Manager, RA Submissions

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.com

Job Function:
Regulatory Affairs Group

Job Sub Function:
Regulatory Product Submissions and Registration

Job Category:
Professional

All Job Posting Locations:
Allschwil, Basel-Country, Switzerland

Job Description:

Our 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-medicine

Johnson & Johnson is recruiting for a Manager, RA Submissions.

The position is located Switzerland.

The position will manage Clinical Trial Applications as a member of the Next Generation Submissions (NGS) organization.

Key Responsibilities:


* Be responsible for the operational management and delivery of global clinical trial regulatory submissions.


* Create and handle dossier plans/submission packages in line with clinical trial regulatory strategy,


* Support decision making impacting the quality and timeliness of Clinical Trial Health Authority submissions


* Make decisions on clinical trial submission operational strategies for the best project management approach within process/timeline/resource constraints.


* Lead Clinical Trial 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:


* 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 cl...