Consultant I, Medical Writing

POSITION OVERVIEW:

The MWS Consultant 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.

WORK LOCATION:

Work location may vary based on client needs and project requirements. Travel may be required to client sites or Syner‑G offices depending on engagement expectations.

KEY RESPONSIBILITIES:

(This list is not exhaustive and may be supplemented or changed as necessary.)

• Author a variety of regulatory documents including Clinical Study Reports (CSRs), study protocols, and client submission materials.
• Lead the development of complex regulatory modules such as Module 2 summaries, Briefing Documents, and Orphan Drug, Fast Track, and Breakthrough Designation applications.
• Ensure consistency, accuracy, and alignment across documents with client updates and applicable regulatory standards.
• Apply quality control and submission‑readiness processes to deliver high‑quality documents within agreed client timelines.
• Serve as a project owner by tracking timelines, adjusting schedules, and coordinating with clients to address evolving project demands.
• Plan for and anticipate project challenges, update visual timelines, and maintain adherence to deadlines.
• Facilitate client interactions including meetings, inquiries, and feedback discussions while building and maintaining client trust.
• Support early‑stage and smaller clients by contributing to regulatory strategy development.
• Collaborate with cross‑functional teams to ensure the quality and accuracy of regulatory deliverables.
• Provide guidance on tools, document management systems, and client SOPs.
• Engage in continuous learning through exposure to new document types, processes, and industry best practices under senior mentorship.

QUALIFICATIONS AND REQUIREMENTS:

Education:

• Advanced degree in a life or health science discipline (e.g., M.S., PharmD, Ph.D., or M.D.) preferred.
• RAC certification beneficial.

Experience & Core Competencies:

• Strong foundation in medical writing, regulatory writing, and interpretation of scientific content.
• Ability to communicate complex scientific and regulatory information clearly and concisely, both in writing and verbally.
• Exceptional project and time management skills with the ability to manage multiple priorities and proactively adjust timelines.
• Strong critical thinking and data analysis skills to ensure scientific claims align with supporting evidence and regulatory expectations.
• High attention to detail with the ability to ensure consistency and accuracy across multiple document reviews.
• Patient and empathetic approach, particularly in cross‑cultural and client‑facing environments.
• Positive attitude toward feedback and continuous improvement.

Technical Skills:

• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), Microsoft Teams, and MS Project.
• Familiarity with regulatory document management systems such as Veeva Vault.
• Knowledge of pharmaceutical and biopharmaceutical environments, including clinical trials and regulatory submissions.
• Experience with regulatory submissions and an understanding of global regulatory standards.

ESSENTIAL FUNCTIONS: 

Physical Demands: 

The physical demands described here are representative of the requirements that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 

While performing the duties of this job, the employee is regularly required to use a computer keyboard and mouse; reach with hands and arms; talk and listen. The employee is frequently required to walk and sit, as well as to lift and carry objects such as books and files weighing up to 25 pounds. The employee is occasionally required to stand, stoop, or kneel. Specific vision abilities required by this position include close vision and the ability to adjust focus. 

Work Environment: 

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job, including moderate noise level, an indoor temperate environment, and light levels that are bright and conducive to minimal eye strain, typical for an office environment. 

TOTAL REWARDS PROGRAM:

We define total rewards as compensation, benefits, remote work/flexibility, development, recognition and our culture with programs that support each of our reward pillars.  This includes a market competitive base salary and annual incentive plan, robust benefit offerings, and ongoing recognition and career development opportunities. Employees also enjoy our generous flexible paid time off program, company paid holidays, flexible working hours, and fully remote or hybrid work options for some roles.  However, if a physical work location is more for you, we have office locations in Greater Boston; San Diego, CA; Boulder, CO; and India.  Additionally, our Technical Operations team regularly work at physical client sites.

Currently, Syner-G is unable to sponsor or take over sponsorship of an employment Visa at this time.