Syner-G
ConsultantI,MedicalWriting
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Consultant I, Medical Writing at Syner-G. Skills: Medical writing, Regulatory writing, Document management, Client relations. Author regulatory documents. Lead development of complex modules”
What You'll Achieve.
Deliver high-quality documents; Meet client timelines; Address evolving client demands; Maintain adherence to deadlines; Build client trust; Maintain client trust; Ensure document consistency; Ensure document accuracy; Ensure document alignment
Industry & Context.
Critical thinking; Data analysis
Lift and carry up to 25 pounds
What They're Looking For.
Must Have
3+ years industry experience, Proficiency in Microsoft Office Suite, Proficiency in Teams, Proficiency in MS Project, Familiarity with regulatory document management systems, Experience with regulatory submissions, Understanding of global regulatory standards, Foundation in medical writing, Foundation in regulatory writing, Foundation in interpretation of scientific content, Knowledge of pharmaceutical environments, Knowledge of biopharmaceutical environments, Knowledge of clinical trials, Knowledge of regulatory submissions, Effective written communication skills, Effective verbal communication skills, Ability to communicate complex scientific information, Ability to communicate complex regulatory information, Exceptional project management skills, Exceptional time management skills, Ability to prioritize multiple projects, Ability to adjust timelines proactively, Critical thinking skills, Data analysis skills, High attention to detail
Nice to Have
Advanced degree in life or health science, RAC certification is beneficial
What You'll Do.
Author regulatory documents
Lead development of complex modules
Apply quality control processes
Apply submission-readiness processes
Deliver high-quality documents
Track project timelines
Adjust project schedules
Coordinate with clients
Address evolving demands
Plan for project challenges
Update visual timelines
Maintain adherence to deadlines
Facilitate client interactions
Address client inquiries
Discuss client feedback
Maintain client trust
Ensure document consistency
Ensure document accuracy
Ensure document alignment
Contribute to regulatory strategies
Provide guidance on tools
Provide guidance on document management systems
Provide guidance on client SOPs
Engage in continuous learning
Expose to new document types
Expose to new processes
Expose to industry best practices
How You'll Work.
Team & Collaboration
Cross-functional teams
Communication Scope
Written communication; Verbal communication; Scientific communication; Regulatory communication; Client communication
Process & Methodology
Timeline tracking, Schedule adjustment, Deadline adherence
Full Job Description
COMPANY DESCRIPTION: A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science and delivery of life-enhancing therapies to more patients. We work across a diverse range of clients and projects, supporting many organizations from the most critical phases of the drug discovery and approval process through to commercialization. It is meaningful, varied and thought-provoking work with a strategic emphasis, a solutions-driven approach and significant, real-world outcomes, from science to delivery/success. To learn more about who we are and what drives us, watch our company video here. Underpinning this mission is a culture that aligns perfectly with what we want to achieve. We enable our people to grow, we support them in their learning and we reward them in so many different ways. In return, they play an instrumental role in maintaining our reputation across the globe as a strategic biopharma product development and delivery partner. Syner-G was recently honored with BioSpace's prestigious "Best Places to Work" 2026 award, for the third consecutive year, along with many other award-winning programs to make a career here truly life-enhancing. These recognitions are a testament to our commitment to fostering a positive and engaging work environment for our employees, with a particular emphasis on culture, career growth and development opportunities, financial rewards, leadership and innovation. At Syner-G, we recognize that our team members are our most valuable asset. Join us in shaping the future, where your talents are valued, and your contributions make a meaningful impact. For more information, visit www.Synergbiopharma.com POSITION OVERVIEW: The MWS Consultant I plays a critical role in authoring and managing regulatory documents, supporting client regulatory strategies, and ensuring high-quali
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