Senior Medical Writer

Joulé; Village of Tarrytown (NY); Hybrid; USD 125,000 - 150,000; Full time

Job summary

A leading company seeks a Senior Medical Writer for a 6-month contract in Armonk, NY. The role involves writing clinical documents, managing projects, and collaborating with teams. Ideal candidates should have strong clinical research knowledge and experience in medical writing. This hybrid position offers a competitive hourly pay range of $65-75.

Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Plan

Qualifications

• Minimum of 3 years relevant Medical Writing experience.
• Working knowledge of biostatistics.

Responsibilities

• Write clinical documents including CSRs, protocols, ICFs, and narratives.
• Drive document development meetings and manage processes.

Skills

Organizational Skills

Interpersonal Skills

Communication Skills

Knowledge of Clinical Research

Education

Bachelor's Degree

Advanced Degree

Tools

MS WORD

Adobe Acrobat

PowerPoint

Electronic Document Management Systems

Job description

1 day ago Be among the first 25 applicants

Title: Senior Medical Writer

Location: Armonk, NY (hybrid)

Duration: 6 month contract, possible to renew

Pay range: $65-75/HR

Start Date: ASAP

Title: Senior Medical Writer

Location: Armonk, NY (hybrid)

Duration: 6 month contract, possible to renew

Pay range: $65-75/HR

Start Date: ASAP



The Senior Medical Writer (SMW) works with team members and independently to write the content of clinical documents that may include CSRs, protocols, ICFs, narratives and IBs in a variety of therapeutic areas. Opportunities to contribute to other regulatory documents may be provided. The SMW tracks his/her own writing projects and is responsible for adhering to regulatory guidelines and department document standards. The SMW may also serve as lead for a compound and may also review the work of junior/outsourced writers as well as review CSR-related documents (Statistical Analysis Plans, TFLs) to help ensure appropriate content for inclusion.

In this role, a typical day might include the following:

• Works with the clinical team, to write the content of clinical documents that may include CSRs, protocols, ICFs, narratives and IBs in a variety of therapeutic areas. Opportunities to write or contribute to other Regulatory documents may be provided


• Represents MW at meeting and drives document development meetings


• Participates in process improvement initiatives, working groups, etc. within MW and throughout Global Development


• Manages processes and organizes priorities; solves problems; fosters collaboration to resolves conflict


• May review the work of junior and outsourced MWs


• May review CSR-related documents (Statistical Analysis Plans, TFLs) to help ensure appropriate content for inclusion


• Writes in plain language style as appropriate (eg, for ICF), explains complex medical/scientific concepts (such as medical procedures, clinical study design, and drug mechanisms) to a lay or patient audience

This job might be for you if you have:

• Strong knowledge of the clinical research process and regulations/guidelines


• Clinical document reading, writing, and editing experience


• Strong organizational, interpersonal and communication skills


• Strong knowledge of MS WORD, Adobe Acrobat, PowerPoint, and electronic document management systems


• Ability to manage multiple projects


• Familiarity with ICH GCP guidelines

To be considered for this role, you must have

• Bachelor's degree (advanced degree preferred) and minimum of 3 years of relevant MW experience including working knowledge of biostatistics.

System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.



System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.



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Ref: #568-Clinical

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Marketing, Public Relations, and Writing/Editing

• Industries

  Staffing and Recruiting

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