Clinical Trials Reporting & Data Specialist

Allergan

Chicago, Northern (IL, KY)

Hybrid

USD 110,000 - 160,000

Full time

3 days ago
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Job summary

AbbVie in Chicago is seeking a senior scientific reporting specialist to prepare internal clinical trial documents and reports. You will manage multiple reports across studies, ensuring scientific integrity and timely delivery.

The role requires strong communication, data analysis skills, and experience with clinical research and drug development. Excellent collaboration and leadership abilities are essential for success in this fast-paced environment.

Qualifications

  • Understanding of clinical study principles.
  • Must possess good oral and written communication skills.
  • Proficient in using computer to analyze clinical study data, generate reports and create presentations, posters and manuscripts.
  • Knowledge of complex scientific analyses and project leadership.
  • Experience supporting clinical research, drug development and/or therapeutic area operations.
  • Proven record of successful projects.

Responsibilities

  • Prepare scientific reports and presentations related to clinical trials using available software and templates.
  • Assist in constructing phase 1 clinical study planning documents and write Phase 1 protocols.
  • Review clinical protocols and key decisions impacting project timelines with management.
  • Comply with procedures in IQS documents and study protocols and directives from 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 timeline.
  • Ensure scientific integrity of all processes by electronic document conventions and processes.
  • Integrate clinical trial data across studies and identify issues for management.
  • Perform literature/competitive intelligence searches to resolve problems.
  • Participate on teams for process improvement initiatives and monitor timelines.

Skills

Communication skills
Clinical study principles
Data analysis
Project leadership

Education

Bachelor's/Master’s in Science

Job description

AbbVie in Chicago is seeking a senior scientific reporting specialist to prepare internal clinical trial documents and reports. You will manage multiple reports across studies, ensuring scientific integrity and timely delivery.

The role requires strong communication, data analysis skills, and experience with clinical research and drug development. Excellent collaboration and leadership abilities are essential for success in this fast-paced environment.

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