Clinical Research Data Analyst II – Endocrine Surgery

Medical University of South Carolina; Charleston (SC); On-site; USD 26,000 - 44,000; Full time

Job summary

Medical University of South Carolina (MUSC) in Charleston, SC seeks a Statistical and Research Analyst II to manage data in endocrine surgery databases, assist in drafting clinical research protocols, and support data analysis and manuscript preparation.

The role requires independent work, with responsibilities spanning data entry, protocol submissions to PRC/IRB, and updating research databases, along with potential grant writing support.

Qualifications

• Bachelor's degree in biostatistics, epidemiology, public health, or clinical research preferred. A master's degree would be helpful.
• Proficiency with Word, Excel, PowerPoint, and statistical software (SAS, SPSS, etc).
• Two years work experience as Statistical and Research Analyst I; a bachelor’s degree with mathematics/statistics may substitute for the required experience.

Responsibilities

• Collect/enter data into Endocrine Surgery clinical databases (35%).
• Assist with clinical studies, including testing new systems to be used intraoperatively (20%).
• Assist in drafting/submission/maintenance of clinical research protocols (PRC/IRB, progress reports, renewals) (20%).
• Update and maintain IRB protocols and research databases (10%).
• Assist with data analysis for clinical projects (5%).
• Assist with drafting/writing/submission of abstracts/manuscripts/grants (5%).
• Other duties as assigned (5%).

Skills

Data entry

Data analysis

Clinical research

IRB/protocol prep

Statistical software

Education

Bachelor's degree in biostatistics/epidemiology/public health/clinical research

Tools

Word

Excel

PowerPoint

SAS

SPSS

SATA

Job description

Medical University of South Carolina (MUSC) in Charleston, SC seeks a Statistical and Research Analyst II to manage data in endocrine surgery databases, assist in drafting clinical research protocols, and support data analysis and manuscript preparation.

The role requires independent work, with responsibilities spanning data entry, protocol submissions to PRC/IRB, and updating research databases, along with potential grant writing support.