Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

As a Clinical Trial Assistant, you will support the operational management of international clinical studies and work closely with Clinical Project Managers and CRA teams across multiple countries. You will play a key role in study coordination, documentation management, regulatory support, and clinical operations activities.

Key Responsibilities

Internal Opportunity | 2nd Officer | Skandi Skansen

Application Deadline: 25.10.26

DOF is pleased to announce an internal career opportunity as we continue to deliver safe and efficient offshore operations.

We are looking for a new team member to join the vessel from 11.11.2026. A handover period prior to embarkation may be required.

Rotation: 5 weeks

Operational Area: Worldwide

In this role, you will contribute to the safe and efficient execution of daily operations while helping maintain DOF's high operational standards. Working closely with colleagues on board, you will play an important part in supporting operational performance and a strong safety culture.

This opportunity is ideal for internal candidates looking to broaden their experience, take on new responsibilities, and further develop their careers within DOF. We are committed to providing a working environment that promotes collaboration, professional development, and continuous learning.

Who We Are

DOF is a leading provider of integrated marine and subsea services to the global offshore energy market. We combine expertise, assets, and technology to execute integrated subsea and offshore operations safely and reliably, every time.

Internal Opportunity | 2nd Officer | Skandi Skansen

Application Deadline: 29.10.26

DOF is pleased to announce an internal career opportunity as we continue to deliver safe and efficient offshore operations.

We are looking for a new team member to join the vessel from 09.12.2026. A handover period prior to embarkation may be required.

Rotation: 5 weeks

Operational Area: Worldwide

In this role, you will contribute to the safe and efficient execution of daily operations while helping maintain DOF's high operational standards. Working closely with colleagues on board, you will play an important part in supporting operational performance and a strong safety culture.

This opportunity is ideal for internal candidates looking to broaden their experience, take on new responsibilities, and further develop their careers within DOF. We are committed to providing a working environment that promotes collaboration, professional development, and continuous learning.

Who We Are

DOF is a leading provider of integrated marine and subsea services to the global offshore energy market. We combine expertise, assets, and technology to execute integrated subsea and offshore operations safely and reliably, every time.

Join our team as a Crane Technician!

DOF is seeking skilled and knowledgeable Crane Technician with experience working on Subsea projects or within the Offshore Oil & Gas Industry.

DOF operates Subsea, Anchor Handling Tug Supply and Platform Supply Vessels within the Oil and Gas Industry and requires a Crane Technician with experience in the industry and on these vessel types. These positions will ensure the safe and efficient operations on DOF Vessels by maintaining the crane and lifting gear as appointed by the Chief Engineer or his/her substitute.

Crane Technicians that work with DOF take pride in our assets and work to the highest standards to deliver safe and efficient operations to our clients. Our team aligns to DOF's values; Respect - Integrity - Teamwork - Excellence - And above all we are Safe.

This is an opportunity to express interest in joining our team and utilising your skills on our world class fleet of vessels.

Requirements

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

The successful candidate will play a key role in driving innovation, optimizing pharmacovigilance processes and improving data governance following the implementation of a new safety database platform. This position requires a strong combination of pharmacovigilance subject matter expertise, project leadership and a consulting mindset, with the ability to bridge business operations, digital technology teams and external solution providers.

Key Responsibilities

ETO Skandi Vega

Application Deadline: 01.11.2026

DOF is pleased to announce an internal career opportunity as we continue to deliver safe and efficient offshore operations.

We are looking for a new team member to join the vessel from 03.02.2027. A handover period prior to embarkation may be required.

Rotation: 4 weeks
Operational Area: North Sea

In this role, you will contribute to the safe and efficient execution of daily operations while helping maintain DOF's high operational standards. Working closely with colleagues on board, you will play an important part in supporting operational performance and a strong safety culture.

This opportunity is ideal for internal candidates looking to broaden their experience, take on new responsibilities, and further develop their careers within DOF. We are committed to providing a working environment that promotes collaboration, professional development, and continuous learning.

Who We Are

DOF is a leading provider of integrated marine and subsea services to the global offshore energy market. We combine expertise, assets, and technology to execute integrated subsea and offshore operations safely and reliably, every time.

3rd engineer Skandi Mongstad

Application Deadline: 22.10.26

DOF is pleased to announce a career opportunity as we continue to deliver safe and efficient offshore operations.

We are looking for a new team member to join the vessel from 08.12.26. A handover period prior to embarkation may be required.

Rotation: 4 weeks
Operational Area: North Sea

In this role, you will contribute to the safe and efficient execution of daily operations while helping maintain DOF's high operational standards. Working closely with colleagues on board, you will play an important part in supporting operational performance and a strong safety culture.

This opportunity is ideal for candidates looking to broaden their experience, take on new responsibilities, and further develop their careers within DOF. We are committed to providing a working environment that promotes collaboration, professional development, and continuous learning.

Who We Are

DOF is a leading provider of integrated marine and subsea services to the global offshore energy market. We combine expertise, assets, and technology to execute integrated subsea and offshore operations safely and reliably, every time.

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

We are looking for an experienced Medical Affairs Consultant / Therapeutic Area Medical Lead to provide medical leadership. The role focuses on ensuring the continuity of Medical Affairs activities, driving the execution of regional medical strategies and plans and fostering effective collaboration with regional and local medical teams to support ongoing projects and business objectives.

Key Responsibilities

• Lead and execute Medical Affairs activities within dermatology and/or rheumatology.
• Support regional medical strategies and operational medical plans across European markets.
• Collaborate with Medical Heads, Medical Advisors and cross-functional stakeholders.
• Coordinate scientific activities, including advisory boards, congresses and medical education initiatives.
• Support evidence generation projects, including Real-World Evidence (RWE) and Non-Interventional Studies (NIS).
• Engage with external medical experts and key opinion leaders (KOLs).
• Ensure scientific accuracy, regulatory compliance and alignment with medical governance.
• Provide operational continuity during temporary staffing gaps.

At SeaLink, we believe in connection and teamwork. People come and stay at SeaLink – because of “one boat, one team” we might have all arrived on different ships, but we are all on the same boat together, working towards a common goal.

About the role:

Reporting to Group Financial Controller, the Accounts Payable Officer plays a key role in ensuring supplier invoices are processed accurately, approved appropriately, and paid on time. This position supports operations across our passenger, freight, logistics and commuter services, helping maintain strong financial controls, positive supplier relationships and accurate financial records.

We're looking for an organised and detail-focused Accounts Payable professional who enjoys working in a fast-paced environment. You'll have a strong eye for accuracy, excellent communication skills, and a proactive approach to managing supplier queries, reconciliations and payment processes.

This is a part-time position working 25 hours per week (5 hours per day, Monday to Friday) and is based on-site in the Auckland CBD.

Key accountabilities include:

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

We are looking for a Senior Clinical Project Manager to support the operational management of an international clinical trial in pediatric oncology. This role offers the opportunity to work in a highly collaborative environment and contribute to innovative research programs with global impact.

Key Responsibilities

• Lead and coordinate the operational conduct of international clinical studies.
• Oversee study timelines, milestones, budget, and quality objectives.
• Manage relationships with investigational sites, CROs, vendors, and study stakeholders.
• Ensure compliance with ICH-GCP, regulatory requirements, and study procedures.
• Monitor study progress, patient recruitment, and site performance.
• Identify risks and implement mitigation plans to ensure successful study delivery.
• Coordinate cross-functional teams and facilitate project governance meetings.
• Contribute to study reporting, inspection readiness, and continuous process improvement.

Requirements