“This Company requires all staff, staff augmentation external workers, and certain other external workers, in the United States and puerto rico vaccinated from COVID 19 as a condition of assignment at this company. In accordance with applicable law, this company will provide reasonable accommodations staff augmentation external workers qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance. Such accommodation may not pose an undue hardship this company, its operations, or its staff.”                                                        

Top 3 Must Have Skills        

• Pharma or Biotech or supplier experience required
• Must have experience designing or maintaining IRT (Interactive Response Technology) systems for clinical trials
• Negotiation with external vendors, management of projects and people, familiarity with documentation in a regulated environment

Day to Day Responsibilities:    

• Serve as the champion and consultant for most efficient and effective IRT design as needed per study protocol
• Lead and facilitate system requirements gathering meetings with clinical study teams and IRT supplier contacts
• Design and oversee the development of study-specific IRT technical documents
• Document issues and risks, and implement mitigation plans in partnership with study team and technology supplier PM
• Identify and track study-related technical issues to resolution
• Closely manage project-related timelines and associated activities

"This posting is for Contingent Worker, not an FTE"