Remotely
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Job Description
📋 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
