Global Regulatory Submissions Lead Remote

Eliassen Group; Boise (ID); On-site; USD 185,976,000 - 214,906,000; Full time

Benefits offered by this job

Medical, Dental, Vision benefits

401k with company matching

Life insurance

Job summary

Eliassen Group is seeking a Regulatory Operations Project Manager to lead global eCTD submissions planning and management for high-profile molecules. This remote, contract role focuses on Modules 1-5 and coordination across U.S.

and international regions, reporting to the Head of Regulatory Operations Clinical and Publishing. The role requires 7+ years in pharma regulatory operations and strong PM skills, with experience in Veeva Vault RIM and secondary publishing support.

Qualifications

• 7+ years of direct regulatory experience in pharma with strong clinical Regulatory Operations background.
• Global eCTD submission planning and management across Modules 1-5 and regions including US, EU, and Canada, with working knowledge of ICH guidelines.
• Experience with Veeva Vault RIM.
• Strong project management skills.
• Knowledge of drug development processes and regulatory or business strategies and plans.
• Effective written, spoken, and presentation communication.
• Demonstrated teamwork and adaptability to diverse interpersonal styles.
• Ability to provide secondary publishing support for eCTD submissions when required.

Responsibilities

• Serve as the regulatory operational lead for registration planning and execution, including planning sessions, status updates, team operations meetings, and department planning.
• Lead registration management by applying expertise in electronic submission regulations, guidance, and technical content for global submissions across all CTD modules and submission types, including Ad Promo, INDs, NDA, BLAs, NDSs, MAAs, renewals, and variations.
• Partner with global teams to incorporate local agency regulations and requirements and to plan and execute submissions in regions adopting eCTD specifications.
• Guide and influence development teams regarding internal and agency registration management processes and requirements.
• Own registration management at the molecule or project level, ensuring electronic records are timely, complete, and accurate, including tracking submission status, commitments, and regulatory communications.
• Own routine compliance submissions and processes for assigned molecules, including DSUR, NDA/BLA annual reports, PSUR/PADER, and routine maintenance submissions.
• Partner with Regulatory Coordinators or Scientists to drive product deletion, divestiture, IND inactivation or withdrawal, and product withdrawal processes.
• Support secondary publishing as needed by retrieving, publishing, and submitting Modules 1-5 content per content plans, including CRFs, datasets, literature references, periodic reports, and post-marketing supplements and amendments.

Skills

Regulatory operations

Global eCTD

Veeva Vault RIM

Project management

Drug development knowledge

Communication skills

Team collaboration

Secondary publishing

Education

BS in chemistry/biology/pharmacy

Job description

Eliassen Group is seeking a Regulatory Operations Project Manager to lead global eCTD submissions planning and management for high-profile molecules. This remote, contract role focuses on Modules 1-5 and coordination across U.S.

and international regions, reporting to the Head of Regulatory Operations Clinical and Publishing. The role requires 7+ years in pharma regulatory operations and strong PM skills, with experience in Veeva Vault RIM and secondary publishing support.