Clinical Data Reporting Specialist

Tubman Technologies Inc.; Alpharetta (GA); On-site; USD 70,000 - 90,000; Full time

Job summary

A pharmaceutical research firm is seeking a Clinical Data Reporting Specialist in Alpharetta, GA. This role involves supporting clinical research through data analysis and reporting using SAS software. The ideal candidate will possess a Bachelor’s degree in Clinical Informatics or a related field, with strong knowledge of clinical data management and statistical methodologies. Excellent communication and collaboration skills are essential to work with cross-functional teams, while ensuring compliance with FDA guidelines. Relocation may be required several times a year.

Qualifications

• Education in Clinical Informatics, Health Informatics or related field.
• Proficiency in SAS for clinical data manipulation and statistical analysis.
• Excellent communication and time management skills.

Responsibilities

• Support research and development through clinical data analysis.
• Perform ETL processes using SAS or equivalent software.
• Generate reports for clinical trials and regulatory submissions.

Skills

Proficiency in SAS or equivalent software

Knowledge of clinical data management principles

Understanding of statistical methodologies

Familiarity with regulatory guidelines

Ability to present complex clinical data

Use of BI tools for data visualization

Excellent communication skills

Organizational skills to meet deadlines

Education

Bachelor’s degree or foreign equivalent in Clinical Informatics

Tools

SAS

Tableau

Power BI

Job description

Current multiple job opportunities needed for immediate FT employment.

TITLE: Clinical Data Reporting Specialist

JOB DESCRIPTION

The Clinical Data Reporting Specialist will be responsible for supporting pharmaceutical research and development through clinical data analysis, reporting, and business intelligence solutions. The specialist will utilize SAS (or equivalent) software for data extraction, transformation, and loading (ETL), conduct statistical analyses, and generate regulatory-compliant reports. The role requires collaboration with cross-functional teams to ensure data integrity, compliance with industry standards, and timely delivery of clinical insights.

JOB DUTIES

Perform data extraction, transformation, and loading (ETL) processes using SAS (or equivalent) software.

Develop and execute SAS (or equivalent) programs for statistical analysis and clinical data reporting.

• Generate standard and ad-hoc reports to support clinical trials and regulatory submissions.
• Collaborate with cross-functional teams to interpret data and provide analytical insights.
• Utilize Business Intelligence (BI) tools to visualize and communicate clinical data trends.
• Ensure compliance with applicable regulatory guidelines, including FDA requirements.
• Contribute to improving data management practices and standard operating procedures (SOPs).

RELOCATION

Relocation to various unanticipated client sites across USA required up to 4 times per year.

MINIMUM REQUIREMENTS

Education: Bachelor’s degree or foreign equivalent in Clinical Informatics, Health Informatics, Pharmaceutical Sciences, Clinical Analytics, or a related field.

Knowledge, Skills, and Abilities (KSAs): Must have knowledge, skills, and abilities in the following (can be gained through education, training, or experience):

• Proficiency in SAS (or equivalent) software for clinical data manipulation, statistical analysis, and reporting.
• Knowledge of clinical data management principles and pharmaceutical industry standards.
• Understanding of statistical methodologies and clinical trial processes.
• Familiarity with regulatory guidelines (e.g., FDA) for clinical data reporting and compliance.
• Ability to interpret and present complex clinical data effectively.
• Use of Business Intelligence (BI) tools (e.g., Tableau, Power BI) for data visualization.
• Excellent communication and collaboration skills in cross-functional environments.
• Organizational and time management skills to meet regulatory deadlines.
• Ability to follow standard operating procedures and regulatory protocols.

Minimum Requirements Apply To The Positions Listed Above.

Please Refer To This Advertisement. No Phone Calls Please. Equal Opportunity Employer.

Please Mail Your Resume To:

HR Manager

Tubman Technologies, Inc.

13010 Morris Road, Suite 600

Alpharetta, GA 30004