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Location:Belgium (Remote, field-based with travel as required), ideally based between Brussels & Antwerp.
Range depends on experience, but is between ~ €90.000,- and €110.000,- including commission (20%)
Leading with purpose, advancing patient care
This is a permanent, field-based position requiring regular travel across Belgium. You will report to the Senior Supervisor, Field Clinical Specialists EP.
What you’ll be doing
In this role, you will not only manage people - but you will also shape the future of patient care by empowering a team of Field Clinical Specialists Electrophysiology to deliver world-class clinical and commercial support. Your leadership will be the bridge between our people, our customers, and the patients whose lives we impact every day.
Your responsibilities will span three core areas:
of the Field Clinical Specialist team, helping them to perform at their best and grow their careers. From attracting and onboarding new colleagues to providing feedback, setting clear goals, and tracking KPIs, you will foster a high-performing, motivated, and engaged team culture.
will be central to your success. You willclosely with Account Managers, Marketing, and other cross-functional teams to. At the same time, you will nurture strong relationships with hospitals and healthcare professionals, supporting them through training, education forums, and day-to-day partnership. Whether aligning with sales colleagues on account growth or coordinating with logistics to guarantee product availability, your ability to connect people and processes will make a tangible difference.
About you
You are an engaging (first level) people supervisor – or someone with the ambition to grow into such a role - with a passion for people. s development. Your style is structured, results-driven approach. While hands-on experience in electrophysiology or cardiac rhythm management is a plus, we welcome candidates with experience in related MedTech fields such as cardiology or structural heart. A background in biomedical engineering, life sciences, or a similar discipline is ideal.
On a practical level, you bring:
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About the role:
The Field Clinical Specialist in Neuromodulation will offer expert clinical and technical support, as well as training to physicians and sales representatives, ensuring the effective and safe use of Neuromodulation products during procedures. In particular, the main focus will be on SCS (Spinal Cord Stimulator) and RF (Radiofrequency Ablation) systems.
Your responsibilities include:
What we are looking for:
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Your responsibilities will include:
Required qualifications:
Preferred qualifications:
The anticipated annualized base amount or range for this full time position will be, plus variable compensation governed by the Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives) as well as the value of core and optional benefits offered at BSC, which can be reviewed at www.bscbenefitsconnect.com. Actual compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, and other relevant business or organizational needs.
For MA positions:It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.
Among other requirements, Boston Scientific maintains specific prohibited substance testing requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a drug test as a pre-employment requirement. The goal of the drug testing is to increase workplace safety in compliance with the applicable law.
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Your responsibilities will include:
Required qualifications:
Preferred qualifications:
The anticipated annualized base amount or range for this full time position will be, plus variable compensation governed by the Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives) as well as the value of core and optional benefits offered at BSC, which can be reviewed at www.bscbenefitsconnect.com. Actual compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, and other relevant business or organizational needs.
For MA positions:It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.
Among other requirements, Boston Scientific maintains specific prohibited substance testing requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a drug test as a pre-employment requirement. The goal of the drug testing is to increase workplace safety in compliance with the applicable law.
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Belgium-Diegem; France-Voisins le Bretonneux; Germany-Düsseldorf; Italy-Milan; Netherlands-Kerkrade; Spain-Madrid; United Kingdom-Hemel Hempstead
This is a highly dynamic role in which you will work in a team environment to develop global evidence-based clinical strategies for cardiology medical devices (Cardiac Rhythm Management) by creating clinical documentation that systematically synthesizes information from multiple data sources. As a Clinical Evaluation Scientist, you will plan and develop clinical evaluation reports (CERs) and post-market clinical follow-up (PMCF) reports, as well as summary of safety and clinical performance reports (SSCPs) in alignment with applicable clinical and regulatory standards and business needs. This role applies analytical thought processes and a highly methodical clinical evaluation approach to develop benefit/risk profiles for the Boston Scientific portfolio cardiology devices. A successful candidate has excellent writing skills as well as the ability to work collaboratively with cross-functional partners. Your efforts support product approval, indication expansion and claim support, and mandated post-market requirements.
Your responsibilities will include:
Compile, appraise, and evaluate data from multiple sources including clinical trials, medical literature, design verification/validation data, and product complaint data. Compare and align this data with Risk Documentation and product labeling to identify gaps or emergent concerns.
Develop literature search strategies in collaboration with librarians and perform methodical evaluation of medical literature including screening, appraisal and extraction of relevant data.
Develop Clinical Benefit Statements in collaboration with medical experts and develop pre- and post-market data collection strategies to support the developed statements.
Create analyses to evaluate product benefit/risk profile, safety (e.g., develop a profile of adverse events), and performance. Identify potential clinical evidence gaps and contribute to development of prospective evidence strategy to address gaps.
Develop global clinical data strategies in collaboration with leadership and cross-functional partners to support market access for New Product Development, Sustaining Product compliance and Design Changes to existing products.
Manage ongoing Design and Quality activities to support necessary changes and/or improvements to devices, including assessing the impact to existing clinical data strategies, proposing and developing new clinical data activities to meet any identified gaps, and coordinating with management to ensure resourcing needs are considered.
Aid in the development and execution of strategies for responses for regulatory submissions.
What we’re looking for in you:
Minimum Qualifications
Bachelor’s, Master’s or Advanced degree (PhD, research-based MS, MD, RN, DVM) in a scientific, medical, or engineering field.
6+ years professional experience in a scientific, engineering, medical, or medical device space
3+ years of experience inat least oneof the following: 1) Writing and Developing Clinical Evaluation Plans/Reports and Post-Market Clinical Follow-Up Plans/Reports in accordance with Regulation (EU) 2017/745 of the European Parliament (i.e., EU Medical Device Regulations), relevant Medical Device Coordination Group (MDCG) guidance, and harmonized standards; 2) Working in the clinical treatment and management of patients receiving Cardiac Rhythm Therapies, including but not limited to: Pacemakers; Implantable Cardioverter-Defibrillators (ICDs); Cardiac Resynchronization Therapy Pacemakers/Defibrillators (CRT-P/Ds); or Subcutaneous Implantable Cardioverter Defibrillators (S-ICDs) or 3) Writing, Developing, Managing, and Submitting Regulatory Technical Documentation submissions in accordance with Regulation (EU) 2017/745 of the European Parliament (i.e., EU Medical Device Regulations) to support EU Market access of Cardiac Rhythm Devices
Thorough understanding of different types of clinical evidence (e.g., literature, clinical trials, real-world evidence, etc.) and the benefits and limitations of each type of data.
Experience in strategically applying knowledge of regulations, medical knowledge, and data types to develop clinical data strategies to support submission.
Analytical skills, including strong familiarity with medical literature
Strong medical/scientific writing skills
Preferred Qualifications
3+ years of professional experience inmultipleof the areas identified above
Experience with/knowledge of with Quality Management System documentation, specifically Risk Management Documents (e.g., Hazard Analysis, Risk Management Report, Risk Management Plan)
Experience with engineering documentation, including test protocols, test reports, and international standards
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Belgium-Diegem; Denmark-Hellerup; France-Île-de-France; Germany-Düsseldorf; Italy-Milan; Netherlands-Kerkrade; Netherlands-Kerkrade; Netherlands-Maastricht; Poland-Warsaw; Spain-Madrid; US-MN-Arden Hills; United Kingdom-Hemel Hempstead
About the role:
This Manager I role provides management to assigned staff members in the Clinical organization. Through collaboration with clinical core team members, ensures clinical programs are carried out to a standard consistent with regulatory, corporate and clinical policies and procedures. This role will influence the development of policies and procedures across functions. This role contributes to and adheres to Clinical department budget. This incumbent develops and executes Clinical staffing plan. This role facilitates the appropriate resourcing of projects, programs, and staff training and development. You will ensure the clinical deliverables are of the highest standards. This incumbent also interfaces with other departments, Senior Clinical management, medical directors, senior functional management, and acts as BSC representative with CRO’s.
Your responsibilities will include:
Leads and coordinates data management activities across studies to ensure timely completion of data management deliverables (e.g., review of clinical data for completeness, accuracy, consistency, CRF/e-CRF development, database design, validation programming, and database deliverables).
Responsible for managing staff based on a combination of the number of people and the type/level of direct reports and responsible for training, mentoring, development, and supervising of clinical staff in accordance with BSC policies.
Offer advice and solutions to internal and external customers to address issues and enhance efficiency.
Develops staffing plans for the clinical functions and makes hiring decisions and leverages/allocates appropriate resources to support the clinical organization and interfaces with Project and Trial Managers / Directors and other management to develop objectives for clinical functions and to gather performance feedback.
Manages interpersonal issues and manages conflict resolutions.
Ensures that best practices of study conduct are leveraged across the clinical organization and implements process efficiencies where possible and coordinates global harmonization among staff through other clinical functional line managers.
Responsible for the provision of meaningful metrics to support the clinical organization and ensures staff is trained on the study specific materials, which include protocols, study tools, etc.
Demonstrates thorough knowledge of and ensures staff adheres to the appropriate application of clinical research conduct, laws, regulations, and standards, and compliance with applicable BSC SOPs and policies.
Interfaces as Subject Matter Expert and acts as coach and mentor with vendors performing functional tasks.
Responsible to determine, implement and execute vendor oversight activities for outsourced functional tasks.
Initiate and lead initiatives that improve efficiencies of functional processes.
Required qualifications:
Minimum bachelor’s degree, or equivalent combination of experience
Minimum 5 years with clinical data management experience
Prior experience with EDC systems, preferably Medidata Rave
Prior experience following standard operating procedures (SOP) and work instructions (WIs) in a quality environment
Prior or current experience in managing data management projects
Ability to travel up to 10% both domestic and international
Preferred qualifications:
Advanced degree in healthcare or related field preferred
Demonstrated expertise in process improvement
Ability to work effectively within a geographically diverse and global business
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In Cardiac Rhythm Management (CRM) we offer solutions for treating irregular heart rhythms and heart failure and protecting against sudden cardiac arrest. Boston Scientific develops, manufactures, and markets a broad array of products and services that enable less-invasive care for some of the most threatening cardiac conditions. We have been expanding indications and conducting pivotal research for nearly 20 years, resulting in increased access to the lifesaving and life-enhancing benefits of ICD and CRT therapies.
Your responsibilities will include:
Required qualifications:
Preferred qualifications:
The anticipated annualized base amount or range for this full time position will be, plus variable compensation governed by the Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives) as well as the value of core and optional benefits offered at BSC, which can be reviewed at www.bscbenefitsconnect.com. Actual compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, and other relevant business or organizational needs.
For MA positions:It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.
Among other requirements, Boston Scientific maintains specific prohibited substance testing requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a drug test as a pre-employment requirement. The goal of the drug testing is to increase workplace safety in compliance with the applicable law.
These jobs might be a good fit

Share
Location:Belgium (Remote, field-based with travel as required), ideally based between Brussels & Antwerp.
Range depends on experience, but is between ~ €90.000,- and €110.000,- including commission (20%)
Leading with purpose, advancing patient care
This is a permanent, field-based position requiring regular travel across Belgium. You will report to the Senior Supervisor, Field Clinical Specialists EP.
What you’ll be doing
In this role, you will not only manage people - but you will also shape the future of patient care by empowering a team of Field Clinical Specialists Electrophysiology to deliver world-class clinical and commercial support. Your leadership will be the bridge between our people, our customers, and the patients whose lives we impact every day.
Your responsibilities will span three core areas:
of the Field Clinical Specialist team, helping them to perform at their best and grow their careers. From attracting and onboarding new colleagues to providing feedback, setting clear goals, and tracking KPIs, you will foster a high-performing, motivated, and engaged team culture.
will be central to your success. You willclosely with Account Managers, Marketing, and other cross-functional teams to. At the same time, you will nurture strong relationships with hospitals and healthcare professionals, supporting them through training, education forums, and day-to-day partnership. Whether aligning with sales colleagues on account growth or coordinating with logistics to guarantee product availability, your ability to connect people and processes will make a tangible difference.
About you
You are an engaging (first level) people supervisor – or someone with the ambition to grow into such a role - with a passion for people. s development. Your style is structured, results-driven approach. While hands-on experience in electrophysiology or cardiac rhythm management is a plus, we welcome candidates with experience in related MedTech fields such as cardiology or structural heart. A background in biomedical engineering, life sciences, or a similar discipline is ideal.
On a practical level, you bring:
These jobs might be a good fit