Medical Affairs Tender Evidence Manager
Added 25 Aug · still live
Not disclosed
Salary
Not disclosed by employer
£48,200
Going rate
Skilled Worker going rate
This role likely qualifies for a Skilled Worker visa
SOC 2482 (75% match) is an eligible occupation, with a going rate of £48,200, and Johnson & Johnson MedTech is a licensed sponsor. That is our reading of the rules. Whether they issue a Certificate of Sponsorship is still their call.
This could also be SOC 2161 (Research and development (r&d) managers, Manages tender clinical evidence process and scientific excellence across region). We read the code off the advert, so it is our best guess, not the employer's.
About the role
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
Medical Affairs Group
Job Sub Function
Medical Affairs – Marketed Products
Job Category
People Leader
All Job Posting Locations:
Leeds, West Yorkshire, United Kingdom
Job Description
DePuy Synthes is recruiting for a Medical Affairs Tender Evidence Manager DS EMEA, located in Leeds, UK, Pomezia, Italy, and Hamburg, Germany.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific countrys that align with your preferred locations:
St. Anthony's Road, Leeds, UK - Requisition Number: R-093344
Pomezia, Italy and Hamburg, Germany - Requisition Number: R-094052
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
In a highly tender-driven commercial EMEA region, the function of Manager Scientific Excellence is crucial to assure the delivery of timely, optimal, customized, and compliant tender clinical evidence packages fulfilling the individual tender request, and assure the highest number of quality points are awarded to the DePuy Synthes submissions. Therefore this role will manage the full tender clinical evidence process across the region and emphasize the scientific and clinical strengths of the company products.
Furthermore, this role is focused on providing medical and scientific information related to the safety and efficacy of the DePuy Synthes portfolio to healthcare professionals, and healthcare institutions.
The role reports to the Director, Medical Affairs, UK/Northern Europe and is part of the DePuy Synthes EMEA Medical Affairs team.
This role will manage amongst others EMEA Medical Affairs Specialist Scientific Excellence, and is accountable for conducting effective performance management.
This role will facilitate cross-functional collaboration with other functions, such as Medical, Clinical, HEMA & commercial on the commercialization efforts for pipeline and marketed products.
Main Duties And Responsibilities
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
Medical Affairs Group
Job Sub Function
Medical Affairs – Marketed Products
Job Category
People Leader
All Job Posting Locations:
Leeds, West Yorkshire, United Kingdom
Job Description
DePuy Synthes is recruiting for a Medical Affairs Tender Evidence Manager DS EMEA, located in Leeds, UK, Pomezia, Italy, and Hamburg, Germany.
Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific countrys that align with your preferred locations:
St. Anthony's Road, Leeds, UK - Requisition Number: R-093344
Pomezia, Italy and Hamburg, Germany - Requisition Number: R-094052
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
In a highly tender-driven commercial EMEA region, the function of Manager Scientific Excellence is crucial to assure the delivery of timely, optimal, customized, and compliant tender clinical evidence packages fulfilling the individual tender request, and assure the highest number of quality points are awarded to the DePuy Synthes submissions. Therefore this role will manage the full tender clinical evidence process across the region and emphasize the scientific and clinical strengths of the company products.
Furthermore, this role is focused on providing medical and scientific information related to the safety and efficacy of the DePuy Synthes portfolio to healthcare professionals, and healthcare institutions.
The role reports to the Director, Medical Affairs, UK/Northern Europe and is part of the DePuy Synthes EMEA Medical Affairs team.
This role will manage amongst others EMEA Medical Affairs Specialist Scientific Excellence, and is accountable for conducting effective performance management.
This role will facilitate cross-functional collaboration with other functions, such as Medical, Clinical, HEMA & commercial on the commercialization efforts for pipeline and marketed products.
Main Duties And Responsibilities
- Responsible for the tender clinical evidence process in EMEA;
- Ensuring tender submissions receive the best possible clinical evidence package in a timely fashion.
- Identifying and reviewing scientific literature to aid the products’ evidence packages.
- Ensuring copy approval and copy right compliance.
- Advice management on critical issues, provide insights on proactive tender shaping.
- Highlight evidence gaps upstream to global Medical Affairs.
- Maintain relationships with (global) departments for further streamlining of process.
- Act as DePuy Synthes EMEA first point of contact for tender clinical evidence.
- Facilitating close collaboration between Medical, Clinical, HEMA & commercial teams to drive success.
- Assure awareness and tender readiness, coordinate training.
- Support of medical-scientific projects for EMEA DePuy Synthes marketing teams around evidence based medicine (EBM) and evidence based selling (EBS).
- Coordinating and responding to all medical and scientific inquiries from medical staff and patients;
- Across the full product portfolio, in EMEA region.
- Liasing with the appropriate (global) Subject Matter Experts
- Document inquiries and responses accurately and completely in our global system according to the relevant SOPs and Work Instructions
- Ensure critical issues are escalated appropriately
- Maintain related EMEA SOPs and Work Instructions
- Training and communication on the MedInfo processes in EMEA countries, to drive further adoption.
- Responsible for managing operational aspects of the team (e.g., workflow, performance, and compliance), as well as ensuring achievement of team goals within established timelines and budgets.
- Presents to, and partners with, Medical affairs leadership and business leaders and provides insights and successes (using reports, metrics, other).
- Responsible for communicating business related issues or opportunities to next management level
- Finished BSc or MSc degree in relevant area such as Biomedical science or related, resulting in knowledge and understanding of:
- Human Physiology and Anatomy
- High level of scientific understanding
- Evidence based medicine, scientific and clinical research terminology
- Minimum of 1-3 years of prior work experience in comparable role
- Fluent in English (written and spoken) and strong communication skills across multiple media
- Business proficiency in additional language(s) is a distinct advantage.
- Demonstrable time management and organizational skills
- Very independent with a proactive approach to finding solutions and problem solving
- Proven experience in evidence evaluation and communication
- IT-skills (MS office)
- Self-motivation and independence
- High level of accuracy and attention to detail
- Detail-and process oriented.
- Understanding of compliance, privacy and confidentiality
- Excellent research skills and highly analytical
- Adaptable and able to work with a wide range of different personalities
- Networker and flexible and adaptable team player
- Able to prioritise and manage workload autonomously
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.
#DePuySynthesCareers
Required Skills
Preferred Skills:
Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Developing Others, Healthcare Trends, Inclusive Leadership, Leadership, Medical Affairs, Medical Communications, Medical Compliance, People Performance Management, Product Strategies, Program Management, Scientific Communications, Strategic Thinking
Analytical Reasoning, Clinical Research and Regulations, Clinical Trials Operations, Communication, Developing Others, Healthcare Trends, Inclusive Leadership, Leadership, Medical Affairs, Medical Communications, Medical Compliance, People Performance Management, Product Strategies, Program Management, Scientific Communications, Strategic Thinking
This description is the source posting as it read when we added it. We are not affiliated with Johnson & Johnson MedTech, so check their own site for the current details.
Where this offer sits in the market
SOC 2482 · UK · ONS ASHE 2025 · ~137k in sampleP25 £40kP75 £66k
£33kmedian £50kgoing rate £48k£84k
Similar sponsored roles
See all UK visa jobsNo close matches live right now.
Browse more sponsored jobs at Johnson & Johnson MedTechAbout sponsorship for this role
Does this job guarantee visa sponsorship?
Not necessarily. Johnson & Johnson MedTech holds a sponsor licence, but sponsorship for a specific hire is always the employer's decision. Be upfront in your application that you'll require it.
What salary is needed for this role to be eligible?
The offer must clear both the general threshold and the SOC 2482 going rate of £48,200. New-entrant and shortage discounts can lower it.