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Sage Therapeutics Associate Director, Medical Writing in EMAIL:, Massachusetts

General Scope and Summary

SAGE Therapeutics is searching for a creative, resourceful, integrative thinker for an important role that is responsible for planning and preparing clinical and regulatory documents (protocol, CSR, IB, clinical sections clinical trial and marketing authorization applications, periodic annual reports, etc.) according to company guidelines and international governmental regulations. The Associate Director, Medical Writing is responsible for presenting clinical data objectively in a clear, concise format, and also for organizing and managing the reviews for these documents. This position will have a role in the leadership of the department, and in overseeing/managing medical writing vendors, contract staff, and/or junior medical writers. The Associate Director, Medical Writing will function under the guidance and direction of the head of the medical writing department. The successful candidate will be an independent, proactive, experienced medical writer with experience working in a clinical development environment.

Roles and Responsibilities

  • Works with colleagues from various functional areas in Clinical Development, Clinical Operations, Medical Science, Medical Affairs, Regulatory, and Program Management in planning and preparation of high quality clinical and regulatory documents, including protocols, study reports, investigator brochures, etc., according to company and agency guidelines in order to support drug development under strict timelines.

  • Independently writes as well as oversees and manages the work of other medical writers. This includes training and mentoring in addition to participation in assessing workload and managing work assignments.

  • Contributes to and/or manages the production of relevant documentation for regulatory submissions.

  • Proactively and independently works to ensure continuous improvement, and high standards for quality and productiveness; provide suggestions based on area of expertise and prior experience.

  • Leads the Medical Writing team in designing and maintaining templates/standards for protocols/reports in accordance with ICH guidelines and medical writing best practices.

  • Provides leadership in area of expertise.

  • Has a working knowledge of the company‚Äôs financial goals and metrics.

  • Collaborates with department management on the departmental budget and planning; authorize payment of work on projects and accountable to ensure successful completion and payment of work.

  • Suggests direction and strategic ideas within area of expertise.

  • Provides managerial leadership in area of expertise.

Experience, Education and Specialized Knowledge and Skills

Must thrive working in a fast-paced, innovative environment while remaining flexible, proactive, resourceful and efficient. Excellent interpersonal skills, ability to develop important relationships with key stakeholders, good conflict management and negotiation skills, ability to analyze complex issues to develop relevant and realistic plans, programs and recommendations. Demonstrated ability to translate strategy into action; excellent analytical skills and an ability to communicate complex issues in a simple way and to orchestrate plans to resolve issues and mitigate risks.

Basic Qualifications

  • MS or equivalent in a biological science with 7+ (or BS with 10+) years of medical writing experience in the pharmaceutical industry; specific experience in neuroscience, psychiatry, or related field is ideal.

Preferred Qualifications

  • Expertise in drug development, clinical research, medical terminology, study design, and the regulatory requirements for clinical and regulatory documents.

  • Keen understanding of the requirements for preparation of key clinical and regulatory documents.

  • Experience working with all levels of management and consulting with key business stakeholders.

  • An ability to influence for greater outcomes.

  • Strong team player that has a customer service approach and is solution oriented.

  • Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors.

  • Possesses strong written and verbal communication skills.

  • Embrace our core values: Put People First, Do Big, Be Accountable, Grow through Learning and Change, and Work Fun. Excitement about the vision and mission of Sage

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#Biotechnology #Careers #ThisIsSage

All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.

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We value our relationships with professional recruitment firms. To protect the interests of all parties, and given the large volume of inquiries received from third-party placement agencies, we are not able to respond to all agency inquiries. We do not accept unsolicited resumes from any source other than directly from candidates for current or future positions. Submission of unsolicited resumes in advance of a signed agreement between our company and a placement agency does not create an implied obligation and, if an unsolicited candidate represented by a placement agency is hired, we are not obligated to pay a fee. Only approved recruitment firms will be allowed to provide services to Sage Therapeutics, Inc.

Protected personal characteristics include: age, race, ancestry, color, sex, national origin, sexual orientation, gender identity or expression, religious creed, mental or physical disability, pregnancy, genetic information, marital or civil union status, participation in the uniformed services of the United States, or any other characteristic protected under applicable federal, state or local law. To learn more, see Sage's Anti-Harassment and Equal Opportunity Policy