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Writing Associate Jobs in New York (NOW HIRING)

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Shipping/Receiving Manager

South Hackensack, NJ · On-site

Exceptional English communication skills, both oral and written * Associates degree and higher preferred * Successful completion of drug test, and general background check Additional Information All ...

ACORD Corporation

Content Associate

Little Falls, NJ

The Content Associate will assist with writing, copy editing, research, social media, and overall corporate communications. The Content Associate will work primarily in the Communications department ...

ACORD Corporation

Content Associate

Little Falls, NJ

The Content Associate will assist with writing, copy editing, research, social media, and overall corporate communications. The Content Associate will work primarily in the Communications department ...

ACORD Corporation

Content Associate

Little Falls, NJ · On-site

The Content Associate will assist with writing, copy editing, research, social media, and overall corporate communications. The Content Associate will work primarily in the Communications department ...

Grant Associates Inc.

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Bilingual Intake Associate

Brooklyn, NY · On-site

$22/hr

Bilingual Intake Associate (Sunset Park, Brooklyn, NY) Starting Pay: $22.00/hr. Description The ... written and verbal communication skills. · Bilingual (English and Spanish) required. · Experience ...

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Writing Associate information

What is a writing associate?

Writing Associates are professionals who assist students, faculty, or professionals with writing projects. They provide feedback, guidance, and support to help individuals improve the clarity, structure, and effectiveness of their written work. Writing Associates often work in academic settings, such as writing centers or universities, but can also be found in corporate or nonprofit environments. Their goal is to empower writers to develop their skills and produce high-quality documents.

How does a writing associate typically collaborate with other team members during the content development process?

A Writing Associate often works closely with editors, subject matter experts, and designers to ensure content accuracy, clarity, and alignment with project goals. Collaboration may involve participating in brainstorming sessions, revising drafts based on feedback, and adapting writing styles to suit various platforms. Regular communication and feedback loops are essential, as Writing Associates need to balance creative input with organizational guidelines and deadlines. This teamwork not only enhances content quality but also provides opportunities to learn from experienced colleagues.

What are the key skills and qualifications needed to thrive as a writing associate, and why are they important?

To thrive as a Writing Associate, you need strong writing, editing, and research skills, typically supported by a bachelor's degree in English, communications, or a related field. Familiarity with style guides (such as APA or MLA), word processing software, and collaborative platforms like Google Docs is often required. Exceptional communication, critical thinking, and adaptability help you tailor content and feedback to diverse audiences. These competencies are crucial for producing clear, effective writing and supporting the development of others’ written work.

What is the difference between Writing Associate vs Writing Tutor?

AspectWriting AssociateWriting Tutor
CredentialsTypically requires a bachelor's degree, strong writing skillsUsually undergraduate or graduate students with good writing abilities
Work EnvironmentOften works in academic or professional settings, supporting writing projectsPrimarily works in tutoring centers or academic support services
Employer & IndustryUniversities, colleges, or writing centersEducational institutions, tutoring centers

While both roles involve supporting writing, a Writing Associate often collaborates on projects and may have more responsibilities related to content development, whereas a Writing Tutor primarily provides one-on-one assistance to students to improve their writing skills.

What are the most commonly searched types of Writing jobs in New York?

The most popular types of Writing jobs in New York are:

What are popular job titles related to Writing Associate jobs in New York?

For Writing Associate jobs in New York, the most frequently searched job titles are:

What job categories do people searching Writing Associate jobs in New York look for?

The top searched job categories for Writing Associate jobs in New York are:

What cities in New York are hiring for Writing Associate jobs?

Cities in New York with the most Writing Associate job openings:

Writing Associate jobs near you

Sr. Manager, Medical Writing

Medical Affairs

Somerset, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 23 days ago

Job description

Terumo Medical Corporation (TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high-quality medical devices used in a broad range of applications for numerous areas of the healthcare industry. TMC places a premium on providing customers with world-class products, training and education programs that drive clear economic value, better clinical outcomes and improved quality of life for patients. TMC is part of Tokyo-based Terumo Corporation; one of the world’s leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide and operations in more than 160 nations. Terumo Medical Corporation is comprised of two strategic business divisions: Terumo Interventional Systems and Terumo Medical Products.

We believe that the future is bright for everyone at Terumo. We work with the future in mind to generate lasting change, create a bigger impact and produce greater outcomes for today, and for decades to come.

At Terumo we believe in the power of personal growth and will encourage you to get in the driver's seat - progressing in the direction you want to go by deepening your skills throughout your career. We want you to be bold, think outside the box, experiment, innovate and deliver what's next for quality healthcare. You will be part of a collaborative, respectful and resilient team of associates and leaders around the world, working together as partners to achieve more than you thought possible, providing real-world, impactful solutions for patients.

Join us and help shape wherever we go next!

Advancing healthcare with heart

Job Summary

Sr. Manager Medical Writing, manages and oversees the work of medical writing teams to support clinical and regulatory submissions (e.g., clinical evaluation reports, clinical study reports,) and product development. This role partners with Engineering and R&D, Clinical Affairs, Professional & Clinical Education, Regulatory Affairs, Quality Systems, Marketing, Sales as well as external stakeholders, to include FDA, NB, PMDA, KOL, HCP, IRB and publishers. The role reports directly to the Senior Medical Director, Scientific Data & Communications.

Job Details/Responsibilities
  • Lead, mentor, and develop a team of medical writers responsible for clinical evaluation, scientific communication, and regulatory documentation. Oversee workload allocation, project prioritization, and timely delivery of high‑quality documents; and lead  talent development in alignment with growth strategies of the department. 40% of role.
  • Provide technical guidance, writing expertise, and scientific oversight to ensure consistency, accuracy, and compliance with applicable regulations and internal standards. Develop and maintain SOPs, work instructions, and best practices related to medical writing. Serve as subject‑matter expert in medical writing standards, expectations of regulatory bodies, and scientific communication. 20% of role. 
  • Review and approve the team outputs including regulatory documents / scientific communication / clinical research related documents. 20% of role. 
  • Assure Quality Oversight & Regulatory Compliance. Oversee literature review methodologies, literature database management practices, and interpretation of scientific evidence. 10% of role.
  • Build and manage internal partnerships with PACE, Clinical Operations, Regulatory Affairs, Quality System and Marketing R&D and Engineering. 10% of role. 
Working Conditions/Physical Requirements
  • This position requires up to 10% of travel
  • Manage a team of 3 direct reports 
Knowledge, Skills and Abilities (KSA)
  • Strong leadership in project and team management, including coaching and performance oversight.
  • Excellent organizational and time management skills
  • Expertise in medical writing processes, regulatory requirements (FDA, EU MDR), with GCP, and ICH guidelines
  • Ability to adapt to changing priorities
  • Knowledge of biomedical statistics, clinical literature review
  • Highly proficient in using Microsoft Office applications (Word, Excel, PowerPoint) and EndNote
  • Expertise in conducting focused literature searches on PubMed, Embase, MedLine or other similar medical literature databases
  • Knowledge and understanding of PICO methodology
  • Ability to function in a self-directed manner with a high degree of independence
  • Strong verbal, written, and interpersonal communication skills
  • Ability to persuasively influence external medical professionals
  • Effective analytical and problem-solving skills
  • Excellent interpersonal and effective leadership, verbal and written communication skills and effectively work across departments with diverse needs
Qualifications/ Background Experiences
  • Advance Degree ((Ph.D., MD, Sc.D, MA/MS or MPH) in a medical/biomedical/scientific discipline with a minimum of 5 years of experience in medical writing of regulatory documentation (clinical research documentation is optional) OR Bachelor’s Degree, preferably in life sciences with 10 years  of relevant work experience; OR equivalent combination of education, training and relevant experience.
  • Demonstrated relevant track record in people management how many years?
  • Experience in medical or scientific writing and creating content for scientific presentations
  • Demonstrated experience in the development of regulatory/clinical submissions, preferably as a medical writer for pharmaceutical, CRO, or medical device clients, a strong plus.
  • Experience with Class III devices and CER development under MDR preferred

It is Terumo’s policy to provide equal employment opportunity to all its employees and applicants for employment regardless of their race, creed, color, national origin, age, ancestry, nationality, marital or domestic partnership or civil union status, sex, pregnancy, gender identity or expression, disability status, liability for military service, protected veteran status, sexual orientation, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing), or any other category protected by law. As a Company, we value diversity of background and opinion, and prohibit discrimination or harassment on the basis of any legally protected class in the areas of hiring, recruitment, promotion, transfer, demotion, training, compensation, pay, fringe benefits, layoff, termination or any other terms and conditions of employment.

Final compensation packages may be higher or lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. We provide competitive and comprehensive benefit options which include: annual bonus, paid vacation, paid holidays, health, dental and vision benefits, 401(k), with matching contributions, tax advantage savings accounts, legal plan, voluntary life and AD&D insurance, voluntary long-term disability, short term disability, critical illness and accident insurance, parental leave, personal leave, tuition reimbursement, travel assistance, and an employee assistance program. The salary range for this role is $150,000 - $198,000 based on experience plus a 20% target bonus. 

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