Clinical Protocol Writer – Trials & Regulatory Docs

SPEROS; Northern (KY); Hybrid; USD 91,666,000 - 139,832,000; Full time

Job summary

Moffitt Cancer Center in Florida seeks a clinical research Protocol Writer to collaborate with clinical investigators to write, edit and complete clinical trial protocols and related documents for SRC submissions. Under the PI, you will gather technical and scientific materials to conceptualize and deliver proposals.

This role requires deadline-driven organization and ability to manage multiple projects, with 2+ years medical writing experience and a strong background in regulatory documents.

Qualifications

• Bachelor's Degree required.
• Experience in clinical research and medical writing preferred.
• Proven track record in writing high-quality regulatory documents.

Responsibilities

• Write, edit and complete clinical trial protocols and related documents for SRC submissions.
• Collaborate with Clinical Trials Office and PI on study design and documentation.
• Coordinate with external sponsors on protocol development and NIH-defined trials.

Skills

Clinical research writing

Regulatory documentation

Medical writing

Deadline management

Education

Bachelor's Degree

MA/MS/MD/PharmD/PhD with science/clinical experience

Job description

Moffitt Cancer Center in Florida seeks a clinical research Protocol Writer to collaborate with clinical investigators to write, edit and complete clinical trial protocols and related documents for SRC submissions. Under the PI, you will gather technical and scientific materials to conceptualize and deliver proposals.

This role requires deadline-driven organization and ability to manage multiple projects, with 2+ years medical writing experience and a strong background in regulatory documents.