Position title
Remote jobs san diego
Employment Type
Base Salary
USD20-USD35 Per hour
Job Location
United States
Remote work from: USA

*IRT - Interactive response technologies

*Pharma or Biotech or supplier experience required

*Must have experience designing or maintaining IRT systems for clinical trials

*Candidate will be working remote - open to US Time Zone

The Manager, Clinical Systems (IRT) will work with a cross-functional team of internal stakeholders (including but not limited to: Clinical Study Management, Supply Chain and Data Management functions) and technology suppliers to support the implementation and maintenance of interactive response technology (IRT) solutions to support a clinical trial. The Manager, Clinical Systems (IRT) will provide technical oversight to ensure that IRT solutions adhere to the study protocol, industry regulations / best practices as well as company policies, procedures and guidelines.


  • 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

Basic Qualifications:

  • Doctorate Degree


  • Master's Degree and 3 years of IRT experience


  • Bachelor's Degree and 5 years of IRT experience


  • Associate's degree and 10 years of IRT experience


  • High school diploma/GED and 12 years of IRT experience

Preferred Qualifications:

  • 5+ years of IRT experience
  • Bachelor’s Degree in life science, computer science, engineering, business or related discipline
  • 4+ years of experience in clinical operations, clinical supply chain or clinical systems management
  • Experience implementing clinical systems, such as IRT and eCOA
  • Working knowledge of Good Clinical Practices and FDA regulations governing clinical trial execution
  • Detail-oriented and able to manage many projects simultaneously
  • Excellent documentation and communication skills
  • Meeting management and facilitation skills
  • Vendor management experience
  • Excellent time management and organization skills in a timeline-driven environment
  • Sound problem resolution, judgment, and decision-making abilities
  • Work well in a team-based environment with minimal supervision

Why is the Position Open?

Back fill for another external worker who recently moved into a new position

Top 3 Must Have Skill Sets:

Negotiation with external vendors, management of projects and people, familiarity with documentation in a regulated environment

Employee Value Proposition:

Long term contract with the possibility of extending beyond and there is always the possibility of converting to permanent down the road.

Possible Extension:Yes

Date posted
10 February 2024
Valid through
13 February 2025
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