Senior Manager, Scientific Publications

Corcept Therapeutics•Redwood City, CA

About The Position

Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid receptor (GR). To date, we have discovered more than 1,000 selective proprietary cortisol modulators. In 2012, we received FDA approval of Korlym® (mifepristone), the first approved treatment for hypercortisolism (Cushing’s syndrome). Today, our team and collaborators continue to unlock the possibilities of cortisol modulation as a way to treat serious diseases. With more than 30 ongoing studies across a wide range of disease areas, including endocrinology, oncology, metabolism, and neurology, we remain dedicated to advancing the possibilities of cortisol modulation. What began as a ripple of scientific truth is now poised to unleash a sea change of discovery representing a fundamental shift in the way we understand and treat disease. The Senior Manager, Scientific Publications will provide expert scientific and medical writing support, focusing on publication strategy and execution for Clinical Development-led publications. Responsibilities include producing high-quality scientific abstracts, posters, presentations, and manuscripts, supporting the development of publication strategies, and collaborating on science-driven communication platforms.

Requirements

Proven ability to write, edit, and prepare scientific publications (abstracts, posters, presentations, and manuscripts) for diverse audiences including scientists, physicians, patients, payers, and others
Proven ability to work both independently and collaboratively in a fast-paced, cross-functional environment involving internal stakeholders and external scientific experts
Demonstrated agility in adapting to evolving business needs, priorities, and responsibilities while maintaining focus on key deliverables
Strong organizational skills with the ability to manage multiple complex projects simultaneously, even in ambiguous or shifting contexts
Advanced skills in data analysis, interpretation, synthesis, and scientific writing with exceptional attention to detail and editorial accuracy
Effective problem-solving, influencing, and negotiation skills to build productive working relationships across functions and with external thought leaders
Proficient with online literature searches using a variety of professional tools/databases
Advanced proficiency with EndNote (or equivalent), Microsoft Office Suite, Adobe Acrobat, publication submission platforms, document management systems (eg, Box, SharePoint) and publication tracking databases (e.g., PubsHub, Datavision)
Willingness to travel for conferences and professional meetings (~20%)
Advanced scientific degree (e.g. M.S., Ph.D., PharmD)
4+ years of related work experience in the pharmaceutical industry in medical affairs, publications, and/or medical communications
Knowledge of GPP 2022 and ICMJE industry guidelines (CMPP certification desired)
Applicants must be currently authorized to work in the United States on a full-time basis.

Nice To Haves

Experience in publication planning
Previous experience in endocrinology or metabolic diseases preferred
Experience with publication extenders and plain language summaries preferred but not required

Responsibilities

Manage the execution of therapeutic-area publication plans and contribute to publication plan updates
Write publications (including abstracts, posters, manuscripts, and presentations) that are scientifically accurate, relevant, and timely
Manage external vendors and agency partners, ensuring all deliverables are scientifically accurate, aligned with approved medical messaging, and meet quality, timeline, and compliance expectations
Maintain advanced therapeutic area and product expertise through proactive review and analysis of available and emerging scientific/clinical evidence
Collaborate, establish credibility, and build trust with internal strategy teams, program leads, and external PIs/KOLs
Ensure publications are developed, reviewed, and approved in compliance with corporate policies and industry guidelines (e.g. ICMJE, GPP 2022) and be accountable for timeline development and database management
Contribute to the development and evolution of science-driven publication strategies, including scientific communication platforms and data generation plans
Conduct comprehensive literature reviews and gap analyses to inform publication strategies and identify opportunities to address unmet scientific and educational needs
Actively participate in and help facilitate cross-functional Publication Team and Publication Review Team meetings, ensuring alignment and forward progress on key deliverables
Provide strategic and on-site support at key scientific meetings and congresses, including poster management, presentation reviews, and session coverage reporting
⁠Maintain familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing and publications
Contribute to the continuous improvement of publication-related policies, procedures, and operational processes to support organizational objectives and ensure compliance with internal and external regulatory expectations
Uphold Corcept’s Key Principles by driving collaboration, embracing possibilities, following the data, and leading by doing, ensuring all initiatives align with the Company’s ethics and patient-first principles