Medical Writer - Perlmutter Cancer Center Clinical Trials Office
Listed on 2026-09-12
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Healthcare
Clinical Research, Medical Science
Medical Writer - Perlmutter Cancer Center Clinical Trials Office
Research -->
Administration
New York, NY
Full-Time/Regular
NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people. An integral part of NYU Langone Health, the Grossman School of Medicine at its core is committed to improving the human condition through medical education, scientific research, and direct patient care.
At NYU Langone Health, equity and inclusion are fundamental values. We strive to be a place where our exceptionally talented faculty, staff, and students of all identities can thrive. We embrace inclusion and individual skills, ideas, and knowledge. For more information, go to med.nyu.edu, and interact with us on Linked In, Glassdoor, Indeed, Facebook, X and Instagram.
We have an exciting opportunity to join our team as a Medical Writer - Perlmutter Cancer Center Clinical Trials Office.
The Medical Writer provides support for all Investigator Initiated Trials (IIT) at the Perlmutter Cancer Center (PCC) across all campuses and report into the Protocol Development Monitoring Unit (PDMU) at the Clinical Trials Office (CTO) with a reporting line to the PCC Molecular Oncology program. The Medical Writer also provides writing support for all posters, abstracts and publications related to Molecular Oncology IITs.
The Medical Writer may also provide additional monitoring support to verify data related to primary endpoints in IITs. The Medical Writer will provide IIT support will focus on Molecular Oncology. Serves as a liaison with the Investigator, Molecular Oncology Program, CTO, Biostatisticians and funding sponsor. In addition this position will provide resources to new investigators looking to develop an IIT as well as foster a program to support this.
- Demonstrates knowledge of the organizations Core Values and incorporates them into the performance of duties.
- Provides writing support for all IIT protocols with a focus in Molecular Oncology.
- Provides writing support for all posters, abstracts and publications.
- Works with the Quality Assurance Unit to verify data for endpoints related to analysis and/or publications.
- Develops a resource program/platform for investigators to present their ideas and receive support to initiate a Letter of Intent (LOI) with a funding sponsor.
Identifies mentorship opportunities for new investigators.
May also present at these programs/forums. - Serves as a liaison between Investigator, Molecular Oncology, funding sponsor, biostatistician and any other applicable parties involved in the development of an IIT.
- Provides support to the Program Manager for PDMU in reviewing of IITs.
- Participates in special projects and performs other duties as required.
- To qualify you must have a Bachelors degree preferably in science, public health, health education or a related field.
- 4 years of experience in clinical research or as a clinician.
- Effective oral, written, communication, interpersonal skills.
- Ability to identify, analyze and solve problems.
- Time management skills and ability to work well under pressure.
- Strong public speaking skills
- Excellent interpersonal, writing and verbal, presentation and communication skills.
- Ability to identify, analyze and solve problems
- Time management skills and ability to work well under pressure.
- Ability to multi-task while paying attention to detail.
- Proficiency in using various Microsoft Office applications such as Word, Excel, Access, Power Point and Outlook. Familiar with Internet applications
- Must be able to work and…
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