Manager, RA Submissions

Job title:

Manager, RA Submissions

Company

Johnson & Johnson

Job description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.comJob Function:
Regulatory Affairs GroupJob Sub Function:
Regulatory Product Submissions and RegistrationJob Category:
ProfessionalAll Job Posting Locations:
High Wycombe, Buckinghamshire, United KingdomJob Description:About Innovative MedicineOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.Learn more at https://www.jnj.com/innovative-medicineWe are searching for the best talent for a Manager, RA Submissions. This hybrid work position will be located in High Wycombe, UK. The position will manage Clinical Trial Applications as a member of the Next Generation Submissions (NGS) organization.Key Responsibilities:

• Be responsible for the submission, operational management, and delivery of regulatory submissions at a compound level to support global development and registration, primarily focused on Clinical Trial Applications (CTAs).
• Create and handle dossier plans/submission packages in line with regulatory strategy, seeking input from regulatory therapeutic areas, functional area representatives, and vital collaborators, while providing guidance to project team members.
• Contribute to decisions that have an impact on the quality and timeliness of moderate to sophisticated Health Authority submissions.
• Make decisions on submission operational strategies for the best project management approach within process/timeline/resource constraints.
• Lead Submission Team meetings to coordinate the preparation and maintenance of regulatory submissions and filings.
• Take a leadership role for the monitoring and efficiency of the submission process and initiate changes within the scope of decision-making authority to minimize inefficiencies and ensure / improve quality.
• Cultivate effective relationships, maintaining open communication with key partners to ensure priority conflicts, resource issues, and deviations from the plan are identified and resolved.
• Develop departmental work practices, process enhancements / improvements, and associated training materials.
• May be responsible for performance and development of direct reports.

Qualifications:Experience and skills:Education

• University/bachelor’s degree and 6 years of related professional experience.
• Masters/PharmD/PhD in combination with 4 years of relevant/related professional experience.

Required:

• University/bachelor’s degree and 6 years of related professional experience, or
• Masters/PharmD/PhD in combination with 4 years of relevant/related professional experience.
• In-depth understanding of drug development process.
• Ability to demonstrate in-depth knowledge of regulatory submissions, filings, and processes.
• Ability to work and lead in a matrix environment.
• Proven ability to build positive relationships and influence collaborators across an organization.
• Proficiency in relevant submission-related Health Authority and Industry regulations and guidelines.
• Proficient use of Regulatory Information Systems.
• Fluency in English; other languages may be required depending on assignment.
• Validated project or submission management capabilities.
• Previous experience leading Submission Team meetings to coordinate the preparation and maintenance of submissions and filings.

Preferred:

• At least 5 years of Regulatory Affairs experience.
• Experience associated with leading EUCTR Clinical Trial Applications.

Other:

• May require up to 5% travel, domestic and international.

Please note that this role is available across multiple countries and may be posted under different requisition numbers to follow local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s):Leiden, Netherlands and Warsaw, Poland – Requisition Number: R-017237Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Expected salary

Location

High Wycombe, Buckinghamshire

Job date

Sat, 05 Jul 2025 22:24:22 GMT

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