Post : Consultant - Life Sciences - Regulatory Affairs
Job Description
• R&D, Regulatory Affairs, Medical Affairs, Pharmacovigilance, Market Access - Laboratory Information Management System (LIMS), Electronic Laboratory Notebook (ELN), Scientific Data Management System (SDMS), Collaborative drug discovery (CDD), Integrating data source management system, Clinical Trial Management System (CTMS), Regulatory Intelligence management systems (RIMS), Master Data Management (MDM), Document Management and submission management, Electronic Health Record, KOL mapping, publication planning,
• Horizontal consulting in life sciences: Program Management, Process Consulting, IT Strategy, Portfolio Rationalization, Customer Experience with respect to Regulatory Affairs value chain,What will you do?,At IC-LS, you will:,
• Be responsible for the delivery of business results to global pharmaceutical, medical devices and pharmaceutical distributors., ,
• Serve as a team member, track lead or engagement lead on business consulting engagements for clients.,
• Execute or lead consulting engagements in a global delivery model, working with consultants across regions.,
• Lead / contribute to sales pursuits, consulting offerings and internal initiatives.,
• Analyze problems, and structure complex business analyses. ,
• Perform Business Process Improvement using various business consulting tools and methodologies. ,
• Work with cross functional client teams to perform gap analysis and identify improvement options. ,
• Create detailed action plans that include organizational change management, resource planning, competitive strategies, and alliances to embark on a new strategic direction and to enable successful deployment of solutions. ,
• Lead client workshops to collaborate with client employees and educate them throughout the process.,
• Participate in a variety of Firm building events and the consultant referral program.,
• Build deep industry experience with thought leadershi
Job Description
• R&D, Regulatory Affairs, Medical Affairs, Pharmacovigilance, Market Access - Laboratory Information Management System (LIMS), Electronic Laboratory Notebook (ELN), Scientific Data Management System (SDMS), Collaborative drug discovery (CDD), Integrating data source management system, Clinical Trial Management System (CTMS), Regulatory Intelligence management systems (RIMS), Master Data Management (MDM), Document Management and submission management, Electronic Health Record, KOL mapping, publication planning,
• Horizontal consulting in life sciences: Program Management, Process Consulting, IT Strategy, Portfolio Rationalization, Customer Experience with respect to Regulatory Affairs value chain,What will you do?,At IC-LS, you will:,
• Be responsible for the delivery of business results to global pharmaceutical, medical devices and pharmaceutical distributors., ,
• Serve as a team member, track lead or engagement lead on business consulting engagements for clients.,
• Execute or lead consulting engagements in a global delivery model, working with consultants across regions.,
• Lead / contribute to sales pursuits, consulting offerings and internal initiatives.,
• Analyze problems, and structure complex business analyses. ,
• Perform Business Process Improvement using various business consulting tools and methodologies. ,
• Work with cross functional client teams to perform gap analysis and identify improvement options. ,
• Create detailed action plans that include organizational change management, resource planning, competitive strategies, and alliances to embark on a new strategic direction and to enable successful deployment of solutions. ,
• Lead client workshops to collaborate with client employees and educate them throughout the process.,
• Participate in a variety of Firm building events and the consultant referral program.,
• Build deep industry experience with thought leadershi
Candidate Profile
We are searching for success-oriented people who have a consulting mindset, strong analytical skills, a competitive drive, and an entrepreneurial spirit that will help propel the continued growth of the firm. We look for candidates that have prior relevant work experience, excel in ambiguous situations, and possess a passion for helping companies become more competitive. Business acumen combined with a comfort with technology is a must as well as strong verbal and written communication skills. Candidates must be able to quickly frame complex business problems and prioritize root causes with confidence, but not arrogance. We pride ourselves on hiring consultants that immediately fit into the fun yet professional atmosphere of Infosys. We value intellectual curiosity, initiative and entrepreneurial drive! Candidates must be open to domestic and international travel as per program requirements.
We are searching for success-oriented people who have a consulting mindset, strong analytical skills, a competitive drive, and an entrepreneurial spirit that will help propel the continued growth of the firm. We look for candidates that have prior relevant work experience, excel in ambiguous situations, and possess a passion for helping companies become more competitive. Business acumen combined with a comfort with technology is a must as well as strong verbal and written communication skills. Candidates must be able to quickly frame complex business problems and prioritize root causes with confidence, but not arrogance. We pride ourselves on hiring consultants that immediately fit into the fun yet professional atmosphere of Infosys. We value intellectual curiosity, initiative and entrepreneurial drive! Candidates must be open to domestic and international travel as per program requirements.
Additional Information
Qualification : B.Pharm, M.Pharm, M.Sc
Experience : 5+ years
Location : Hyderabad, Bangalore
Industry Type : Pharma
Functional Area : Life Sciences - Regulatory Affairs
End Date : 15th February, 2019
Qualification : B.Pharm, M.Pharm, M.Sc
Experience : 5+ years
Location : Hyderabad, Bangalore
Industry Type : Pharma
Functional Area : Life Sciences - Regulatory Affairs
End Date : 15th February, 2019
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