Clinical Trial Manager

Veristat; Albacete; A distancia; EUR 50.000 - 60.000; Jornada completa

Descripción de la vacante

A leading company in clinical development seeks a Clinical Trial Manager to oversee multiple clinical trial teams. The role involves ensuring compliance and quality throughout the study lifecycle. Candidates should have a Bachelor’s degree in health sciences and significant experience in clinical operations. Benefits include remote work and comprehensive health coverage.

Servicios

Remote work

Flexible time off

Medical insurance

Tuition reimbursement

Retirement plans

Formación

• At least 5 years' experience as a CRA in CRO or pharmaceutical settings.
• Strong knowledge of ICH / GCP and regulations.

Responsabilidades

• Overseeing study management to ensure compliance and quality.
• Providing operational expertise and leadership to clinical trial teams.

Conocimientos

Leadership

Communication

Knowledge of clinical operations

Educación

Bachelor’s Degree in health sciences

Herramientas

Microsoft Office

EDC

IVRS

CTMS

eTMF

Descripción del empleo

Join to apply for the Clinical Trial Manager role at Veristat .

The Clinical Trial Manager (CTM) provides operational expertise and leadership to multiple clinical trial teams to ensure the effective and efficient delivery of all aspects of clinical studies across all phases. This is done in accordance with Veristat Policies, Standard Operating Procedures (SOPs), conventions, instructions, and current Good Clinical Practice (GCP), International Conference on Harmonization (ICH), and local regulations.

Job Description

The CTM supports multiple clinical trial teams, overseeing study management to ensure compliance and quality throughout the study lifecycle.

What We Do

For over 30 years, Veristat has been a global leader in clinical development, supporting over 760 rare disease clinical trials and 160+ marketing applications, with 8 approvals in 2022. Learn more about our core values!

What We Offer

• Estimated salary range : £50,000 - 60,000 plus bonus, varies by region and experience.
• Benefits include remote work, flexible time off, holidays, medical insurance, tuition reimbursement, and retirement plans.

What We Look For

• Bachelor’s Degree, preferably in health sciences.
• At least 5 years' experience as a CRA in CRO or pharmaceutical settings, with project leadership skills.
• Strong knowledge of clinical operations, development processes, ICH / GCP, and regulations.
• Mentoring, coaching, and training abilities for CRAs.
• Excellent communication skills in English; additional languages a plus.
• Knowledge of therapeutic areas and clinical systems (EDC, IVRS, CTMS, eTMF).
• Proficiency in Microsoft Office and ability to learn new clinical software.
• Self-motivated, team player, capable of managing workload and priorities.

Travel up to 30% required; valid driver’s license necessary.

Veristat is an equal opportunity employer committed to diversity and inclusion.

• Seniority level : Mid-Senior level
• Employment type : Full-time
• Job function : Research, Analysis, IT
• Industry : Research Services

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