Clinical Trial Manager - Virology

Hobson Prior International Ltd; Uxbridge; Hybrid; GBP 40,000 - 60,000; Part time

Job summary

A biotechnology organization is seeking a Clinical Trial Manager - Virology to oversee clinical trials in the EMEA region. This role involves managing study timelines, collaborating with global teams, and ensuring compliance with regulations. Candidates should have a scientific background and experience in clinical studies. The position requires a mix of onsite presence and remote work.

Qualifications

• Experience in managing or coordinating clinical studies.
• Knowledge of FDA, EU regulations, ICH guidelines, and GCP standards.
• Monitoring or co-monitoring experience is desirable.

Responsibilities

• Manage regional aspects of clinical trials, ensuring timelines and budgets are met.
• Draft and review key study documents such as protocols and consent forms.
• Collaborate with vendors and CROs to execute studies effectively.
• Monitor study progress and address any issues that arise.

Skills

Strong organizational skills

Communication skills

Problem-solving skills

Ability to prioritize tasks

Education

Background in a scientific discipline or nursing qualification

Job description

Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science.

Hobson Prior is seeking a Clinical Trial Manager - Virology to join a biotechnology organization on a contract basis. In this role, you will oversee regional management of clinical trials (Phase Ib-III) with a focus on the EMEA region. You will work closely with global teams and external partners to ensure the successful execution of studies from start-up to close-out. This position requires a mix of onsite presence (3-5 days per week) and remote work.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Manage regional aspects of clinical trials, ensuring timelines and budgets are met.
• Draft and review key study documents such as protocols, consent forms, and reports.
• Collaborate with vendors and CROs to execute studies effectively.
• Monitor study progress and address any issues that arise.
• Train investigators, coordinators, and vendors on study requirements.
• Oversee site budget and contract processes.
• Support data review and preparation of study reports.
• Contribute to study logistics, planning, and stakeholder management.
• Provide expertise on country-specific regulations and site suitability.
• Participate in cross-functional team activities and initiatives.

Key Skills and Requirements:

• Background in a scientific discipline or nursing qualification.
• Experience in managing or coordinating clinical studies.
• Familiarity with virology is beneficial but not essential.
• Knowledge of FDA, EU regulations, ICH guidelines, and GCP standards.
• Strong organizational, communication, and problem-solving skills.
• Ability to prioritize tasks and adapt to changing environments.
• Monitoring or co-monitoring experience is desirable.
• Willingness to travel internationally as needed.

For more information, please contact Athi Singata.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

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