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Senior Analytical Monitor

The Senior Analytical Monitor role involves conducting analytical monitoring activities for multiple clinical trials, ensuring compliance with regulations and company policies. Responsibilities include performing regular reviews, detecting issues early, and collaborating with Site Managers and Central Monitoring Managers to improve data reliability and site satisfaction.

Johnson & Johnson MedTech High Wycombe, United Kingdom
Hybrid Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include coordinating data-driven risk oversight, maintaining clinical quality plans, and facilitating regular risk updates to R&D colleagues.

Johnson & Johnson MedTech High Wycombe, United Kingdom
On-site Permanent
Smith & Nephew logo

Senior Orthopaedic Sales Specialist

This role involves working as a trusted expert in orthopaedic revision surgery, supporting complex procedures in operating theatres, and driving the adoption of innovative technologies, including robotics. You will develop account plans, collaborate with sales teams, and gather market intelligence to strengthen Smith & Nephew's market position.

Smith & Nephew Cambridge, United Kingdom
Hybrid Permanent
Smith & Nephew logo

Senior Orthopaedic Sales Specialist

This role involves working closely with surgeons and key accounts to drive the adoption of advanced orthopaedic revision technologies, including robotics. You will lead sales strategies, support complex procedures, and gather market intelligence to strengthen Smith & Nephew's position in the M1 Corridor to the East of England.

Smith & Nephew Chatham, ME4 4NP, United Kingdom
Hybrid Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Responsibilities include active participation in study activities, regular risk reviews, maintaining clinical quality plans, and communicating risk updates to stakeholders.

Johnson & Johnson MedTech United States
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. They actively participate in risk management activities, maintain clinical quality plans, and communicate risk updates to stakeholders through regular reviews and governance meetings.

Johnson & Johnson MedTech
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include active participation in study activities, regular risk reviews, maintaining clinical quality plans, and facilitating risk updates to R&D colleagues.

Johnson & Johnson MedTech
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Responsibilities include active participation in study activities, maintaining clinical quality plans, and facilitating regular risk reviews and updates.

Johnson & Johnson MedTech
On-site Permanent

Senior Specialist, Clinical Risk Management

The Senior Specialist, Clinical Risk Management, collaborates with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include participating in risk assessments, maintaining clinical quality plans, and communicating risk updates to R&D colleagues through regular review cycles.

Johnson & Johnson MedTech Belgium
On-site Permanent

Specialist, Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. They actively participate in study activities, maintain clinical quality plans, and communicate risk updates to R&D colleagues through regular review cycles.

Johnson & Johnson MedTech High Wycombe, United Kingdom
On-site Permanent

VELYS Trauma Marketing Manager

The VELYS Trauma Marketing Manager will lead the launch and establishment of the new VELYS Trauma system within the DPS International business and Trauma Platforms. Key responsibilities include developing and executing international strategies, partnering with cross-functional teams, and ensuring market access and clinical evidence strategies are in place.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. They actively participate in risk management activities, maintain clinical quality plans, and communicate risk updates to stakeholders through regular review cycles.

Johnson & Johnson MedTech United States
On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include active participation in study activities, maintaining clinical quality plans, and facilitating regular risk reviews and updates.

Johnson & Johnson MedTech
On-site Permanent

Specialist Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include coordinating data-driven risk oversight, maintaining clinical quality plans, and communicating risk updates to stakeholders through regular review cycles.

Johnson & Johnson MedTech
On-site Permanent

Specialist, Clinical Risk Management Oncology

The Specialist, Clinical Risk Management Oncology, works closely with trial teams to identify, assess, and mitigate quality risks that could impact trial data integrity, patient safety, and regulatory compliance. Key responsibilities include coordinating data-driven risk oversight, maintaining clinical quality plans, and communicating risk updates to R&D colleagues through regular review cycles.

Johnson & Johnson MedTech Belgium
On-site Permanent

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