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Subject Matter Expert Consultant 
(Job)

resume-library  |  United States  |  

Ref:
PARTNER-3XIV6I
Direct:
Employer:
Location:
United StatesUnited States (US)
Category:
Consulting/Consulting
Work Type:
Permanent
Work Time:
Full Time
Tags:
job,united-states,resume-library

Description 

Subject Matter Expert Consultant

 JOB DESCRIPTION



Summary/Objective :



We are seeking a motivated and experienced individual with a proven background in managing business consulting teams. They should possess analytic abilities, a robust and relevant background, strong presentation skills, relevant management experience and a team-oriented attitude.



As the Consultant, Consulting Services, you will have the responsibility to support business consulting projects, primarily in the Life Sciences Clinical domain. This role will support mapping current and future state business processes, gathering business requirements for systems such as electronic Trial Master File (eTMF), Clinical Trial Management Systems (CTMS), Risk-Based Quality Management (RBQM) and Study Start-up.



 



This role requires exceptional verbal and written communication skills and the candidate must have the ability to converse with people from all levels within an organization. We are looking for a creative and dedicated individual who will fit with our collaborative culture.



 



Principal Responsibilities :



To perform this job successfully, an individual must be willing and able to perform each essential responsibility satisfactorily.



Process analysis



Business/Functional Requirements analysis



Function point analysis to identify efficiency opportunities



Experienced with facilitation, and bring disparate views to a successful compromise in regards to desired capabilities and processes



Act as content Subject Matter Expert for business support of technology implementations



Support change management and communications activities



Foster a success-oriented, accountable environment within the company.



 Additional Skills



Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.



The candidate must be strong in communication, and must be able to prepare regular written and verbal presentations, technical documents, and reports.



The candidate must be able to work self-driven but must also work well in a team taking on different roles as needed (dependent on the project situation).



The candidate must be flexible and able to multitask; can work within an ambiguous, fast-moving environment, while also driving toward clarity and solutions; demonstrated resourcefulness in setting priorities and guiding investment in people and systems.



 Competencies



5+ years of minimum Clinical Operations and Clinical Development, and  information management consulting experience



Client engagement management and relationship building



A keen, flexible and aggressive intellect; superior conceptual thinking as well as analytical and problem solving skills



Experienced in validated systems implementations



Strong communication skills, both verbal and written, at all levels



Strong decision making, judgment and analytical skills



Demonstrated ability to effectively collaborate with cross-functional virtual teams



Experience working with applications for projects and Clinical activities (e.g. Veeva, , PhlexGlobal, IMPACT, Medidata, etc.)



Experience in the Regulatory Operations and/or Quality domains a plus, but not required



Certification on leading R&D technology platforms is a plus, but not required



Travel



Able to be present in the Danbury, CT office as required.



Able to travel to client sites across the US and potentially internationally when necessary.