Field Clinical Specialist Crm Rennes jobs at Boston Scientific in France

France-Centre-Val de Loire

About the Role
The Field Clinical Specialist (FCS) provides field/remote clinical, technical and educational support to assigned accounts at a Territory, Regional, National or EMEA level.

Working with the Cardiac Rhythm Management (CRM) portfolio, this role covers Limoges, the South West of France, with some additional case support as and when required by client needs. Work is driven by Customer demand and pre-planned support requirements, and the primary focus is case support, using clinical expertise to influence Customer usage of the full portfolio.

This remote field-based role offers a permanent position and requires extensive travel across Limoges, the South West of France (up to five days per week).

Your responsibilities will include:

• Act as a primary resource forclinical support in the areas of case coverage and basic troubleshooting for company products.
• Work is driven by Customer demand and pre-planned support requirements and may require occasional weekend work.
• Attend cases in-person/remotely with our customers and advise physicians on clinical attributes/techniques associated with our products.
• Ensure timely collection and reporting of all required medical documentation pertaining to our procedural device operation.
• Support the team to achieve projected sales goals and increase sales revenues.
• Develop a deep understanding on the workflows and specificities of each hospital and business relationships with healthcare personnel (e.g. through informal conversation, meetings, participation in conferences) to make new contacts in hospital departments and to identify key decision makers.
• Respond to complex customer needs and complaints regarding products and service by developing creative and feasible solutions or working with other related personnel (e.g., sales, clinical, research, marketing, technical support) to develop optimal solutions.
• Record customer information and activities in company’s CRM system: use the system as an alignment tool with other commercial roles.
• Provide education support on product usage and customer training.

• In this role, you will be responsible for Bordeaux, the South West and West of Franceandmay on occasion be required to support colleagues in neighboring regions.
• This remote field-based role requires frequent weekly travel acrossSouth West and West of France

What are we looking for in you:

• Clinical experience within Cardiac Rhythm Management (e.g., as a Field Clinical Specialist, Cardiac Physiologist, or similar) is beneficial.

• Successfully completed degree studies (or equivalent) within Biomedical Sciences or healthcare subject is beneficial.

• Strong communication skills.
• Can understand and communicate complex technical and clinical details.
• Can rapidly adapt to a very dynamic marketplace.
• Strong team player, collaborative, can build relationships and work cross-functionally.
• Self-motivated and can influence others.
• Flexible, adaptable but focused and persistent.
• Willing and can travel extensively as required by workload.

• Professional working proficiency (or above) language skills in both French and English.

What we can offer to you:

• Experience in a groundbreaking multinational company with attractive benefits.
• Inspirational colleagues and culture.
• Career development.
• Fast growing and innovative environment.
• A company team culture.
• International opportunities.
• Excellent training/development programs.
• A permanent position.
• A remote field-based role.

Costa Rica-Coyol

About the Role:

To support the plant facilities operations and give support on quality records such as cleaning records, pest control, maintenance reports, etc

You’re Responsibilities Include:

• Ensure that the entire facility or plant is operating effectively and efficiently.
• Review and keep track on quality records such as cleaning records, pest control, maintenance reports, etc
• Supervision of our facilities services, specifically the cafeteria, transportation, and cleaning operations, during shifts B and C
• Assisting in Budgeting and cost control on projects and maintenance.
• Schedule utilities equipment and building maintenance activities.
• Gives technical guidance (supervise) to facilities technicians and contract personnel. Interface with various vendors that support the plant and its operating systems
• Keep track of CEWN permits, as part of this tracking, the Facilities Trainee/coordinator shall assign consecutive number, route them for signatures and proper communication of the job completion. In addition to that, the Facilities Trainee/ coordinator shall follow up the CEWN closure process and keep the records as a quality register.

What We’re Looking For

• Bachelor’s degree in Mechanical, Industrial Engineer or related
• English Level: 70-79%.
• Experience: At least 1 years
• Autocad.
• Computerized preventine maintenance.
• Availability to worknight shift.

Costa Rica-Heredia

Hybrid Roles:

OurInterventional Oncology and Embolization (IO&E)portfolio empowers physicians to treat tumors less invasively. It includes:

• Embolization technologies
• TheraSphere™ Y90 transarterial radioembolization
• Ablation technologies

, you will lead cross-functional teams in the execution ofin oncology. This role emphasizes agility, learning, and creative problem-solving to accelerate the development of breakthrough cancer therapies.

• Lead strategic and operational planning of interventional oncology trials
• Manage global clinical studies in alignment with strategy, budget, and SOPs
• Collaborate on development of study materials, systems, and regulatory submissions
• Engage with external physicians and key opinion leaders (KOLs)
• Oversee clinical trial budgets (up to 25%) including forecasting and variance reviews
• Direct CROs and clinical vendors
• Ensure audit readiness and risk management throughout the study lifecycle
• Present study progress, data, and risks to leadership
• Provide clinical input to product development teams
• Domestic travel: 10–25%

• Bachelor’s degree with 5+ years of oncology-related experience
• 1–3 years in early feasibility oncology clinical research
• 1–3 years of project/trial management experience
• 1–3 years of financial and budget management experience
• Experience working with CROs and clinical vendors

• Experience in solid tumor , medical device , or drug development
• Familiarity with product development teams

• Innovative thinking and problem-solving
• Strategic execution with minimal supervision
• Strong collaboration and influence across global stakeholders
• Adaptability in dynamic and uncertain environments

France-Auvergne-Rhône-Alpes; Belgium-Diegem; France-Bourgogne-Franche-Comté; France-Bretagne; France-Centre-Val de Loire; France-Grand Est; France-Hauts-de-France; France-Normandie; France-Nouvelle-Acquitaine; France-Occitanie; France-Pays de la Loire; France-Provence-Alpes-Côte d'Azur; France-Voisins le Bretonneux; France-Île-de-France; Ireland North - Belfast; Ireland North - Derry; Ireland-Clonmel; Ireland-Cork; Ireland-Craigavon; Ireland-Drogheda; Ireland-Dublin; Ireland-Dundalk; Ireland-Galway; Ireland-Kerlogu; Ireland-Kerlogue; Ireland-Limerick; Ireland-Waterford; Norway-Asker; Sweden-Helsingborg; United Kingdom-Aberdeen; United Kingdom-Ashford; United Kingdom-Backburn; United Kingdom-Barnsley; United Kingdom-Barnsley; United Kingdom-Basildon; United Kingdom-Basingstoke; United Kingdom-Bath; United Kingdom-Bedford; United Kingdom-Birkenhead; United Kingdom-Birmingham; United Kingdom-Blackpool; United Kingdom-Bolton; United Kingdom-Bournemouth; United Kingdom-Bradford; United Kingdom-Bradford; United Kingdom-Brighton; United Kingdom-Bristol; United Kingdom-Camberley; United Kingdom-Cambridge; United Kingdom-Canterbury; United Kingdom-Cardiff; United Kingdom-Carlisle; United Kingdom-Chelmsford; United Kingdom-Cheltenham; United Kingdom-Chester; United Kingdom-Colchester; United Kingdom-Coventry; United Kingdom-Crawley; United Kingdom-Darlington; United Kingdom-Derby; United Kingdom-Doncaster; United Kingdom-Dundee; United Kingdom-Eastbourne; United Kingdom-Edinburgh; United Kingdom-Exeter; United Kingdom-Farnham; United Kingdom-Glasgow; United Kingdom-Gloucester; United Kingdom-Guildford; United Kingdom-Harlow; United Kingdom-Hartlepool; United Kingdom-Hastings; United Kingdom-Hemel Hempstead; United Kingdom-Huddersfield; United Kingdom-Hull; United Kingdom-Leeds; United Kingdom-Leicester; United Kingdom-Lincoln; United Kingdom-Liverpool; United Kingdom-Maidstone; United Kingdom-Maidstone; United Kingdom-Manchester; United Kingdom-Middlesbrough; United Kingdom-Milton Keynes; United Kingdom-Newcastle; United Kingdom-Newport; United Kingdom-Northampton; United Kingdom-Norwich; United Kingdom-Nottingham; United Kingdom-Nuneaton; United Kingdom-Oxford; United Kingdom-Peterborough; United Kingdom-Plymouth; United Kingdom-Poole; United Kingdom-Portsmouth; United Kingdom-Preston; United Kingdom-Reading; United Kingdom-Rochdale; United Kingdom-Rotherham; United Kingdom-Sale; United Kingdom-Salford; United Kingdom-Sheffield; United Kingdom-Slough; United Kingdom-Solihull; United Kingdom-Southampton; United Kingdom-Southend-on-Sea; United Kingdom-Stevenage; United Kingdom-Stoke; United Kingdom-Swansea; United Kingdom-Swindon; United Kingdom-Taunton; United Kingdom-Telford; United Kingdom-Warrington; United Kingdom-Watford; United Kingdom-Western-super-Mare; United Kingdom-Woking; United Kingdom-Wolverhampton; United Kingdom-Worchester; United Kingdom-Worthing; United Kingdom-Wrexham; United Kingdom-York

the role:

As a Senior Field Clinical Engineer (FCRE) at Boston Scientific, you will play a vital role in supporting the execution and management of clinical trials and providing commercial support in the field. Your work will directly impact patient outcomes, support the advancement of medical innovation, and help bring life-changing therapies to market. In this role, you’ll serve as the clinical expert at trial sites, educate healthcare professionals, and provide hands-on technical support during procedures in hospital and clinic settings.

Clinical trial responsibilities:

• Manage clinical trial activity within your assigned territory to meet corporate and departmental objectives
• Complete site Interest Visits and Site Initiation Visits
• Educate clinical investigators on trial protocols, clinical processes, and investigational product features
• Provide technical support for clinical trial procedures including implants and follow-up visits, with direct patient contact
• Train on and maintain knowledge of clinical trial protocols, SOPs, and global regulatory compliance
• Manage investigational product inventory throughout the clinical process

Commercial responsibilities:

• Educate customers on the proper clinical usage and benefits of Boston Scientific’s commercially approved products
• Deliver presentations and product demonstrations to current and potential customers
• Develop strong relationships with hospital personnel and key decision-makers
• Address customer needs and complaints by providing timely, feasible solutions

General responsibilities:

• Support both commercial and clinical procedures, including patient implants and follow-ups
• Ensure adherence to guidelines for managing commercial and investigational product inventor

Quality system requirements:

• Demonstrate a strong commitment to patient safety and product quality by complying with the Quality Policy and all documented quality processes and procedures
• Support a work environment that fosters quality compliance (for roles involving supervision)

Required qualifications:

• Minimum of 5 years' experience in electrophysiology (EP), cardiac rhythm management (CRM), or a similar clinical/technical field
• Demonstrated ability to manage complex field activities and clinical support functions
• Strong working knowledge of clinical trial protocols and regulatory standards
• Ability to work independently and collaboratively in a fast-paced environment
• Willingness and ability to travel extensively and be on-call, including evenings and weekends

Preferred qualifications:

• Bachelor’s degree in Biomedical Engineering, Life Sciences, or related field
• Prior experience supporting implantable medical devices in a clinical setting
• Familiarity with Good Clinical Practices (GCP) and FDA/ISO regulations
• Excellent communication, presentation, and relationship-building skills
• Experience working with investigational product inventory and device logistics

France-Voisins le Bretonneux

Governance and strategy

• Represent Boston Scientific in local trade associations (e.g., SNITEM) to ensure alignment with evolving industry codes and regulations

• Chair the local compliance committee in France, driving effective governance and timely decision-making

• Lead the annual risk assessment process by partnering with the Country Leadership Team to identify and prioritize key compliance risks

• Drive the strategy and execution of Annual Country Compliance Plans, aligning initiatives with risk assessments and compliance objectives

• Track progress of key initiatives, report on compliance KPIs, and escalate material risks as appropriate

Culture and partnership development

• Partner closely with the Country Leadership Team in France to embed compliance into commercial and operational strategies

• Act as a visible compliance ambassador and business partner, fostering a speak-up culture and ethical decision-making

• Design and deliver engaging compliance training and communication programs tailored to various levels of the organization

• Collaborate cross-functionally with Legal, Commercial Divisions, HR, Finance, and other stakeholders to ensure proactive, solution-oriented compliance

• Represent France in regional and global compliance forums to share local insights and ensure alignment across business units

Operational support

• Serve as the primary point of contact for review and approval of HCP/HCO interactions in France and the EMEA Proctor Bureau

• Ensure documentation, due diligence, and approvals are compliant with internal controls, SOPs, and MedTech/local codes

• Provide expert-level advice on complex compliance scenarios, including high-risk and non-standard cases

• Deliver timely, pragmatic guidance on both local and international compliance policies (e.g., MedTech Europe Code, Anti-Gift Law)

• Monitor and drive continuous improvement of compliance systems, workflows, and internal controls

• Mentor and support junior compliance professionals and business partners to build internal compliance capabilities

Required qualifications:

• Minimum of 7 years' experience in compliance, legal, or a related field, preferably within the medical device, pharmaceutical, or healthcare sector

• Deep understanding of local and international healthcare compliance regulations, including MedTech Europe Code and Anti-Gift Law

• Proven ability to lead cross-functional initiatives and influence senior stakeholders

• Strong analytical, problem-solving, and decision-making skills

• Excellent communication skills in both English and French

• Familiarity with compliance systems and tools used in multinational organizations
• Previous experience supporting operational compliance activities or anti-bribery/anti-corruption audit activities across EMEA

N/A; France-Bretagne

TheField Clinical Specialist(FCS) provides field/remote clinical, technical and educational support to assigned accounts at a Territory, Regional, National or EMEA level.

Working with the(CRM) portfolio, this role covers fromWest Paris to Rennes, with some additional case support as and when required by client needs. Work is driven by Customer demand and pre-planned support requirements, and the primary focus is case support, using clinical expertise to influence Customer usage of the full portfolio.

This remote field-based role offers a permanent position and requires extensive travel across the area that includes West Paris and Rennes

Your responsibilities will include:

• Act as a primary resource for clinical support in the areas of case coverage and basic troubleshooting for company products.
• Work is driven by Customer demand and pre-planned support requirements and may require occasional weekend work.
• Attend cases in-person/remotely with our customers and advise physicians on clinical attributes/techniques associated with our products.
• Ensure timely collection and reporting of all required medical documentation pertaining to our procedural device operation.
• Support the team to achieve projected sales goals and increase sales revenues.
• Develop a deep understanding on the workflows and specificities of each hospital and business relationships with healthcare personnel (e.g. through informal conversation, meetings, participation in conferences) to make new contacts in hospital departments and to identify key decision makers.
• Respond to complex customer needs and complaints regarding products and service by developing creative and feasible solutions or working with other related personnel (e.g., sales, clinical, research, marketing, technical support) to develop optimal solutions.
• Record customer information and activities in company’s CRM system: use the system as an alignment tool with other commercial roles.
• Provide education support on product usage and customer training.

• In this role, you will be responsible for West Paris and Rennes area and may on occasion be required to support colleagues in neighboring regions.
• This remote field-based role requires frequent weekly travel across the North-West ofFrance(up to five days per week) based on customer needs.

What are we looking for in you:

• Clinical experience within Cardiac Rhythm Management (e.g., as a Field Clinical Specialist, Cardiac Physiologist, or similar) is beneficial.

• Successfully completed degree studies (or equivalent) within Biomedical Sciences or healthcare subject is beneficial.

• Strong communication skills.
• Can understand and communicate complex technical and clinical details.
• Can rapidly adapt to a very dynamic marketplace.
• Strong team player, collaborative, can build relationships and work cross-functionally.
• Self-motivated and can influence others.
• Flexible, adaptable but focused and persistent.
• Willing and can travel extensively as required by workload.

• Professional working proficiency (or above) language skills in both French and English.

What we can offer to you:

• Experience in a groundbreaking multinational company with attractive benefits.
• Inspirational colleagues and culture.
• Career development.
• Fast growing and innovative environment.
• A company team culture.
• International opportunities.
• Excellent training/development programs.
• A permanent position.
• A remote field-based role.