Clinical Scientist

SmartRecruiters, Inc.; Pearl River (NY); Presencial; USD 60.000 - 68.000; Jornada completa

Descripción de la vacante

SmartRecruiters, Inc. is seeking a Clinical Scientist to collaborate with the clinical lead and team to execute global clinical trial programs. The role focuses on planning, executing, and reporting activities across multiple studies.

The candidate will support protocol design, data review, safety oversight, and regulatory documentation, contributing to study integrity and timely publications. The position is based in the United States and offers a 12-month assignment with competitive hourly

Formación

• Collaborate on planning and execution of global clinical trials.
• Support study design, data review, safety oversight, and reporting.
• Prepare regulatory documents and publications.

Responsabilidades

• Assist in protocol and study design development.
• Review data and interpret results.
• Ensure scientific integrity and safety oversight.
• Prepare regulatory documents, study reports and publications.
• Coordinate with clinical lead and teams.

Conocimientos

Protocol and study design

Data review

Safety review

Regulatory documents

Educación

BA/BS Degree in science or health-related field

Descripción del empleo

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job.

Qualifications

The Clinical Scientist will work collaboratively with the clinical
lead and team to execute the clinical program(s). Their primary
deliverable is to assist in the assist in planning, executing and reporting of global clinical trials

The clinical
scientist support multiple tasks within the categories of 1) protocol and study design, strategy and training, 2) data review and interpretation, 3) study scientific integrity and oversight, 4) safety review and communication, 5) regulatory document, study report and publication preparation and review

Data review
Protocol Writing

BA/BS Degree in science or health-related field

3-5 years

Additional Information

$29/hr

12 months