Associate Director, Medical Writing Technology and - Dedham, United States - Synterex

Synterex

Verified Company

Dedham, United States

3 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

Synterex, Inc.

is a consortium of highly experienced clinical development professionals specializing in medical writing, submission publishing, and clinical science and operations support.

Synterex offers remote or on-site services, with a focus on providing clear, concise, accurate, and fully compliant documentation, from early drug development through post-approval.

Location:
Fully remote position, but must be able to attend key meetings on site with clients as requested.

Essential Duties & Responsibilities

Spearhead the development and integration of technology solutions in medical writing, including AIbased tools, natural language processing, and structured content authoring
Collaborate with internal and client teams to identify and build user cases and intentions that improve content architecture and delivery; develop and execute on the product roadmap on time and within budget
Lead projects using agile and other project management methodologies to ensure timely and successful implementation of software development initiatives
Navigate legal, intellectual property, and data privacy and security concerns associated with integrating AI and technology in medical writing
Evaluate and document the business impact and return on investment of technology initiatives for clients and stakeholders
Foster a culture of continuous learning and innovation within the medical writing team, providing guidance on best practices in technology and content architecture.
Drive the attraction and retention of top talent and help develop trainings and presentations to create buyin for AI and the evolving role of the medical writer
Oversee the work of junior writers contributing to technologydriven medical writing initiatives
Enhance Synterex presence with relevant professional organizations

Requirements:

Experience (8+ years) as a medical writer in the CRO/biotech/pharmaceutical field, or equivalent
Advanced degree in a relevant field (ie, Life Sciences, Data Science, Computer Science) required.
Expertise in global guidelines and regulations for drug development, including ICH GxP and US/exUS regulatory requirements
Expertise with document management systems
Ability to work both independently and collaboratively in the face of competing priorities
Serviceoriented and proactive approach to project management and familiarity with project management methodologies, including agile
Excellent conflict management and negotiation skills
Strong written and verbal communication skills

Track record of outstanding leadership and mentorship in the medical writing and quality assurance fieldsSynterex provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.