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CSPV Project Manager II

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The Fountain Group LLC

2024-10-04 17:49:09

Job location Basking Ridge, New Jersey, United States

Job type: fulltime

Job industry: I.T. & Communications

Job description

Details for the position are as follows:

Location: Remote, with a preference for EST-based candidates. Candidates local to Basking Ridge, NJ who can come onsite once a week are also preferred.

Pay: $60.72 - $67.86 per hour

6-month contract to start with the strong possibility of extension depending on performance.

Job Description:

We are seeking an experienced IRT Project Manager with expertise in managing Interactive Response Technology (IRT)-related activities across multiple clinical trials. This role involves leading cross-functional teams and collaborating with global stakeholders from Europe and Japan. The successful candidate will support key initiatives across Clinical Safety and Pharmacovigilance (CSPV) while driving business excellence and PMO structures within the organization.

Lead cross-functional teams in project management and execution for key initiatives across CSPV.

Manage IRT-related activities across multiple clinical trials, ensuring compliance with Good Clinical Practices (GCP), Good Manufacturing Practices (GMP), and Daiichi Sankyo standards.

Serve as the subject matter expert (SME) for IRT systems, driving the development and delivery of IRT solutions across global matrixed teams.

Support the Management Office and Business Excellence Lead in implementing PMO structures within CSPV.

Collaborate with CSPV leadership to support the globalization of CSPV through business excellence activities.

Oversee project management tasks, including stakeholder alignment, objective setting, timeline tracking, issue resolution, and outcome achievement.

Generate and report status updates to leadership while managing communication plans for key stakeholders.

Facilitate global, cross-functional discussions to identify and resolve risks, issues, and dependencies.

Required Skills:

Bachelor's degree required.

Minimum of 4 years of experience as a subject matter expert (SME) in IRT for clinical trials.

Strong project management and leadership abilities.

Expertise in IRT systems and clinical trial processes.

Proficiency in generating reports and tracking project milestones and deliverables.

Ability to identify and mitigate risks and dependencies in global projects.

Inform a friend!

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