General Information

Organization: ePharmaSolutions LLC

Job Type: Full Time - Regular

Description and Requirements


The IT Project Manager at our Plymouth Meeting location will work closely with clients, and internal teams, to lead successful solution deployment lifecycle, from implementation through go-live, for major enterprise programs and provides support for WCG products.  When client projects involve two project management resources, their primary responsibility is to lead technology deployment through go-live.


To be considered for U.S.-based positions unless currently employed by WCG, where permitted by applicable law (including any applicable reasonable accommodation, medical or religious exemption), candidates must have received or be willing to receive the COVID-19 vaccine by start date.


·        Undertake strategy creation for contingency planning and risk mitigation

·        Responsible for running moderate to complex programs and projects

·        Defines requirements and plans the project life cycle deployment

·        Plans project life cycle deployment, based on effective information gathering from project team.

·        Responsible for planning and scheduling project goals, milestones and deliverable.

·        Help facilitate implementing business and system process best practices using the software as a service (SaaS) model for clients.

·        Manage relationship with business and executive stakeholders (internal and external).

·        Participate in strategic planning for new and existing products and services in support of overall corporate objectives.

·        Define and implement departmental process improvement plans to ensure competitive advantage and overall customer satisfaction.

·        Assist with responses to requests for proposal from prospective clients.

·        Support development of business analytics tools and measures.


·        Bachelor's degree, or equivalent, in computer sciences or a related field.


  • 5+ years relevant clinical trials/operations experience within a CRO or pharmaceutical research organization required; preferably in a project management related role
  • 2 years previous project management experience (preferred)

·        Working knowledge of Software Development Life Cycle (SDLC) and methodology

·        Working knowledge of GCP, ICH guidelines, and relevant FDA regulations

·        Working knowledge of clinical trial management process

·        Working knowledge of Clinical Trial Portals, their use and benefit

·        Experience with building and successfully managing client relationships