Regulatory Affairs Project Manager

Work Location : Open to both Rahway, NJ / Upper Gwynedd, PA

Type : Hybrid( flexible days)

Education :

Minimum BS Degree preferably in technical, business or science.

Required Experience :

At least 12 years in the pharmaceutical industry with at least 5 years in Regulatory / Pharmacovigilance Function or Alliance or Business Development.

Ability to influence and effectively operate in an ambiguous / rapidly changing environment while being quality and compliance oriented.

Proven and demonstrated skills in project management and leadership, strategic, proactive, and a creative problem-solver that generates options and drive results in a deadline driven environment.

Strong virtual and in person collaboration

Demonstrated facilitation and leadership skills.

Clear communicator and goal oriented.

Comfort and experience building and presenting effective slide presentations with audiences at all levels of the organization.

Independent thinker and worker.

Highly organized, motivated, and detail-oriented while still able to keep overall "big picture" view of projects and strategies.

Demonstrated analytical and data management skills. Experience pulling together abstract milestones and data into centralized management report.

Demonstrated ability to lead cross functional teams and facilitate cross functional meeting to achieve a purpose.

Strong, demonstrated project management capabilities and skills.

Ability to collaborate and manage multiple projects at various stages of the process simultaneously.

Ability to communicate messages in a clear and concise manner both verbally and in writing.

Experience with change management concepts and execution.

Strong proficiency with generating content using all MS Office tools including but not limited to Word, Excel, Power-Point and SharePoint.

Some experience creating and modifying MS Teams and MS Project or related tools to manage project timelines and collaboration.