What are the responsibilities and job description for the Director, Medical Writing Job at MindMed in Durham position at MindMed?
MindMed is a clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. Our mission is to be the global leader in the development and delivery of treatments that unlock new opportunities to improve patient outcomes. We are developing a pipeline of innovative product candidates, with and without acute perceptual effects, targeting neurotransmitter pathways that play key roles in brain health.
Founded in 2019, we are continuously expanding our presence and global footprint. We are constantly searching for high-impact individuals in various clinical, technical and business operations domains to strengthen our team of patient-centric, intelligent individuals.
Responsibilities
- Authors routine clinical and regulatory documents (e.g., clinical study protocols, clinical study reports, and investigator's brochures, and sections of regulatory submissions) in partnership with cross-functional team with oversight
- Supports clinical study execution through expert review of study-level documents authored by other functions (e.g., study deviations, analysis plans, data outputs)
- Coordinate and lead document roundtables, reviews, approvals, quality control (QC) and other document content issues and overall questions during the authoring process
- Develops timelines for documents and communicates with team members to maintain awareness of expectations, milestones, and deliverables
- Collaborates with cross-functional team to review study results
- Contributes scientific knowledge and analytical skills to the production of documents
- Participates in developing key messages for routine documents and conduct literature searches
- Reviews clinical trial registry postings for assigned studies
- Review and update style guide to ensure consistency across documents
- Stay current with respect to key global guidance documents, regulations, or directives
- Works effectively with an electronic document management system and related tools to develop clinical documents
- Maintain effective working relationships with contractors, vendors and partners
Requirements
The starting base pay range for this position is $184,402.00 - $215,190.00. Compensation will be determined based on several factors including, but not limited to, skill set, years of experience, and the employee's geographic location.
Employees in this role may be entitled to additional compensation, including bonus and equity. Benefits information is listed on our Jobs Page. The Company provides competitive benefits to employees including :
J-18808-Ljbffr
Salary : $184,402 - $215,190