Director, Global Scientific Publications (East Coast Based Candidates …
Axsome Therapeutics IncSalary not specified
Full Time
Expert & Leadership (9+ years)
Not SpecifiedCompensation
Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceutical, Biotech, Medical Device, Medical CommunicationsIndustries
Requirements
Candidates must possess an advanced degree in science such as a PhD, PharmD, or MD, with CMPP preferred. A minimum of 2 years of relevant experience in medical publications, including manuscripts, posters, abstracts, podium presentations, scientific platforms, and publication extenders, is required. Demonstrated organizational, analytical, and interpersonal communication skills are necessary, along with the ability to analyze and interpret scientific data, multitask, work independently, and manage projects within tight deadlines with limited direction. Experience with established professional medical editorial processes, such as AMA style, and working knowledge of ethical guidelines like ICMJE and GPP2022 are also mandatory. Experience in Pulmonary, Dermatology, and/or Neuroscience is considered a plus.
Responsibilities
The Senior Associate Scientific Director will be responsible for developing high-quality, medically accurate content for assigned projects under the supervision of a Senior Scientific Director. This includes creating scientific content to support brand goals, engaging with Key Opinion Leaders (KOLs) and Healthcare Professionals (HCPs), managing project resources and timelines, and partnering with client services to ensure projects are delivered on time and within budget. Additional tasks involve conducting background research, data-checking, and reference annotation.
Skills
Medical Communications
Manuscript Development
Poster Development
Abstract Development
Podium Presentations
Scientific Platforms
Publication Extenders
KOL Engagement
HCP Engagement
Project Management
Timeline Management
Budget Management
Scientific Research
Data Checking
Reference Annotation
CMPP
The Lockwood Group, LLC
Healthcare consulting for drug development support
About The Lockwood Group, LLC
The Lockwood Group provides consulting services specifically for the healthcare and pharmaceutical industries, focusing on clients in the later stages of drug development, particularly after Phase 2 clinical trials. The company assists pharmaceutical and biotech firms by creating strategic publication plans that communicate scientific data and research findings accurately and in compliance with regulatory standards. They also support clients during the prelaunch phase of their products by identifying market needs and collaborating through the launch process to ensure success. A unique aspect of The Lockwood Group is its medical animation affiliate, Random42, which produces engaging and scientifically accurate visual content to help convey complex information. Their business model is based on service fees for consulting and project work, with a commitment to delivering high-quality communications and strategic support to help clients thrive in the competitive healthcare landscape.
Stamford, ConnecticutHeadquarters
2007Year Founded
ACQUISITIONCompany Stage
Consulting, HealthcareIndustries
201-500Employees