Clinical Systems Leader

Only local San Francisco Bay Area candidates!

No 3rd party agencies. Direct W2 contractors only!

The Clinical Systems Leader (CSL) is responsible for implementing all related clinical systems actions
used in the development of clinical trials within Early Clinical Development (ECD). The CSL collaborates
with a cross-functional team of internal stakeholders and technology vendors to ensure the successful
implementation and maintenance of technology solutions supporting clinical trials.

Primary Responsibilities:
Study Execution and System Management: Accountable for implementing all related clinical
systems, such as Interactive Response Technologies (IxRS) and electronic Clinical Outcome
Assessments (eCOA) actions for the ECD portfolio.

Project Management: Closely manage study-related timelines and associated activities. Manage
and lead the end-to-end specifications for the build of clinical systems for an assigned study or
enterprise project. This includes requirements review, testing, deployment, maintenance,
enhancement, and closeout.

Technical Oversight: Provide technical oversight to ensure that clinical systems solutions (e.g.,
IxRS/eCOA) adhere to the study protocol, industry regulations/best practices, and company
policies, procedures, and guidelines.

Collaboration and Teamwork: Work with a cross-functional team of internal stakeholders
(including but not limited to: Clinical Trial Leader, Biostatistician, Drug Supply Chain, Data
Management functions, and Procurement) and technology vendors. Work independently with PET
stakeholders and/or cross-functional project teams with little to no oversight. Works
collaboratively with the ECD I&A team to share knowledge.

Issue and Risk Management: Proactively identify and track study-level technical issues to
resolution. Ensure prompt resolution of system issues, document issues and risks, and
implement mitigation plans in partnership with the study team and technology vendor project
manager.

Communication & Presentation Skills: Strong verbal and written communication skills; strong
business presentation skills; Able to explain technical issues and communicate clearly, concisely,
and professionally with internal, external stakeholders and departmental leadership.

Skills required:

Bachelor's Degree in life science, computer science, engineering, information system, data
science or related discipline
2-5 years of experience in Clinical Operations, or Clinical Systems Management
2-5 years of IxRS/IRT and clinical-related systems experience
Successful track records in leading the implementation of clinical systems, such
as IxRS/IRT, ePRO, and eCOA
Working knowledge of Good Clinical Practices and FDA regulations governing
clinical trial execution
Excellent written and verbal communication skills and strong project
management skills
Familiar with documentation in a regulated environment. Experience in Veeva is a
plus