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Title : MKG- Project Specialist - Scientific III -246
State : Pennsylvania   Date : Feb 26, 2021
Experience Level :  
Position Type : Project Specialist - Scientific III      
Description
This position is for a leading pharmaceutical company. Below are the details of the engagement. If you are available and interested please send me your updated word resume & your expected hourly rate on W2 ASAP.
Looking forward to hearing from you soon.

Work Location: North Wales, PA

Job Title: Project Specialist - Scientific III

Duration: 23+ months (extendable) contract on W2


Responsibilities:

Under general supervision of the Sr. Specialist or Associate Director within Study Management - Strategy & Operations at the Center for Observational and Real-World Evidence (CORE), the study manager provides support to a number of Scientific CORE Lead Scientists across multiple Therapeutic Areas and divisions. Support includes operational tasks associated with the execution of observational research studies conducted within CORE, part of the Client. The study manager may participate in ad-hoc requests (e.g. data analytics and visualization, quality control measures, and other business-related tasks) as needed.

Key Functions:
  • Coordinate compliance and operational tasks in support of non-interventional research activities.  Main responsibilities include:
  • Managing compliance activities related to publication development and archival of all required documentation in internal repository (e.g. Datavision)
  • Coordinating contracting and budget management activities related to confidentiality and consultant agreements
  • Assisting with the development and planning activities for scientific meetings with internal and external stakeholders
  • Conducting transparency reporting on a quarterly and ad-hoc basis for PPSA/EFPIA compliance
  • Tracking and managing external facing SharePoint sites, including set-up, maintenance, and managing user access and content management.
  • Uploading all required documents into the Client systems per applicable compliance requirements
  • Coordinating internal and external meeting management and draft/review agendas and minutes
  • Tracking project timelines and deliverables and follow-up on action items
  • Troubleshoot issues as they arise and work to bring to timely resolution
  • Adherence with all applicable compliance requirements
  • Assist with ad-hoc requests in CORE, which may include formatting documents, creating job aids/checklists, and developing training guides/presentations.
Required Experience and Skills:
  • Exposure to clinical/observational research (1-3 years of related job or equivalent experience; e.g. Research Assistant, Research Coordinator, and/or Project Manager)
  • Proficient and knowledgeable in Microsoft 365 applications (Word, Power Point, Excel, Teams, etc.)
  • Must have strong communication and organizational skills
  • Strong project management skills
  • Ability to be flexible and manage multiple deadlines simultaneously
  • Ability to work independently
  • Basic knowledge of epidemiologic or outcomes research
Education:
  • Bachelor's degree in public health (or closely related discipline: epidemiology, biostatistics, biometry, or biological sciences) required
  • Master's degree a plus but not required


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Many Thanks,   

Sree Kanth
Recruitment Manager
Sree@newageclinical.com

NewAgeSys, Inc.
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