Submissions Fellowship 2026

A Fellowship at HHN is an entry-level position designed to provide a foundational understanding of health and wellness advertising, the company, and the specific department. This role emphasizes training and development, offering access to courses such as Pharma 101, Business Writing, and Foundations of Presenting.

Fellows will also participate in executive-led discussions to gain insight into how departments collaborate to serve clients. The program offers a unique opportunity to build your professional network and receive mentorship from leaders in pharmaceutical advertising.

The Submissions Fellow ensures that projects are compliant and error-free for submission to the client’s medical, legal, and regulatory review panel to reduce turnaround. The Submissions Fellow will gain expert knowledge of clients’ regulatory submission platforms, tools, and processes to guide the internal Havas team on project submissions to ensure that projects are submitted correctly and on time.

Candidates selected to move forward will complete a brief video interview via HireVue. This recorded interview can be completed online using any device with a webcam.

Fellows are required to work on a hybrid basis from one of our offices in New York, NY or Boston, MA. Please note that Havas Health does not provide relocation assistance, housing, or reimbursement for moving expenses.

RESPONSIBILITIES

• Prepare and review documents for each asset to be submitted to the client’s regulatory, medical, and legal teams, ensuring compliance.
• Upload all assets, annotations on medical claims, reference documents, metadata, and supporting documents into the client’s regulatory platform.
• Coordinate with the internal Havas team to create submission timelines for all assets and ensure adherence to established timelines.
• Review tagging and linking of references in the submission platform for accuracy.
• Serve as the primary contact for questions related to submission requirements and guidance.
• Provide support and file management on the client’s regulatory platform.
• Track job routings and provide feedback from the Medical, Legal, and Regulatory (MLR) reviewers to the project team.
• Track reference IDs and asset codes.
• Perform quality control checks.
• Handle administrative and ad hoc assignments as instructed by the supervisor.

IDEAL EXPERIENCE

• Bachelor’s degree (BA/BS) in Marketing, Communications, Business Administration, Health Science, or equivalent.
• 0-1 year of experience in pharmaceutical advertising with knowledge of the regulatory review process, healthcare, or communications industry.
• Demonstrated proficiency in MS Suite, Excel, and Adobe Acrobat.
• Comfortable working in a fast-paced environment.
• Ability to work under pressure while maintaining high-quality work standards.
• Adaptability, fast learning, strong organizational skills, multitasking abilities, and exceptional attention to detail.

COMPENSATION

• $55,000 + Overtime (non-exempt)