Senior​/Manager, Medical Writing

Overview

The Opportunity: The Senior / Manager, Medical Writing is responsible for independently authoring and delivering high-quality routine clinical and regulatory documents and represents Medical Writing as a cross-functional team member for clinical study-level activities. This position will work directly with the Director, Medical Writing.

Your Role:

• Independently writing and delivering high-quality clinical and regulatory documents (e.g., clinical study protocols, clinical study reports, investigator’s brochures, integrated summaries, and sections of regulatory submissions) in partnership with internal cross-functional team members
• Coordinating effective document development, review, and approval
• Overseeing medical writing vendor writers for individual projects, as needed
• Actively contributing to development of processes and procedures to improve departmental and cross-functional workflows
• Building relationships and working collaboratively with study team members
• Reviewing study and program-level documents for clarity, accuracy, and consistency
• Developing in-depth study-level and program knowledge
• Contributing scientific knowledge and analytical skills to the production of documents
• Participating in developing key messages for clinical regulatory documents
• Developing document timelines and communicating with team members to maintain awareness of expectations, milestones, and deliverables
• Leading development of clinical trial registry postings for assigned studies
• Navigating an electronic document management system and related tools to develop clinical documents

• Bachelor's degree in relevant discipline required. PhD in molecular biology, genetics, or a related life sciences field preferred, (or equivalent degree).
• 3+ years of experience in the pharmaceutical/bi biotechnology industry as a medical writer
• Self-motivated and nimble with the ability to excel in a fast-paced environment
• Excellent written and verbal communication skills
• Strong interpersonal skills
• Experience producing high-quality scientific/medical documents
• Ability to analyze, interpret, and summarize clinical data
• Basic understanding of drug development, clinical research, study design, biostatistics, pharmacokinetics, regulatory requirements, and medical terminology
• Strong project management and organizational skills
• Initiative and creativity in solving routine problems for individual documents and in identifying process improvements within the Medical Writing department
• Attention to detail related to consistency, grammar, syntax, and scientific accuracy
• Proficiency in word processing, templates, table/figure creation, and literature searches

Estimated Salary Range: [$107,000 - $179,000]. The range provided above is based on what we believe to be a reasonable estimate for this job at the time of posting. Actual base salary will depend on a number of factors, including but not limited to, a candidate’s education, experience, skills and location.

About Relay Therapeutics:
Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients. Our Dynamo platform integrates leading-edge experimental and computational approaches to drug these targets. We have built a world-class team of leading experts and are driven by collaboration across the drug discovery process.

Our team is equal parts fearless and relentless, with a shared passion for working collaboratively in intellectually stimulating environments. If you’re excited by the challenge of putting protein motion at the heart of drug discovery and making a difference in the lives of patients, join us!

EEO statement:
Relay Therapeutics is an equal opportunity employer. We do not discriminate on the basis of any protected status. We welcome applicants from diverse backgrounds.