Syner-G
The MWS Consultant I plays a critical role in authoring and managing regulatory documents, supporting client regulatory strategies, and ensuring high-quality deliverables that align with client expectations and regulatory standards. This role is responsible for leading document development efforts, coordinating regulatory projects, and collaborating with cross-functional teams to meet diverse client needs across varying stages of development. The MWS Consultant serves as both a technical contributor and project owner, ensuring document accuracy, submission readiness, and adherence to regulatory requirements while maintaining strong client relationships and delivery excellence.
Headquarters
Framingham, Massachusetts, United States
Company Size
201-500 employees
Founded
2007
Syner-G is a strategic development and delivery partner for biopharma innovators, focused on turning scientific breakthroughs into real-world therapies faster, smarter, and with greater impact. They provide integrated development and delivery support to help biotech and pharma teams advance programs from concept toward the clinic. By combining strategic planning, operational execution, and cross‑functional expertise, Syner-G aims to de‑risk programs, accelerate timelines, and maximize patient impact.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Syner-G.
Syner-G didn’t post a salary, so this is our estimate from similar listings.
Associate Director, Regulatory Affairs Europe
Acadia Pharmaceuticals Inc.
Forward-Deployed Regulatory Affairs/Medical Writer
Edison Scientific
PLS - Remote (MN); PLS - Remote (MD); PLS - Remote (OH); PLS - Remote (MA); PLS - Remote (IL); PLS - Remote (NC)
Pace® Analytical Services
Program Manager, Regulatory Medical Writing - Client-dedicated FSP
lifelancer
Director Medical Writing Asset Lead
GSK plc
Director, Regulatory Strategist, GRS
Bristol Myers Squibb