Senior Associate, Trial Disclosure

Role: Senior Associate, Trial Disclosure, providing medical writing support for clinical trial registration, results postings, and regulatory disclosures across multiple therapeutic areas. Responsibilities include preparing accurate and timely scientific study summaries, protocol/results lay summaries, and supporting agency disclosure activities, including redaction and anonymization of clinical documents. The role involves coordinating with cross-functional teams, implementing SOPs to adapt to regulatory changes, and managing complex registration projects, including non-interventional safety studies. Qualifications: Bachelor's in health or biological sciences; 3-4 years of experience in clinical trial registries, regulatory disclosures, or drug development; industry experience in medical writing preferred, with AMWA certification or similar advantageous. Skills include strong project management, scientific content interpretation, and global registration requirements knowledge, with proficiency in tools like Excel and Word. High-value specifics: focus on transparency, global registry compliance, and regulatory disclosure processes within biopharma, supporting multiple therapeutic areas with complex study designs. Work setup and travel details are not specified.