Regulatory Intelligence Specialist

Regulatory Intelligence Specialist Tailored Management - 3.6 South San Francisco, CA Job Details Contract $18.00 - $34.06 an hour 13 hours ago Benefits Health insurance Dental insurance Vision insurance Qualifications Optimizing workflow processes Performance dashboard reports Data integrity assurance Document compliance management Dashboard development Knowledge management Database maintenance Data analysis reporting Data validation techniques Monitoring compliance data AI tools proficiency Drug regulation Dashboard creation support Mid-level Regulatory legal research Data integrity and documentation Continuous improvement Data quality monitoring Quality control Compliance documentation Intelligence analysis Cross-functional collaboration Ad-hoc reporting Healthcare data reporting Cross-functional communication Quality data entry FDA regulations Audit support Conducting policy research

Full Job Description Position:

Regulatory Intelligence Specialist Location:

1 DNA Way, South San Francisco, CA 94080

Duration:

12-Month Contract (Potential Extension or Conversion to Full-Time)

Compensation:

$18.00 - $34.06/hr on W2

Benefits:

Weekly Pay, Medical, Dental, and Vision Coverage Position Overview We are seeking a detail-oriented and proactive Regulatory Intelligence Specialist to support the Regulatory Intelligence function through research, analysis, and operational support activities. This role is responsible for monitoring changes in the global regulatory landscape and ensuring timely communication of relevant insights to internal stakeholders. Key Responsibilities Monitor and track global regulatory developments, including health authority guidance updates, policy changes, and compliance requirements from agencies such as FDA, EMA, and other international regulatory bodies Conduct research using health authority websites, industry publications, databases, and other regulatory intelligence sources Collect, analyze, filter, and prioritize regulatory information relevant to ongoing development programs Prepare clear and concise regulatory intelligence summaries, reports, and briefings for cross-functional teams Track competitor regulatory activities, including product approvals, submissions, label updates, and pipeline developments Maintain and update regulatory intelligence databases, trackers, and knowledge management systems such as Veeva Vault or similar platforms Perform data entry, validation, and quality control checks to ensure data accuracy and completeness Organize and standardize regulatory information for efficient reporting and accessibility Support development and maintenance of dashboards, trackers, and reporting tools for leadership visibility Respond to ad hoc regulatory intelligence requests from internal stakeholders Collaborate with Regulatory Affairs, Clinical, and Program Management teams to align intelligence activities with business needs Ensure documentation is audit-ready, compliant, and properly maintained Identify process improvement opportunities and recommend enhancements to existing workflows and systems Utilize AI and digital tools, where applicable, to improve efficiency in data collection, summarization, and reporting Effectively manage multiple priorities and deadlines within a fast-paced, highly regulated environment #TMN