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Johnson & Johnson

DCM Snr Analyst

Reposted Yesterday
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In-Office
High Wycombe, Buckinghamshire, England, GBR
Senior level
In-Office
High Wycombe, Buckinghamshire, England, GBR
Senior level
The DCM Senior Analyst oversees operational activities in the Distribution Configuration Management team, manages requests, mentors junior staff, collaborates with partners, and improves processes to ensure compliance with safety regulations.
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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 jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Product Safety

Job Sub Function:

Drug & Product Safety Operations

Job Category:

Professional

All Job Posting Locations:

High Wycombe, Buckinghamshire, United Kingdom

Job Description:

We are searching for the best talent for a Distribution Configuration Management (DCM) Analyst. This hybrid work position will be located in High Wycombe (during 2026 the office will move to Maidenhead) , United Kingdom.

Responsible for execution and oversight of operational activities within the Distribution Configuration Management (DCM)  team , including management of Distribution Anchor (DA)requests (new/modification of existing), and providing support to junior members of staff (as needed). The DCM Senior Scientist will also participate in collaborations with internal and external business partners and assist with updates to procedural documents, be involved in process improvement, metrics collection and training / mentoring of staff in DCM. The DCM Senior Scientist liaises with staff in Global Medical Safety Operations (GMSO) functions (Global Case Receipt,  Global Case Processing, Global Safety Reporting) .

Responsibilities include:

    Provide supervision and oversight for day to day and end to end activities of the Distribution Configuration Management (DCM) Team

·       Performs Distribution Anchor related activities.

·       Leads interactions with Local Safety Officers to gather regulatory requirements to support Distribution Anchor configuration and maintenance.

·       Documents local country regulatory requirements and interprets requirements into Distribution Anchor technical requirements.

·       Creates Distribution Anchors directly into the Global Safety system.

·       Performs Quality Control activities of individual and team related work.

·       Performs User Acceptance Testing of new/modified Distribution Anchors  as required.

·       Deputizes for Manager/Director as identified.

·       Workload oversight and Team Leadership

·       Manages the daily workload and ensures tasks are allocated as required.

·       Takes the lead in team meetings and daily liaison with team members to identify and resolve issues.

·       Prepares agendas, facilitates team meetings and takes minutes.

·       Flags resourcing or operations concerns to manager/director in timely manner.

·       Takes the lead and drives the creation and continuous improvement of consistent processes that meet both internal and regulatory standards to ensure global compliance.

·       Assists Manager/Director with implementation of processes, and issue management.

Liaises with technical vendors supporting the Global Safety System 

Minimum Qualification Education:
  • Degree and/or relevant work experience, advanced degree is preferred

Required Experience

  • Developed Understanding of US and EU electronic regulatory reporting requirements for ICSRs.

  • Accumulated expertise in pharmacovigilance operations related activities including single case processing, database queries, expedited reporting.

  • Knowledge of regional and global safety regulations

  • Good understanding of technologies, systems and databases related to E2B electronic reporting.

  • Highly reliable, and compliant with legal and company guidelines

  • Excellent organizational and communication skills including presentation abilities.

  • Ability to produce high quality work under time critical and high-pressure situations.

  • Project Management Skills desirable



Required Skills:



Preferred Skills:

Top Skills

E2B Electronic Reporting

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