Job Description

A major medical leader in healthcare practice management solutions has a need for a Medical Writer . This is a hybrid, full-time position located in Jamaica, NY.

This position is an integral and necessary piece of the plan to achieve these goals. The medical writer will not only be experienced in research grant writing but will also have the ability to help publish research papers and teach/mentor medical students and residents.

Responsibilities:

• Independently interpret complex data and develop high-quality strategic scientific documents including abstracts and full-length manuscripts.
• Coordinate the review, approval, submission and production of publications.
• Participate in the planning, development, and implementation of the medical educational plan, publication plan, and other scientific programs.
• Collaborate with investigators and biostatisticians to ensure deliverables are completed per time and quality goals.
• Develop documents for assigned programs in compliance with standard operating procedures
• Work with cross functional internal teams to ensure wide acceptability of documents and consensus of content.
• Support key strategic meetings with internal and external stakeholders and manage the output from these meetings. Oversee oustsourced medical writings projects and the associated vendor(s), as applicable.
• Critically analyze, synthesize and present complex information.

Education & Work Experience:

• An advanced degree in life science is preferred (e.g., masters's degree or equivalent).
• Medical education or relevant experience in ta related field.
• Proven content development management experience.
• Excellent oral and written communications skills.
• Excellent analytical skills.
• Excellent organizational skills and attention to detail, with absolute commitment to quality.
• Ability to think creatively and identify and work to develop unique sevice offerings.
• Ability to work independently in a face paced environment; self-motivated.
• Ability to participate and interact effectively with the team.
• Ability to manage time, multi-task, and handle a high volume of work in a fast-paced environment.
• Advanced proficiency in Microsoft Office Suite (e.g. Word, Excel, Power Point and Outlook.)
• Ability to teach and mentor others about medical writing.

Skills & Knowledge

• Ability to interpret, evaluate and communicate (in a variety of formats and styles) complex scientific and clinical data.
• Expertise in use of online and other data sources for literature searches and information.
• General Knowledge of the drug development and approval processes.
• Ability to work collaboratively and coordinate the efforts of team members to resolve comments and complete deliverables.
• Ability to manage/prioritize multiple projects under general supervision, working in a fast-paced environment.
• Flexible and able to adapt to changing deadlines and priorities.
• Excellent written, verbal and interpersonal communications skills.
• Highly attentive to detail.
• Self-motivated and able to self-manage effort to maintain alignment with strategy and corporate goals.

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

PRO038

Job Tags

Full time, Work experience placement, Local area, Flexible hours,

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