Senior Clinical Trials Data & Reporting Specialist

BioSpace; North Chicago (IL); On-site; USD 110,000 - 170,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Job summary

AbbVie is seeking a dedicated professional to build data and information for internal clinical trial documents and reports. You will support multi-tasking across several reports and ensure scientific integrity throughout.

You will prepare reports, assist with Phase 1 planning, review protocols, and analyze data to support ongoing safety and efficacy reviews while maintaining high-quality deliverables.

Qualifications

• Bachelor's/Master's degree in Science with 7+ years in pharmaceutical industry.
• Understanding of clinical study principles.
• Must possess good oral and written communication skills.
• Proficient in using computer to analyze clinical study data and create presentations.
• Knowledge of complex scientific analyses, business procedures, and project leadership.
• Experience supporting clinical research, drug development and/or therapeutic area operations.
• Proven record of successful projects.
• Ability to produce high-quality work with attention to detail.

Responsibilities

• Prepare scientific reports and presentations related to clinical trials using available software and templates.
• Assists in constructing phase 1 clinical study planning documents and writes Phase 1 protocols.
• Review clinical protocols and key decisions impacting project timelines with management.
• Ensure compliance with procedures and directives issued by management.
• Analyze clinical study data using software to support blinded efficacy and safety reviews.
• Receive and complete tasks from Therapeutic Area MD or Scientific Staff within timelines.
• Maintain scientific integrity of processes by applying electronic document conventions.
• Integrate trial data across studies and communicate issues to peers and management.
• Perform literature/competitive intelligence searches to resolve scientific problems.
• Participate in process improvement initiatives and management reviews.
• Mentor therapeutic area personnel and maximize productivity.

Skills

Clinical study principles

Oral and written communication

Data analysis

Reports and presentations

Project leadership

Clinical research experience

Statistical data analysis

Independent work

Education

Bachelor's/Master's degree in Science (7+ years in pharma)

Tools

Statistical software

MS Office (Word/PowerPoint)

Reporting templates/software

Job description

AbbVie is seeking a dedicated professional to build data and information for internal clinical trial documents and reports. You will support multi-tasking across several reports and ensure scientific integrity throughout.

You will prepare reports, assist with Phase 1 planning, review protocols, and analyze data to support ongoing safety and efficacy reviews while maintaining high-quality deliverables.