Protocol Writer I

Job not on LinkedIn

🕒 August 20

🇺🇸 United States – Remote

💵 $31 - $48 / hour

⏰ Full Time

🟢 Junior

🟡 Mid-level

✏️ Content Writer

👻 Ghost score 39%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Moffitt

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 1961

🏭 Manufacturing

🤝 B2B

🏗️ Construction

Manufacturing • B2B • Construction

Moffitt is an industrial ventilation company with more than 60 years of experience that designs, manufactures, and installs customized ventilation systems. It offers vents, fans, evaporative cooling, heating products and provides services including free on-site evaluations, ventilation design, advanced CFD and thermal modeling, manufacturing, installation, maintenance, and turn‑key project delivery for industrial customers. Moffitt serves facilities such as data centers, glass manufacturing, metals, paper & pulp/OSB, and power generation among others.

📋 Description

• Work with clinical investigators to write, edit, and complete clinical trial protocols and related documents • Edit, write, and gather technical and scientific documentation for clinical protocol proposals • Submit clinical trial projects accurately and on time to the Scientific Review Committee (SRC) • Work under the direction of the Principal Investigator (PI) • Ensure adherence to Moffitt's standards and regulatory requirements with the Clinical Trials Office • Work with external sponsors on study design • Support clinical science editing activities • Collaborate with Grant Administrators on clinical research portions of selected grant proposals • Develop protocols and related documents for NIH-defined clinical trials • Manage multiple concurrent projects and deadlines

🎯 Requirements

• Bachelor's Degree • Strong scientific/medical/health-related background with clinical research experience preferred • At least 2 years of relevant medical writing industry experience • Proven track record in writing high-quality regulatory documents • Preferred: MA, MS, MD, PharmD, or PhD with 1 year of scientific experience and/or clinical research experience • Ability to handle multiple concurrent projects with varying deadlines