What are the responsibilities and job description for the Regulatory Affairs Project Manager Professional position at Intelliswift - An LTTS Company?
Job Description:
We are seeking a highly skilled Regulatory Affairs Project Manager to join our team at Intelliswift - An LTTS Company. In this role, you will be responsible for managing projects related to regulatory affairs and ensuring compliance with industry regulations.
About the Role:
This is a hybrid position, allowing for flexible days in either Rahway, NJ or Upper Gwynedd, PA. You will have the opportunity to work on a wide range of projects, from project management and leadership to strategic planning and problem-solving.
Key Responsibilities:
Requirements:
To be successful in this role, you will need:
Benefits:
We offer a competitive salary and a comprehensive benefits package, including health insurance, retirement savings, and paid time off.
We are seeking a highly skilled Regulatory Affairs Project Manager to join our team at Intelliswift - An LTTS Company. In this role, you will be responsible for managing projects related to regulatory affairs and ensuring compliance with industry regulations.
About the Role:
This is a hybrid position, allowing for flexible days in either Rahway, NJ or Upper Gwynedd, PA. You will have the opportunity to work on a wide range of projects, from project management and leadership to strategic planning and problem-solving.
Key Responsibilities:
- Manage projects related to regulatory affairs, including pharmacovigilance and alliance development
- Develop and implement strategies for influencing and operating in an ambiguous/rapidly changing environment
- Lead cross-functional teams and facilitate meetings to achieve project goals
- Communicate effectively with stakeholders at all levels of the organization
- Maintain quality and compliance oriented approach
Requirements:
To be successful in this role, you will need:
- A minimum BS degree in technical, business, or science
- At least 12 years of experience in the pharmaceutical industry, with 5 years in regulatory/pharmacovigilance or alliance/business development
- Proven project management and leadership skills
- Ability to collaborate and manage multiple projects simultaneously
- Strong analytical and data management skills
- Experience with MS Office tools and project management software
Benefits:
We offer a competitive salary and a comprehensive benefits package, including health insurance, retirement savings, and paid time off.
