Associate I, Clinical Pharmacology Scientific Support & Reporting

📋 Description

• Prepare scientific reports and presentations related to clinical trials using available software
• Assists in constructing phase 1 clinical study planning documents, and writes Phase 1 protocols.
• Comply with procedures set forth in relevant IQS documents and Study protocols
• Comply with the directives issued by the management regarding clinical studies.
• Commit to producing work of the highest quality
• Pay close attention to detail

🎯 Requirements

• Bachelor’s degree, in Science, related to Field with +2 years’ experience in pharmaceutical
• Associates degree/RN with 6+ years of experience in pharmaceutical industry may be additionally
• Must possess good oral and written communication skills
• Ability to use computer to generate reports, analyze data, and create presentations
• Previous experience may be narrowly-focused or limited.
• Ability to identify opportunities and participate in process improvement initiatives.

🎁 Benefits

• paid time off (vacation, holidays, sick)
• medical/dental/vision insurance and 401(k) to eligible employees
• short-term incentive programs