What are the responsibilities and job description for the Regulatory Affairs Project Manager position at Omiz Staffing Solutions (OSS)?
Hiring a Regulatory Project Manager (RPM) in Foster City, CA🚀
Are you ready to make a difference in the biopharma industry? One of our Biopharmaceutical customers is seeking a Regulatory Project Manager (RPM) to join their team and play a critical role in advancing regulatory initiatives. This is a fantastic opportunity to work in a dynamic, cross-functional environment and contribute to innovative solutions in drug development.
Location : Foster City, CA (Hybrid)
Duration : 9 months (with potential for extension)
Pay Rate : $65 – $74 / hour (W2)
What You’ll Do :
Manage cross-functional programs and project communications to keep stakeholders informed and aligned.
Provide project management support for regulatory activities, including timelines, action items, and deliverables.
Foster collaboration across Regulatory Affairs groups, including Labeling, Regulatory CMC, Medical Writing, and more.
Track, prepare, and support regulatory submissions for INDs and RTQs.
Collaborate with senior project managers to execute on deliverables and optimize processes.
Contribute to operational tasks while developing a strategic mindset.
What You’ll Bring :
Education & Experience :
- BA / BS 5 years of relevant project management or scientific experience in the biopharma industry OR 3 years with an advanced degree.
- Scientific background preferred.
- PMP certification or equivalent is a plus!
Knowledge & Skills :
Why Join Us?
We are committed to creating a culture of trust, collaboration, and excellence. This role offers a unique opportunity to support groundbreaking regulatory projects and make an impact in patients' lives.
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Salary : $65 - $74
