Senior Associate, Trial Disclosure

📋 Description

• Completes writing activities to assist in ensuring timely disclosure of accurate, consistent
• Provides medical writing expertise for multiple compounds and/or projects within a therapeutic area.
• Operationalizes changes in regulatory requirements via participation in the development and
• Communicates deliverables, writing process and timelines effectively across functional areas and
• Coordinates the review, approval, and other appropriate functions involved with the registration
• Accountable for completing the assigned studies within established timelines and with an

🎯 Requirements

• Bachelor's degree (BA/BS) from an accredited college or university is required, preferably in a
• 3-4 years experience in clinical trial registries, regulatory agency transparency or drug
• Relevant industry experience in medical writing in the healthcare industry or academia preferred
• 1-3 years of writing experience preferred
• Knowledge of generally accepted project management practices
• Demonstrated success in managing broad scope projects involving cross-functional teamwork

🎁 Benefits

• Paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance
• 401(k)
• Short-term incentive programs