Associate Director, Global Medical Affairs Publication Operations

About the role

We are searching for the best talent for an Associate Director, Global Medical Affairs Publication Operations located in Raritan, NJ.

Responsibilities

• Scientific publication writing including abstracts, posters/oral presentations, and manuscripts, etc.
• Overall production of publications and compliance with standard operating procedures/industry standards.
• Partners with product team personnel to advance publication-related goals of the team.
• Manage and/or review and interpret data and source documents for information required for publication.
• Engage internal and external authors and other key stakeholders in the development of publication plans and strategy.
• Provide direction, oversight and editing for contract medical writers and junior-level medical writers.
• Develop or update publication-related SOPs and Guidelines.
• Participate in the development and maintenance of document templates, style guides, electronic document management and publication review and approval system.
• Partners with relevant stakeholders to efficiently deliver assigned encores.

Requirements

• A PhD, PharmD, MD or equivalent degree with a minimum of 8 years of relevant pharmaceutical/scientific experience is required OR a Master’s (or other advanced degree) with a minimum of 10 years relevant pharmaceutical/scientific experience is required.
• Research experience (including compilation of research reports or publications) in academia, the pharmaceutical industry, medical communication agency or as part of a PhD, PharmD or postdoctoral program is preferred.
• Demonstrated ability to interpret and organize scientific data is required.
• The ability to work well independently and as part of a team is required.
• Project management experience is preferred.
• Knowledge across several therapeutic areas such as oncology, neuroscience, and immunology is preferred.
• Experience with medical writing document standards and processes is preferred.
• Experience using workflow management tool (e.g., JPUBS, Datavision, or PubSTRAT) is preferred.
• CMPP certification is preferred.
• Up to 10% travel.

Qualifications

PhD, PharmD, MD or equivalent degree with a minimum of 8 years of relevant pharmaceutical/scientific experience is required OR a Master’s (or other advanced degree) with a minimum of 10 years relevant pharmaceutical/scientific experience is required.

Research experience (including compilation of research reports or publications) in academia, the pharmaceutical industry, medical communication agency or as part of a PhD, PharmD or postdoctoral program is preferred.

Demonstrated ability to interpret and organize scientific data is required.

The ability to work well independently and as part of a team is required.

Project management experience is preferred.

Knowledge across several therapeutic areas such as oncology, neuroscience, and immunology is preferred.

Experience with medical writing document standards and processes is preferred.

Experience using workflow management tool (e.g., JPUBS, Datavision, or PubSTRAT) is preferred.

CMPP certification is preferred.

Up to 10% travel.

Skills

• Knowledge across several therapeutic areas such as oncology, neuroscience, and immunology.
• Experience with medical writing document standards and processes.
• Experience using workflow management tool (e.g., JPUBS, Datavision, or PubSTRAT).
• CMPP certification.

Benefits

Additional information can be found through the link below.

https://www.careers.jnj.com/employee-benefits