Senior Global Clinical Lead – Trials & Team Leadership

Novotech; Wien; On-site; EUR 120,000 - 151,000; Full time

Job summary

Novotech is seeking a Clinical Lead (CL) and Senior Clinical Lead to guide multi-country clinical teams, coordinate site management and monitoring activities, and deliver on-time clinical milestones. You will develop the clinical monitoring plan, recruitment strategy, training, and ensure high-quality data.

Responsibilities include site identification, CMP/MVR development, training, CTMS metrics, risk management, and collaboration with PM/RSM across regions.

Qualifications

• Solid communication skills with fluency in English (verbal and written).
• Experience in coaching and mentoring clinical teams.
• Strong understanding of risk management principles in multi-country trials.
• Ability to manage large multi-centre clinical trials at regional/global levels.
• Knowledge of ICH-GCP and applicable policies; ability to navigate regulatory landscapes.

Responsibilities

• Manages day-to-day clinical project team ensuring deliverables and mentoring as needed.
• Lead site identification and site selection activities.
• Prepare and attend KOM and present at investigator meetings.
• Drive CMP and MVR development; ensure CRA understanding and adherence to timelines.
• Coordinate regulatory start-up activities across regions; manage IP and non-IP supplies across regions.
• Develop subject recruitment strategies and monitor study materials before SIV.
• Ensure timely MVR reviews and trend reporting; maintain compliance with CMP.

Skills

English fluency

Leadership

Project coordination

Risk management

Communication

Clinical trial management

Education

Graduate in a clinical or life-science related field

Master's degree or higher level preferred

Tools

Veeva

CTMS

Job description

Novotech is seeking a Clinical Lead (CL) and Senior Clinical Lead to guide multi-country clinical teams, coordinate site management and monitoring activities, and deliver on-time clinical milestones. You will develop the clinical monitoring plan, recruitment strategy, training, and ensure high-quality data.

Responsibilities include site identification, CMP/MVR development, training, CTMS metrics, risk management, and collaboration with PM/RSM across regions.