Director / Senior Director, Marketing Operations
Cogent Biosciences
Vault
Job Level
Mid-LevelSenior
Tech Stack
Vault
About the role
- Support Manager, Medical Content Development on content development-related engagements for commercialization deals and medical information/medical affairs consulting
- Write and create medical/scientific content: SRDs, FAQs, slide sets, abstracts, posters, education/training materials, etc
- Drive client document development process from gathering materials to facilitating MLR review meetings
- Work with document management platforms (Veeva PromoMats / MedComms) as content owner when appropriate
- Perform scientific data fact checking for documents supporting medical reviewers
- Collaborate on strategy, tactical execution and communication approaches; participate in client meetings
- Support thought leadership content: articles, newsletters, publications, congress presentations, slides, blogs
- Create/update SOPs, checklists, templates, style guides, and guidance documents
- Mentor and coach team members; support hiring and onboarding
- Stay knowledgeable of industry best practices and support implementing new technologies/procedures
- Work collaboratively with other medical writers and creative teams; other duties as assigned
Requirements
- PharmD (or M. Pharm. or M.S. Pharm), PhD, or MD with medical writing and content development experience
- Minimum of 4 years of experience within the life science and/or pharmaceutical industry with extensive medical writing and content development experience
- Direct Medical Information / Medical Communications / Scientific Communications experience
- Exceptional communication skills including, written, oral, interpersonal, and presentation skills
- Ability to effectively interface with all levels of management and staff and to succeed in a matrix team setting while meeting or exceeding timelines
- Familiarity with AMA Style guide as well as an understanding of clinical research principles and applied statistics
- Familiarity with ICMJE, GPP, PRISMA, STROBE, CONSORT, etc.
- Proficient editing skills along with expertise in Microsoft Office, Acrobat and other applications
- Experience conducting literature searches and working with tools such as PubMed, Ovid, Embase, etc
- Experience working with reference management and citation software (e.g., EndNote, Mendeley, Citavi, etc.)
- Strong understanding of regulatory requirements and best practices in relationship to Medical Information, Medical Affairs and promotional and non-promotional materials review
- Excellent project management skills and proven track record of being results driven
- Ability to conceptualize, design and deliver best in class solutions
- Highly principled and collaborative
- Agile learning and ability to support and learn about multiple disease states and therapeutic areas
- Preferred: experience with Veeva Vault MedComms / Promomats; experience publishing abstracts, posters, manuscripts; experience developing medical content for new product launch
