Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing

Role Summary

Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing. Hybrid opportunity requiring onsite 3x/week in Lake County, IL. Responsible for building data and information for internal documents and scientific reports related to clinical trials, and ensuring multiple reports progress through multitasking.

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, study protocols, and directives regarding clinical/preclinical studies.
• Analyze clinical study data, including statistical data, to assist with blinded efficacy and safety reviews and ensure scientific integrity of processes.
• Receive and complete tasks from Therapeutic Area MD or Scientific Staff within timeline with minimal supervision.
• Ensure scientific integrity of processes by applying electronic document conventions consistently and accurately.
• Integrate clinical trial data across studies, identify issues, and communicate findings to internal peers and therapeutic area management.
• Perform literature/competitive intelligence searches to recognize/resolve scientific and technical problems using current document conventions.
• Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management.
• Maximize individual, therapeutic area and team productivity; mentor therapeutic area personnel.

Qualifications

• Bachelors/Master‚Äôs degree in Science related field with 7+ years‚Äô experience in the pharmaceutical industry.
• Understanding of clinical study principles.
• Good oral and written communication skills.
• Proficiency in analyzing clinical study data, generating reports, and creating presentations, posters and manuscripts.
• Knowledge of complex scientific analyses, business-related procedures, and project leadership.
• Experience supporting clinical research, drug development and/or therapeutic area operations.
• Proven record of successful projects.
• Attention to detail and ability to produce high-quality work.
• Ability to use resources effectively to complete tasks and meet timelines.
• Independent expertise to analyze clinical study/statistical data using available software.

Skills

• Clinical data analysis
• Scientific reporting and writing
• Phase 1 protocol development
• Statistical data interpretation
• Electronic document management
• Cross-functional collaboration

Education

• Bachelors or Master's degree in a science-related field

Additional Requirements

• Onsite 3x/week in Lake County, IL