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ACL Digital is seeking an Associate Director of Medical Publications for a remote, contract role (6–12 months) in the Cell Therapy space. You will lead publication execution across manuscripts, abstracts, posters, and presentations, coordinating with stakeholders to ensure timely, quality outputs.
The role requires an advanced life sciences degree and 5–7+ years of medical publications experience, with strict adherence to ICMJE and GPP guidelines and the ability to operate with minimal
Job Title: Associate Director Medical Publications
Duration: 6–12 months, potential extension
Location: Remote
Therapeutic area: Cell Therapy
The Publications Lead (Contractor) supports the delivery of scientific publications across one or more therapeutic areas during a high-priority period. This role works alongside existing Publications Leads to provide additional leadership, executional support, and flexibility across the portfolio.
The position is suited for an experienced publications professional who can quickly embed within the team, independently manage key deliverables, and flex across priorities as needed to ensure timely, high-quality scientific communication.
Partner with existing Publications Leads to support delivery of publication plans across priority programs
Step in to lead specific publications, workstreams, or assets as needed
Provide additional bandwidth during peak periods (e.g., congress timelines, key data readouts)
Lead development and execution of manuscripts, abstracts, posters, and presentations
Manage publication lifecycle from planning through submission and post-publication activities
Ensure timely delivery of high-quality outputs aligned with agreed timelines
Track publication milestones and maintain publication trackers and calendars
Work closely with Medical Affairs, Clinical, HEOR, and other stakeholders to ensure alignment
Interface with authors, investigators, and external experts
Support publication planning discussions and decision-making as needed
Provide direction to medical writing agencies and review deliverables for scientific quality
Manage timelines, risks, and competing priorities across multiple deliverables
Ensure efficient execution across internal teams and external partners
Ensure all publications adhere to ICMJE, GPP, and internal policies
Maintain scientific rigor and accuracy across all outputs
Support audit-ready documentation and adherence to publication processes
Flex across therapeutic areas, assets, or deliverables based on evolving business needs
Pick up in-flight projects or support areas requiring additional focus
Help maintain continuity and momentum across publication activities
Advanced degree (PhD, PharmD, MD, or MSc) in life sciences
5-7+ years of experience in medical publications within pharma/biotech
Strong knowledge of publication guidelines (ICMJE, GPP)
Ability to operate independently with minimal onboarding
Strong prioritization and ability to manage parallel workstreams
Comfortable stepping into partially developed projects
Clear, pragmatic communication with stakeholders in a compliance-driven environment
Strong quality mindset and attention to detail