What are the responsibilities and job description for the Principal Regulatory Strategist (CRO/Pharma Industry) - Remote position at MMS?
Job Description
Job Description
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
This would be a full-time consultancy role, working remotely.
Principal Regulatory Strategist
Responsibilities
- Provide consulting and advisory services for complex regulatory issues or projects.
- Author and maintain documentation as required to sustain regulatory compliance.
- Provide senior technical review for complex regulatory projects.
- Conduct regulatory intelligence gathering to support development of regulatory roadmaps, complex feasibility assessments, and other regulatory intelligence reports.
- Participate on project teams and provide expertise on related regulatory matters.
- Clearly and accurately conveys information to peers, supervisors, and other stakeholders.
- Participates in in implementation of new / updated operational strategies to comply with new / updated policies and recommendations.
- Identifies new / updated policies and recommendations and may provide professional opinions on impact of regulatory changes to MMS and Clients (from the desk of, blogs, webinars, etc.).
Requirements
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