Clinical Regulatory Affairs Project Leader

2 weeks ago


Deerfield Beach, Florida, United States Rose International Full time

Position Overview:

The Project Manager for Quality Clinical Regulatory Affairs is responsible for leading critical compliance initiatives that span multiple business units and functions globally. This role demands a strong onsite presence and is tailored for candidates located in the Deerfield, IL area.

Key Qualifications:

  • A minimum of a Bachelor's degree or equivalent in Operations or a related field, accompanied by at least 3 years of project management experience.
  • Proven experience in a regulated sector such as pharmaceuticals or medical device manufacturing, with a solid understanding of GMP regulations.
  • PMP (Project Management Professional) Certification is highly desirable.
  • Demonstrated self-motivation, teamwork, and excellent interpersonal skills, with a track record of leading high-performing teams.
  • Exceptional leadership capabilities.
  • Proficiency in Microsoft Project, Excel, and PowerPoint.
  • Ability to navigate a virtual environment with diverse teams across various time zones.

Responsibilities:

  • Provide strategic project planning and leadership, aligning with the overall program objectives.
  • Offer clear guidance on requirements to meet the expectations of internal stakeholders.
  • Engage with all organizational levels to ensure effective communication regarding priorities and progress updates.
  • Accountable for the performance of core teams and the execution of program schedules.
  • Monitor capital projects related to the program, escalating any delays or risks as necessary.
  • Identify and communicate project risks, developing proactive management strategies.
  • Anticipate potential conflicts and manage them to achieve mutually beneficial outcomes.
  • Drive continuous improvement in the organization’s ability to execute programs from inception to implementation.
  • Adhere to project management guidelines, performance metrics, and regulatory standards to apply best practices in project management.

Important Notes:

  • Only candidates authorized to work in the designated country will be considered.
  • All position start dates and durations are estimates and may vary based on business needs.

Equal Opportunity Employer:

Rose International is committed to providing equal employment opportunities. All qualified applicants will be considered without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other characteristic protected by law.

If assistance is needed during the application process, please reach out to our HR Department.



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