דרושים Sr Clinical Trial Manager Oncology ב-Boston Scientific ב-צרפת

Costa Rica-Coyol

Hybrid Roles:

Your Responsibilities

• Lead projects developing high-performance solutions (including bots, automated spreadsheets, RPA (Robotic Process Automation), dashboards, data extractions, artificial intelligence, etc. Create high-quality code that satisfies needs and strives for simplicity, clarity, and testability.

• Assist in maintaining and evolving documentation, toolkits, and knowledge resources to support consistency and knowledge sharing across improvement efforts.

• Properly capture value of high-performance solutions, making delivered improvements transparent.
• Identify and recommend ways to drive more value out of the company's technology assets, maximizing reuse and avoiding redundancy. Participate in discovery sessions with business stakeholders – identifying process requirements, the solutions that can be leveraged, resources required, etc.
• Understand architectural, design, implementation, and security standards and best practices. Engage in and align practices with the company’s digital transformation strategy.

• Work closely with management to educate and to articulate the requirements necessary to promote overall digital goals.

What we are looking for

• Bachelor’s Degree or higher in engineering or data science
• 4+ years experience related to data analytics and reporting
• Knowledge in Microsoft Power Platform (Power BI, Power Automate, Power Apps)
• English level Desire 80% or above
• Please submit Resume in English

Preferred Qualifications:

• Experience in a regulated industry environment
• Working knowledge of SAP/S4Hana and Snowflake
• Proven track record of implementing strategic business initiatives in matrixed teams
• Outstanding interpersonal skills for developing relationships and driving continuous improvement

France-Île-de-France; Germany-Düsseldorf; Netherlands-Kerkrade; Spain-Madrid; United Kingdom-Hemel Hempstead

ADay in the Lifeof the EMEA Data Product Manager & Owner:

You’ll begin your day by reviewing data products performance and reliability signals across your portfolio - usage and adoption trends, data quality scores, pipeline SLAs/SLOs, and customer feedback. You’ll meet with internal customers to connect business outcomes to clear data products objectives, refining priorities to unlock measurable value.

When EMEAspecific regulatory constraints (e.g., GDPR) arise, you’ll partner with Legal, Security, and HR to chart compliant pathways that keep delivery moving.

You will work with data engineering, platform, architecture and governance teams to clarify data contracts, schemas, lineage, and access models, ensuring every increment is productionready and governed by design. You’ll groom the roadmap and backlog, decomposing epics, sharpening acceptance criteria, and balancing new capabilities with technical debt, observability, and cost optimization. You’ll demo recent increments, capture user feedback, and turn it into testable stories that improve usability, trust, and performance. You’ll brief sponsors on value realized and present investment options for the next phases.

On a monthly rhythm, you’ll coordinate with global data and architecture forums to reuse patterns, converge on standards, and ensure EMEA needs are represented in the enterprise roadmap.

As a champion of the data strategy & enablement team, you will drive adoption through excellent product experience - discoverability in the catalog, clear documentation, and dependable service levels that help teams selfserve trustworthy, governed data at scale.

The role:

Reporting to the Data Strategy & Enablement Sr Manager, the EMEA Data Product Manager & Owner is accountable endend for strategy and dayday delivery of data products

You will translate business outcomes into product capabilities, manage scope and trade

Success requires a blend of product strategy, stakeholder leadership, and handson ownership to ship secure, compliant, and scalable data products that power analytics, AI, and operational workflows across the region.

Key Responsibilities:

• Product vision & strategy: Define a 12–24‑month vision, value hypotheses, and positioning for EMEA data products, maintain an outcome‑based roadmap aligned with enterprise standards and local needs.
• Backlog ownership & delivery: Convert outcomes into prioritized epics/stories, lead refinement and planning, uphold DoR/DoD, balance features with reliability, observability, cost, and sustainability.
• Value & metrics: Establish VIPs/KPIs/OKRs (adoption, time‑to‑data, data trust, NPS, ROI); run quarterly value reviews, iterate the roadmap based on evidence.
• Data governance by design: Embed privacy, security, quality, and lifecycle controls (policies, lineage, access models, retention, auditability) into every increment, ensure GDPR compliance and data residency adherence.
• Data contracts & semantics: Maintain versioned schemas and contracts, define business rules and semantic layers that ensure interoperability across domains.
• Platform leverage & reusability: Reuse enterprise platforms, patterns, and reference architectures, drive reusability and scale across markets while meeting country‑specific requirements.
• Stakeholder & change leadership: Communicate clearly at all levels; manage dependencies and risks, prepare business cases, Investment Board inputs, release notes, and adoption communications.
• Incident, risk & release management: Triage issues, lead RCA, and prioritize preventative fixes, plan releases and change controls, coordinate rollbacks/hotfixes where needed.
• Enablement & adoption: Publish documentation, examples, and learning paths, champion catalog discoverability, access requests, and community channels.
• Financial stewardship: Own product budgets/forecasts, track benefits realization and ROI, report performance and outcomes to sponsors and Finance partners.
• Global alignment: Partner with global product, platform, and architecture teams to align roadmaps, share learnings, and represent EMEA needs and impact.

What you will need:

• Bachelor’s in Business, Computer Science, Engineering, or related field.
• 7–10+ years across product management/ownership, data platforms, analytics, or digital strategy. Medtech/pharma/consulting experience is a plus.
• Proven success delivering data products from concept to scaled adoption (data product mindset desirable).
• Strong grasp of data privacy (GDPR), regulatory frameworks, security, and AI ethics.
• Practical understanding of ELT/ETL, event streaming, data modeling, semantic layers, and production operations (SLAs/SLOs, observability).
• Expert backlog management, story writing, acceptance testing, and agile delivery at scale (Scrum/Kanban).
• Excellent communication and facilitation, able to influence executive, technical, and non‑technical audiences.
• Technical fluency and eagerness for continuous learning in Data & AI capabilities and products.

What do you offer:

• A passion for enabling teams with trustworthy, usable data, and a bias for measurable outcomes.
• Ownership mindset with high accountability for user satisfaction and product reliability.
• Pragmatic product instincts: you simplify, focus, and ship, balancing new value with platform hygiene and cost.
• Curiosity for emerging capabilities (semantic modeling, GenAI augmentation …etc.) and how to apply them responsibly.

What do we offer:

• A chance to shape the EMEA data product portfolio and set enterprise‑wide standards.
• A collaborative, global network and supportive coaching culture focused on your growth.
• Opportunities to lead high‑impact initiatives that advance analytics and AI adoption across diverse markets.
• A coaching culture environment focusing on your success and development!

Primary focus is providing administrative support for multiple managers and/or directors in selling organization in order to relieve them of administrative details. Works under general supervision and receives detailed instructions only for new assignments.

Your Responsibilities will include:

• Performs general administrative duties that may include coordinating meetings/calendar management, arranging travel, and ordering/maintaining supplies.
• Prepares expense reports for selling managers and directors.
• Schedules appointments and makes travel arrangements.
• Plans and coordinates meetings and events by coordinating calendars, scheduling catering, ordering audio-visual equipment and working with facilities to ensure room configurations.
• Assists in the preparation of reports, graphs, and presentations using Microsoft Office tools.
• Creates purchase orders in Ariba/MyBuy and manages a small number of invoices.
• Onboards new employees, maintains vacation records, and assist sales team with administrative tasks.
• Acts as an informed source of company policies and procedures by answering routine questions or routing to appropriate employees for answers.
• Conducts all aspects of the job with appropriate level of confidentiality and sensitivity to employee and organizational data by storing documents carefully and not disclosing confidential information except on a need-to-know basis.
• Willingness to be flexible, assume additional responsibilities, and coordinate activities with co-workers
• Ad hoc projects as required.

Required Qualifications

• 1 year of experience with Associate’s or Bachelor’s degree preferred.
• Proven experience working in a fast-paced organization.
• Strong communication skills (verbal and written) and interpersonal skills with ability to work across multiple levels of an organization.
• Strong proficiency in MS Outlook, SharePoint, Word, Excel & PowerPoint.
• Strong sense of responsibility and urgency as well as attention to detail.
• Strong customer-service orientation and professional demeanor.
• Highest ethical standards. Discretion and sound judgment when dealing with confidential and/or sensitive information.

Compensation fornon-exempt (hourly), non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation forexempt, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

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.

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-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