Engagement Manager, Life Sciences Consulting

Tephra
Edison, NJ
Full-time
We are sorry. The job offer you are looking for is no longer available.

Description :

Experienced Consultant driving Advisory services Sales and Delivery, for Life Sciences companies. Provides specific domain expertise to guide clients in enterprise transformations, by defining a vision, and a roadmap for achieving the end state.Responsibilities :

  • Drives Advisory opportunity discovery and diagnostics. Helps shape an end state vision for clients’ businesses in one or more of : (i) Clinical, (ii) Regulatory (iii) Laboratory, (iv) Research areas
  • Guides clients in adoption of leading edge business processes and best practices; gets the best thinking from his / her staff and client team members, in their implementation
  • Confidently and effectively manages client stakeholders and Our Client resources to deliver results
  • Participates in supporting executive level client Steering Committee meetings; can manage conflict resolution among various stake holders / staff to successfully drive change management initiatives.
  • Where needed, in an owner or supporter role, drafts proposals, plans phased project execution, develops detailed project plans and manages program budgets and costs;

fosters shared accountability for results-based implementation plan

  • Facilitates the development of Life Sciences asset advancements by submissions to Our Client intellectual capital repository.
  • Mentors junior Associates and Analysts, as required, to ensure their rapid and successful professional developmentQualifications :
  • More than ten years of experience in the Life Sciences (LS) industry (incl. Pharma, Biotech, Medical Devices or Chemistry)
  • Strong experience in one or more of : (i) Clinical, (ii) Regulatory (iii) Laboratory, (iv) Research areas
  • For the domain area of expertise above, has a thorough understanding of Business Processes, KPIs, Challenges, and Industry Trends and Regulations
  • Nice to have : Experience in 2-3 additional LS specific domain areas from the following : SC / Manufacturing, R&D, Clinical Supplies, Validation, ERP, LIMS, Program / Project Management, IoT, Digital Experience, IT architecture
  • Has experience with IT enablement and business transformations, and a holistic knowledge of Business and IT Landscape for the domain area of experience above.
  • Has familiarity with conducting Business Process Reviews, Business Process Improvements, IT Landscape Assessment, IT simplification, driving the adoption of new technology
  • More than five years of experience in business development, client relationship management and program / project management
  • Familiar with usual office software plus selected or dedicated (as per focus area above) relevant domain specific packages
  • Strong team building skills, strategy and operations thinking, solution & result orientation, intercultural competence
  • Direct working experience in the LS related industry for minimum 4 years or PhD / Domain specific engineering degree with practical experience.
  • Excellent verbal and written communication skills
  • Excellent presentation skills development and delivery
  • Good public speaking / publishing record
  • 2 days ago
Related jobs
Promoted
Maritz Research Inc
Plainsboro Township, New Jersey

The Medical Meeting Manager works effectively with internal Colleagues/Brand Management /Trial Managers/International Trial Managers/International Colleagues as required for advisory boards, clinical investigator meetings and events, speaker bureau training meetings, meetings in conjunction with con...

Promoted
Randstad Life Sciences US
Bridgewater, New Jersey

We are seeking Director of Project Management whom will provide Project Management to the current portfolio of projects, and work with contract manufacturers both in the US and abroad.Experience with Generics or CMO/CDMO is highly preferred.This is a very hands-on role in a small department with a t...

Promoted
IPS-Integrated Project Services, LLC
Franklin Township, New Jersey

Its newest acquisition, Linesight, specializes in cost, schedule, risk, program, and project management services in various market sectors, including data centers, life sciences, and high-tech industries. May work with the Senior Project Managers or Directors on a larger project. Through operational...

Katalyst HealthCares & Life Sciences
South Plainfield, New Jersey

Serve as the CMC Product Lead for assigned products and be accountable for the delivery of all regulatory milestones for assigned products through the product lifecycle as needed for product in-license/due diligence review, product divestment and product withdrawal. Manage execution / authoring of C...

GForce Life Sciences
New Jersey, US

Our mid-sized, growing pharmaceutical client is seeking a seasoned project/program management professional who can manage delivery of the Connected Health portfolio of projects for the organization.Ensure everything runs smoothly, i.General Duties / Expectations of Role:.Formulate, organize, and mon...

Katalyst HealthCares & Life Sciences
South Plainfield, New Jersey

Manager of Regulatory Compliance will support the Sr. Manage GRS training curricula and LMS training metrics in collaboration with GRS line managers. ...

Katalyst HealthCares & Life Sciences
Princeton, New Jersey

Lead the creation of the Data Review and Cleaning Plan and development of the data cleaning strategy.Provide oversight of the data validation plan and provide DM insight to maximize the data validation strategy.Review CRFs to ensure alignment with protocol; lead and perform sponsor acceptance testin...

Katalyst HealthCares & Life Sciences
South Plainfield, New Jersey

Under limited supervision, works collaboratively with vendor Project Managers and Clinical Data Managers to assure that Data Management functions are performed in compliance with regulations and according to study protocol and Study Data Management Manual (DMM). Manages coordination of CRO data mana...

Katalyst HealthCares & Life Sciences
South Plainfield, New Jersey

Essential Duties and Responsibilities:.Provide guidance to the Transparency team on overall Clinical Trial processes and conduct.Perform required clinical trial registration and/or results disclosure activities as necessary.Assess the overall process between the Clinical Management team and the CTT&...

Katalyst HealthCares & Life Sciences
Woodbridge Township, New Jersey

Serve as lead CDM on assigned clinical trials by attending internal and external clinical trial project team meetings.Responsible for the study-specific data management tasks from protocol review to database lock to ensure data are collected , reviewed, and delivered with high quality, on-time, and ...