Job Description

Company Description

Ergomed Group is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease.

Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia

Our company allows for employee visibility (you have a voice!) creative contribution and realistic career development.

We have nourished a true international culture here at Ergomed.

We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.

Come and join us in this exciting journey to make a positive impact in patient\xe2\x80\x99s lives.



The Executive Vice President, Global Operations will oversee CRO operations, including Clinical Operations, Project Management, Global Medical Affairs, Strategic Solutions and Patient Centricity, Biometrics, Study Start-Up and Regulatory Affairs. This role involves interaction with executive leadership, customers, business development, and project teams to coordinate clinical trials and services. It also includes providing strategic direction for global growth and consulting as needed. Additionally, the position involves offering scientific and therapeutic expertise, participating in defining corporate strategy, and ensuring staff\'s alignment with departmental and corporate objectives.

\xe2\x80\x8b\xe2\x80\x8bRole and Responsibilities\xe2\x80\x8b

Provides overall strategy and direction of clinical trials, processes and procedures globally.

Responsible for global budget, forecast and profitability.

Participates in customer proposals, Request for Information (RFIs), presentations, proposal defences and Steering Committees.

Provides scientific/regulatory oversight and project/therapeutic training to project teams.

Responsible for coordinating the acquisition of necessary medical/scientific input from outside experts/consultants/advisors.

Represents the Company by attending industry meetings, speaking engagements, participating in booth exhibitions, etc., and by publishing scientific or industry related articles in industry journals.

Participates in the development of Standard Operating Procedures (SOPs), medical/scientific tools, training, staffing requirements, etc.

Interacts with executive management and contributes scientific/medical input to other departments.

Ensures quality standards are set and maintained over all areas of responsibility.

Qualifications

• Degree educated (MSc or PhD preferred)
• Extensive global leadership experience in a CRO, ideally managing different functions
• Deep knowledge of drug development process and worldwide regulatory requirements
• Strategic and collaborative, with excellent communication skills

Additional Information

Why Ergomed

We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.

To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us.

We offer:

Training and career development opportunities internally

Strong emphasis on personal and professional growth

Friendly, supportive working environment

Opportunity to work with colleagues based all over the world, with English as the company language

Our core values are key to how we operate, and if you feel they resonate with you then Ergomed is a great company to join!

Quality

Integrity & Trust

Drive & Passion

Agility & Responsiveness

Belonging

Collaborative Partnerships

We look forward to welcoming your application.

Ergomed