Sr. Regulatory Affairs Scientist

Tunnell Government Services, Inc.; Bethesda (MD); Hybrid; USD 110,000 - 170,000; Full time

Job summary

Tunnell Government Services, Inc. in Maryland seeks a Sr. Regulatory Affairs Scientist to lead regulatory strategy for FDA submissions and guide risk mitigation across programs.

You will act as primary FDA contact, coordinate regulatory documents, maintain product profiles, and support clinical trial registrations. Requires US citizenship or Green Card; hybrid on-site two days/week in Frederick area.

Qualifications

• US citizen or lawful permanent resident required.
• Experience leading regulatory strategy for FDA submissions.
• Familiarity with FDA CDER, CBER, and CDRH processes.

Responsibilities

• Provide regulatory strategy and risk mitigation for assigned projects.
• Lead regulatory submissions planning and coordination for EDMS submissions.
• Serve as primary FDA contact and manage regulatory communications.
• Develop and maintain Target Product Profiles and regulatory documents.
• Ensure ClinicalTrials.gov entries and data quality per requirements.

Job description

Tunnell Government Services, Inc., is comprised of the industry’s leading scientists, medical and technical experts, and human capital and organizational development professionals. We approach all projects as a team and are committed to helping our clients transform and quickly achieve strategic goals.

If you are interested in joining an employee‑owned company that develops and implements innovative, integrated and differentiated solutions, please click on the links below to find the job that is right for you and contact us.

Title

Sr. Regulatory Affairs Scientist

Location

Fredrick, MD (Hybrid- two days a week on‑site)

The Contractor shall ensure compliance with FDA Sponsor responsibilities, serve as a subject matter expert for regulatory strategy including identifying and mitigating risk, and providing support to integrated project teams and working groups for submissions to and communications with the Center for Drug Evaluation and Research, Center for Biologics Evaluation and Research, and Center for Devices and Radiological Health submissions. Regulatory Affairs support includes but is not limited to the following:

• Provide subject matter expertise on all regulatory matters related to assigned regulatory projects; ensure ORA leadership and the sponsor’s representative are kept current on the progress of the program through periodic reports
• Provide regulatory support to an integrated product team or working group, which includes working with the team members, advising the team on any FDA‑related activities and issues, and attending meetings, updating ORA leadership and the sponsor’s representative through routine reports
• Lead the development of a written regulatory strategy and provide to the Government The strategy shall describe the regulatory pathway for FDA regulatory approval/licensure/clearance, any possible post‑marketing commitments, and shall also describe the target product profile or equivalent that can be used throughout the development process that will describe how a product will be utilized by the end user and provide to the Government.
• Create or provide input to and maintain Target Product Profiles and provide to the Government. The target product profiles shall contain the indication and usage, dosage and administration, dose forms and strengths, contraindications, warning and precautions, safety adverse reactions and drug interactions, use in specific populations, drug abuse and dependence/overdose, description of drug, clinical/pharmaceutical, pre‑clinical toxicology, clinical studies, references, storage and handling, patient counseling, risk evaluation mitigation strategy, and supporting documentation and/or templates as appropriate.
• Identify and mitigate regulatory risk through a project Risk Register.
• Serve as the primary contact with the FDA for assigned products; review, analyze, and respond to FDA communications and meetings by the regulatory deadline and maintain meeting minutes in EDMS.
• Coordinate, prepare, write, review, obtain, maintain, and archive the required documents for regulatory submissions in EDMS.
• Participate and represent as regulatory subject matter expert in on‑site visits at the industry partner manufacturing facility as requested
• Provide regulatory assistance for Quality Management System assessments done at the manufacturing facility performed by ORA or external consultants
• Assist in writing and/or reviewing abstracts, papers, and publications, which shall be written in collaboration with the study team members and submitted to all appropriate approval authorities
• Enter information in ClinicalTrials.gov for clinical studies prior to study initiation. Provide quality assurance for the data and information entered, and ensure compliance with the current regulatory, DHA, and ORA requirements to include upload of required documents, record verification at least once every 6 months, and updates within 30 days for changes to recruitment status, sponsor IRB, approval etc. Enter clinical study results NLT 12 months after the study’s primary completion date.
• Review and provide written critical regulatory feedback on acquisition milestone decision briefings, progress reviews, and other acquisition documents.
• Possess a Regulatory Affairs Certification (RAC)

Must be a US Citizen or full Green Card holder.

Tunnell strives to hire and retain the most qualified talent. We believe that having employees with different backgrounds and capabilities contributes to the success of our business. To attract qualified applicants, Tunnell posts to a wide variety of job sites. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Please be advised that certain client contracts may outline specific requirements for onsite work. Tunnell employees and/or contractors are expected to comply with all client requirements, including any safety and health protocols.