Senior Associate, Clinical Pharmacology Scientific Support  Reporting Writing

📋 Description

• Prepare scientific reports and presentations for clinical trials
• Assist in phase 1 study planning documents and protocols
• Review clinical protocols and key decisions impacting timelines
• Analyze clinical study data and perform blinded safety/efficacy reviews
• Maintain scientific integrity and document conventions
• Mentor Therapeutic Area personnel and participate in process improvement

🎯 Requirements

• Bachelor’s/Master’s in a science field with 7+ years in pharma
• Understanding of clinical study principles
• Strong oral and written communication
• Proficient in analyzing data, generating reports, creating posters
• Knowledge of complex analyses, leadership, and project management
• Experience supporting clinical research and drug development

🎁 Benefits

• Comprehensive benefits package
• Paid time off and 401(k) program
• Short-term incentive eligibility