Joulé
Associate Director, Medical Writing
Joulé, Raritan, New Jersey, us, 08869
Title: Manager, Associate Director, Medical Writing
Check all associated application documentation thoroughly before clicking on the apply button at the bottom of this description.Location: RemoteSalary: 150-165K depending on experienceType: EmbeddedStart Date: ASAP
Leading Pharmaceutical Company located in NJ is hiring a Associate Director, Medical Writing w/ 5+ years industry experience. If you want to be a part of this groundbreaking work, please apply!
Job Description:Essential Functions:
Provide expert writing and editing support to ensure timely production of high-quality documents (abstracts, posters, slide presentations, manuscripts, letters to editor, etc.) for publication in medical/scientific journals or presentation at meetings. (50%)
Manage and/or review and interpret data and source documents for information required for publication.
Assist in table and figure mock-up development.
Actively engage internal and external authors and other key stakeholders in the development of publication plans and strategy at the individual dataset, study, and/or compound level.
Skillfully manage projects through publication review system (JPUBS)
Provide direction, oversight and editing for outsourced medical writers and project management of selected therapeutic area publications. (50%)
Qualifications:
A PhD, MD, or PharmD with a minimum of 5 years of relevant pharmaceutical/scientific experience is required OR a Master’s (or other advanced degree) with a minimum of 8 years relevant pharmaceutical/scientific experience is required
Research experience (including compilation of research reports or publications) in academia or the pharmaceutical industry or as part of a PHD, Pharm.D or postdoctoral program is preferred
Demonstrated ability to interpret and organize clinical and scientific data is required
Experience with MS Office Suite (Excel, Word, PowerPoint) is required
The ability to work well independently as well as part of a team is required
Project management experience is preferred
The ability to stay organized, manage time, and work on multiple documents/projects at once is required
Knowledge in across several therapeutic areas including immunology, neuroscience and/or oncology is preferred
Benefits:System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.
Check all associated application documentation thoroughly before clicking on the apply button at the bottom of this description.Location: RemoteSalary: 150-165K depending on experienceType: EmbeddedStart Date: ASAP
Leading Pharmaceutical Company located in NJ is hiring a Associate Director, Medical Writing w/ 5+ years industry experience. If you want to be a part of this groundbreaking work, please apply!
Job Description:Essential Functions:
Provide expert writing and editing support to ensure timely production of high-quality documents (abstracts, posters, slide presentations, manuscripts, letters to editor, etc.) for publication in medical/scientific journals or presentation at meetings. (50%)
Manage and/or review and interpret data and source documents for information required for publication.
Assist in table and figure mock-up development.
Actively engage internal and external authors and other key stakeholders in the development of publication plans and strategy at the individual dataset, study, and/or compound level.
Skillfully manage projects through publication review system (JPUBS)
Provide direction, oversight and editing for outsourced medical writers and project management of selected therapeutic area publications. (50%)
Qualifications:
A PhD, MD, or PharmD with a minimum of 5 years of relevant pharmaceutical/scientific experience is required OR a Master’s (or other advanced degree) with a minimum of 8 years relevant pharmaceutical/scientific experience is required
Research experience (including compilation of research reports or publications) in academia or the pharmaceutical industry or as part of a PHD, Pharm.D or postdoctoral program is preferred
Demonstrated ability to interpret and organize clinical and scientific data is required
Experience with MS Office Suite (Excel, Word, PowerPoint) is required
The ability to work well independently as well as part of a team is required
Project management experience is preferred
The ability to stay organized, manage time, and work on multiple documents/projects at once is required
Knowledge in across several therapeutic areas including immunology, neuroscience and/or oncology is preferred
Benefits:System One offers eligible employees health and welfare benefits coverage options, including medical, dental, vision, spending accounts, life insurance, voluntary plans, and participation in a 401(k) plan.