We're looking for a Regulatory International Project Manager, working in the Biotechnology/Medical Devices industry in San Rafael, California, United States.
Manages regulatory international operations including scheduling and facilitating meetings with the international and global regulatory team members.
Monitors submission and preparation progress to ensure timely filing to health authorities.
Documents project milestones, deliverables and reports progress against team, department, and corporate goals.
We are offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Bachelors degree required
3 years of project management experience
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.