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AVP Role-Service Delivery Clinical Data Management

13.00 to 20.00 Years   Bangalore   18 Dec, 2020
Placewell Consultants
Job LocationBangalore
EducationNot Mentioned
SalaryNot Disclosed
IndustryIT - Software
Functional AreaGeneral / Other Software,Sales / BD
EmploymentTypeFull-time

Job Description

Job Description Life Sciences (LS) R&D Operations SERVICE DELIVERY LEAD (SDL) ROLEDo you have a passion to re-imagine Future of LS R&D, design Best in class LS Processes and shape large scale Digital LS transformations Accenture is the Industry leader in Life Sciences BPS serving to Fortune 500 clients across US, Europe, LATAM and APAC from our 13 Global Delivery centers. Our demand is rapidly increasing and therefore, we are looking to strengthen our team of LS deep domain experts with hands on experience of shaping large scale deals, driving digital LS R&D transformation for Fortune 500 clients. Apply for the new now!Are you the trusted advisor to the Senior LS R&D leadership and leader we are looking for

  • You must be a Clinical Domain expert
  • You must have hands on experience and have managed large scale End to End LS service delivery for global Clients
  • You must be well versed with Industry Digital LS technologies & leading tools, automation, AI and Analytics plus already have a proven track record of implementing Digital LS solutions.
  • You must have strong delivery and business excellence orientation in LS
  • You excel in developing strong client relationships, drive client dialogue both at function leadership and at CXO level, and in shaping and delivering value-led LS projects.
  • You are a solid team player who thrives when working in a fast-paced, high energy and project-oriented environment and accustomed to driving outcomes in matrixed organization structures.
  • You have excellent leadership and communication skills with extensive experience in managing a high-performance team and delivering large scale transformation projects.
  • You are an action and results-oriented, self-driven person with a high energy level, analytical and structured, quality focused and adaptable.
  • You are flexible and capable of some travel.
  • You can do process diagnostics, blueprinting and are savvy with power-point and Excel.
Required Educational Background:
  • Bachelor s degree preferred in one or more of the following disciplines or related fields: Life Sciences and Allied Healthcare professionals.
    • Required Software Tool Competencies: Basic office tools (e.g. MS Suite); CDMS (e.g. Medidata Rave, Oracle Clinical, INFORM etc.); J-Review; SAS programming will be a plus.Required Experience & Competencies:
  • 12+ years of extensive experience as a Delivery Manager or equivalent in the pharmaceutical industry
  • Experience negotiating with and influencing others to meet challenging goals. Must be self-motivated, with the ability to follow through on assignments without direct supervision, very attentive to detail, capable at multitasking across projects and able to effectively contribute in a team environment.
  • Experience working with vendors who supply clinical data in electronic format.
  • Strong analytical skills to facilitate detecting and resolving data problems encountered in clinical research studies
  • Previous experience using project management techniques including prioritization methods and the ability to work on different projects simultaneously.
  • Previous experience working in a team environment within a matrix organization.
  • In depth knowledge of clinical research including Investigator site issues, important milestones and strategies to ensure timelines are met.
  • Experience in effective implementation of data review/management plans/documents and document preparation.
  • Experience in all aspects of data management from CRF design to database lock within expectations set by management.
  • Knowledge of data review processes and Database Management Systems including eDC systems.
  • Knowledge of ICH-GCP guidelines regulatory guidelines/regulations.
  • Solid understanding of regulations, GCPs, 21CFR Part 11 and data privacy as they apply to data handling and the use of computer systems in clinical research.
  • Advanced Knowledge of general clinical research including Investigator site processes.
  • Advanced Knowledge of the pharmaceutical industry including the clinical and regulatory components.
  • Advanced Knowledge of project planning and management methods.
    • ,

    Keyskills :
    project planningat multitaskingdata managementcrf designclinical researchhigh energy levelfortune 500oracle clinicalservice deliverydata privacystrong analytical skillslife sciencesmedidata ravelarge scale transformationglobal deliverysas p

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