Latest Managed Services Jobs

Lead Analyst, Global Transparency Reporting - EMEA

This role involves leading and coordinating transparency reporting activities across EMEA markets to ensure compliance with regional and local regulations. The individual will work closely with compliance, legal, and finance stakeholders to validate and submit disclosures, while also driving process improvements through automation and data analytics. They will develop reporting insights, support audit readiness, and deliver training to strengthen organizational capability in transparency compliance.

Johnson & Johnson MedTech

On-site Permanent

Lead Analyst, Global Transparency Reporting - EMEA

This role involves leading and coordinating transparency reporting activities across EMEA markets to ensure compliance with regional and local regulations. The analyst will work closely with compliance, legal, and finance teams to validate, reconcile, and submit disclosures, while also driving process improvements through automation and digital solutions. The position emphasizes data analytics, regulatory intelligence, and stakeholder training to enhance reporting accuracy and operational efficiency.

Johnson & Johnson MedTech

Hybrid Permanent

Lead Analyst, Global Transparency Reporting - EMEA

Lead a regional team in managing transparency reporting across EMEA markets, ensuring compliance with evolving regulations and driving process improvements through data analytics and automation. This role involves coordinating disclosures, advising stakeholders, and enhancing digital reporting systems to maintain accuracy and efficiency. It combines compliance leadership with data-driven innovation in a global healthcare environment.

Johnson & Johnson MedTech

Hybrid Permanent

Lead Analyst, Global Transparency Reporting - EMEA

Lead Analyst responsible for coordinating transparency reporting across EMEA markets, ensuring compliance with regional and local regulations. The role involves stakeholder collaboration, regulatory monitoring, process improvement, and leveraging digital tools and automation to enhance reporting accuracy and efficiency. Focuses on data analytics, governance, and training to strengthen compliance operations.

Johnson & Johnson MedTech

Manager Regulatory Medical Writing X-TA

This role involves leading the preparation and finalization of clinical regulatory documents across multiple therapeutic areas, with a focus on strategic input, cross-functional collaboration, and compliance with global regulatory standards. The individual will lead writing teams, mentor junior staff, and drive process improvements within the medical writing function. Based in a hybrid work model, the position requires strong scientific communication skills and deep familiarity with ICH and other regulatory guidelines.

Johnson & Johnson MedTech Netherlands €68,600 – €119,600 pa

Hybrid Permanent

Manager Regulatory Medical Writing X-TA

This role involves leading the preparation and finalization of clinical and regulatory documents across multiple therapeutic areas, with a focus on strategic input, scientific accuracy, and compliance with regulatory standards. The manager will lead writing teams, mentor junior staff, and collaborate cross-functionally to ensure high-quality submissions. The position operates in a hybrid model, requiring onsite presence while supporting global regulatory initiatives.

Johnson & Johnson MedTech €60,400 – €103,960 pa

Hybrid Permanent

Manager Regulatory Medical Writing X-TA

Leads the preparation and finalization of clinical and regulatory documents across multiple therapeutic areas, providing scientific and strategic direction for writing teams. Manages timelines, mentors junior staff, and ensures compliance with regulatory standards such as ICH guidelines. Operates with high independence while collaborating closely with cross-functional teams to deliver high-quality medical content for submissions.

Johnson & Johnson MedTech €79,800 – €137,770 pa

Hybrid Permanent

Manager Regulatory Medical Writing X-TA

This role involves leading the preparation and finalization of clinical and regulatory documents within a global medical writing team, with a focus on cross-functional collaboration and scientific strategy. The individual will guide teams, ensure compliance with regulatory standards such as ICH, and mentor junior staff. Based in a hybrid work model, the position supports multiple therapeutic areas and drives process improvements in medical writing operations.

Johnson & Johnson MedTech €78,300 – €135,700 pa

Hybrid Permanent

Medical Writer II, X-TA

This role involves authoring and coordinating regulatory medical writing documents across key therapeutic areas such as Oncology, Immunology, and Neuroscience. The Medical Writer II will produce clinical study reports, protocols, and investigational brochures, ensuring compliance with ICH guidelines and internal standards. They will collaborate with cross-functional teams, contribute to document planning and review, and support quality control processes while adhering to regulatory and scientific best practices.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Medical Writer II, X-TA

A Medical Writer II in Regulatory Medical Writing will author and coordinate clinical and regulatory documents across therapeutic areas such as Oncology, Immunology, and Neuroscience. The role involves drafting protocols, clinical study reports, and regulatory submissions while collaborating with cross-functional teams. The position operates in a hybrid model with 3 days onsite weekly and requires strong scientific writing skills and familiarity with regulatory guidelines.

Johnson & Johnson MedTech Belgium €60,000 – €97,865 pa

Hybrid Permanent

Medical Writer II, X-TA

This role involves authoring and coordinating regulatory medical writing documents such as clinical study reports, protocols, and investigator brochures across key therapeutic areas including Oncology, Immunology, and Neuroscience. The Medical Writer II will work within a cross-functional team to ensure accurate, high-quality documentation in compliance with regulatory standards and internal guidelines, while also mentoring junior staff and contributing to process improvements. The position operates in a hybrid model with a mix of on-site and remote work.

Johnson & Johnson MedTech

Hybrid Permanent

Manager Regulatory Medical Writing XTA

Leads the preparation and finalization of clinical regulatory documents, providing scientific and strategic direction for medical writing teams. Provides mentorship, drives process improvements, and serves as a key liaison between cross-functional teams and regulatory stakeholders. Works independently on complex projects across multiple therapeutic areas.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Hybrid Permanent

Manager Medical Writing XTA

This role involves leading the preparation and finalization of clinical and regulatory documents across multiple therapeutic areas, with a focus on scientific strategy, project leadership, and cross-functional collaboration. The individual will act as a primary point of contact for medical writing activities, mentor junior staff, and ensure compliance with regulatory guidelines such as ICH. The position requires strong scientific communication, project management, and leadership skills within a hybrid work environment.

Johnson & Johnson MedTech United States US$117,000 – US$201,250 pa

Hybrid Permanent

Manager Medical Writing XTA

Leads the development and finalization of clinical and regulatory documents across multiple therapeutic areas, providing scientific and strategic direction for writing teams. Provides mentorship to junior staff, drives process improvements, and serves as a key liaison between medical writing and cross-functional teams. Works independently to ensure compliance with regulatory standards and supports submission activities.

Johnson & Johnson MedTech US$117,000 – US$201,250 pa

Hybrid Permanent

Manager Medical Writing XTA

Leads the preparation and finalization of clinical and regulatory documents within a cross-functional environment, providing scientific and strategic direction for medical writing activities across multiple therapeutic areas. Responsible for mentoring junior staff, driving process improvements, and ensuring compliance with regulatory standards such as ICH guidelines. Works closely with clinical teams to coordinate submissions and maintain high-quality documentation.

Johnson & Johnson MedTech US$117,000 – US$201,250 pa

Hybrid Permanent