support.
3. Manage routine functions like estimation, scheduling, resource allocation/de-allocation, etc
4. Receive, process, and ensure confidentiality of sensitive information and materials
5. Maintain access rights for Project VSS.
6. Define, analyse, approve/re-approve, release and distribute documents related to project ,to improvise current policies & facilities provided to team members.
7. To co-ordination with client or onsite SE, internal groups for the project.
8. To identify and request for human resource requirements
9. Strategically plan, manage, monitor project and the teams within the project for timely, effective and quality oriented results.
10. To ensure all project deliveries to the customers/ Onsite SE are done in timely manner.Experience 8+ yrs Education B.E. / MCA / B.Sc./Diploma or Equivalent Location Mumbai Job Code R89 E-mail Sub Line REQ 2010 Q1 R89 Ref: (usindia)
Java Analyst Programmer(5+ yrs )
Position Java Analyst Programmer Skills
Technical - Knows following computer languages proficiently:
Java, JSP. Database like Oracle, MS SQL Server, Sybase, Mysql,
other Project planning tools like MS project.
Able to do scheduling Japanese - Level 3(N4) is desirableJob Description Functional Role - Project Leader
1. To manage the project team and lead the implementation of projects, through effective inter-departmental co-ordination,continuous monitoring and improvements.
2. Ensuring of standard routines are followed, offering preventive and post incidence support.
3. Manage routine functions like estimation, scheduling, resource allocation/de-allocation, etc
4. Receive, process, and ensure confidentiality of sensitive information and materials
5. Maintain access rights for Project VSS.
6. Define, analyse, approve/re-approve, release and distribute documents related to project ,to improvise current policies & facilities provided to team members.
7. To co-ordination with client or onsite SE, internal groups for the project.
8. To identify and request for human resource requirements
9. Strategically plan, manage, monitor project and the teams within the project for timely, effective and quality oriented results.
10. To ensure all project deliveries to the customers/ Onsite SE are done in timely manner.Experience 5+ yrs Education B.E. / MCA / B.Sc./Diploma or Equivalent Location Mumbai Job Code R93 E-mail Sub Line REQ 2010 Q1 R93 Ref: (usindia)
Java System Analyst Programmer(8+ yrs )
Position Java System Analyst Programmer Skills Technical - Knows following computer languages proficiently:
Java, JSP. Database like Oracle, MS SQL Server, Sybase, Mysql,
other Project planning tools like MS project. Able to do scheduling Japanese - Level 3(N4) is desirableJob Description Functional Role - Project Manager
1. To manage the teams and lead the implementation of group activities,through effective interdepartmental co-ordination, continuous monitoring and improvements.
2. Ensuring of standard routines are followed, offering preventive and post incidence support.
3. Manage routine functions like estimation, scheduling, resource allocation/de-allocation, etc
4. Receive, process, and ensure confidentiality of sensitive information and materials
5. Maintain access rights for Project VSS.
6. Define, analyse, approve/re-approve, release and distribute documents related to projects to improvise current policies & facilities provided to team members.
7. To co-ordination with client or onsite SE, internal groups for the projects.
8. To identify and request for human resource requirements
9. Strategically plan, manage, monitor projects and the teams of the projects for timely, effective and quality oriented results
10. Analyse customer requirements and providing Technical solution to the development teams.Experience 8+ yrs Education B.E. / MCA / B.Sc./Diploma or Equivalent Location Mumbai Job Code R94 E-mail Sub Line REQ 2010 Q1 R94 Ref: (usindia)
Programmer for iPhone/iPad/Andriod(3+ yrs )
Position Programmer for iPhone/iPad/Andriod Skills Technical - Knows following computer languages proficiently:
Objective C ,C,C++/Java, other Project planning tools
like MS project. Able to do scheduling.Job Description Functional Role - Team Member
1. Strategically plan, manage, monitor project requirements
and give timely, efficient, robust and maintainable
quality-oriented results in deliveries and implementation.
2. Ensuring of standard routines are followed, offering
preventive and post incidence support.
3. Manage routine functions like reviews, trainings,
status reporting, etc and its activity logs.
4. Receive, process, and ensure confidentiality of sensitive
information and materials.
5. Assist in maintaining access rights, documents, activity logs
of Project VSS.
6. Analyse documents released related to project .
7. To co-ordination with internal groups for the project.
8. Assist in code reviews, analysis of design changes and
impacts, during delivery and implementation.Total Experience 3+ yrs Experience 0.5+yrs Relevant to Technology Education B.E. / MCA / B.Sc./Diploma or Equivalent Location Mumbai Job Code R95 E-mail Sub Line REQ 2010 Q1 R95 Ref: (usindia)
