PROTOCOL WRITER I|无
PROTOCOL WRITER I
作为佛罗里达州唯一的国家癌症研究所所指定的综合癌症中心，莫菲特雇佣了来自世界各地的一些最好的和最聪明的人才。加入一个致力于塑造我们想象的未来的近11000名团队。莫菲特被公认为全国最佳和最聪亮的公司之一，并一直被评为坦帕湾时报头的工作场所之一。摘要：临床研究协议作者与临床研究人员合作，以准确及及时向科学审查委员会提交临床试验项目所需的临床试题议定书和相关文件。主任调查员 (PI) 的指导下，编辑，撰写并收集构想，准备和交付 SRC 的完整临床协议建议所需的技术和科学文档。临床研究协议作者与临床调查人员合作，以准确及及时向科学审查委员会提交临床试验项目所需的临床试题议定书和相关文件。主任调查员 (PI) 的指导下，他编辑，撰写并收集构想，准备和交付完整的临床协议建议所需的技术和科学文档。职责还包括与临床试验办公室合作，确保遵守莫菲特的标准和监管要求以及与 PI 一起，在研究设计上与外部赞助商合作。次级责任包括支持临床科学编辑活动。对于包括临床试题的选择补贴，该职位将与赠款管理员合作，以制定建议的临床研究部分，包括根据 NIH 定义的临床试点所需的 PHS 人类主体和临床试卷信息表格中概述的协议和相关文件。职位需要基于最后期限的方法和处理多个同时项目的能力，每个项目都有不同的执行截止日期。最低要求：学士学位 有强大的科学/医学/健康相关背景，具有临床研究
查看英文原文
Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.
As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.
Summary
With an emphasis on investigator-initiated, early phase clinical trials, the clinical research Protocol Writer works with clinical investigators to write, edit and complete clinical trial protocols and related documents necessary to accurately and timely submit clinical trial projects to the Scientific Review Committee (SRC). Works under the direction of the Principal Investigator (PI) to edit, write, and gather technical and scientific documentation required to conceptualize, prepare, and deliver complete clinical protocol proposals to the SRC.Protocol Writer I
With an emphasis on investigator-initiated, early phase clinical trials, the clinical research Protocol Writer works with clinical investigators to write, edit and complete clinical trial protocols and related documents necessary to accurately and timely submit clinical trial projects to the Scientific Review Committee (SRC).
Works under the direction of the Principal Investigator (PI) to edit, write, and gather technical and scientific documentation required to conceptualize, prepare, and deliver complete clinical protocol proposals to the SRC.
Responsibilities also include working with the Clinical Trials Office to ensure adherence to Moffitt's standards and regulatory requirements and with the PI, working with external sponsors on study design.
Secondary responsibilities include supporting clinical science editing activities. For select grants that include clinical trials, the position will work with Grant Administrators on the clinical research portion of the proposal, including developing the protocol and related documents outlined in the PHS Human Subjects and Clinical Trials Information Form as required for NIH defined clinical trials.
Position requires deadline-driven approach and ability to handle multiple concurrent projects, each with varying deadlines for execution.
Minimum Requirements:
Bachelor's Degree
Strong scientific/medical/health-related background with clinical research experience preferred.
Experience must include at least 2 years of relevant medical writing industry experience and a proven track record in writing high-quality regulatory documents.
Preferred Qualifications:
MA, MS, MD, PharmD, or PhD with 1 year of scientific experience and/or clinical research experience.
Salary Range
$31.99 - $48.80Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.
We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.
Moffitt Career Site
If you have the vision, passion, and dedication to contribute to our mission,
then we have a place for you!
1. Equal Employment Opportunity
Moffitt Cancer Center is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.
2. Reasonable Accommodation
Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Moffitt endeavors to make moffitt.org/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact one of the Human Resources receptionists by phone at 813-745-7899 or by email at . This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.
Read more information about your EEO rights under the law.
Transparency in Coverage Rule
Originally posted on Himalayas