Clinical Trial Manager

TN Spain; Cádiz; Presencial; GBP 50.000 - 60.000; Jornada completa

Descripción de la vacante

A leading company in clinical development is seeking a Clinical Trial Manager to oversee multiple clinical trials. The role requires operational expertise, project leadership, and a thorough understanding of clinical operations and regulatory compliance. Ideal candidates will have a Bachelor's degree and extensive experience in the field, with opportunities for remote working and flexible time off.

Servicios

Remote working options

Flexible time off

Paid holidays

Medical insurance

Tuition reimbursement

Retirement plans

Formación

• 5+ years of experience as a CRA in a CRO or pharmaceutical setting.
• Thorough knowledge of clinical operations and regulatory environment.
• Ability to mentor and train CRAs.

Responsabilidades

• Provide operational expertise and leadership to clinical trial teams.
• Ensure effective delivery of studies across all phases.
• Manage workload and priorities in a fast-paced environment.

Conocimientos

Communication

Leadership

Critical Thinking

Problem Solving

Educación

Bachelor’s Degree in health sciences

Herramientas

Microsoft Office

EDC

IVRS

CTMS

eTMF

Descripción del empleo

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Clinical Trial Manager (CTM) Role

The Clinical Trial Manager (CTM) provides operational expertise and leadership to multiple clinical trial teams, ensuring the effective and efficient delivery of all aspects of multiple studies across all phases of clinical study management. 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 applicable local regulations.

About Us

For more than 30 years, Veristat has been a global leader in clinical development.

• Supported over 760 Rare Disease Clinical Trials
• Supported over 160 Marketing Applications
• In 2022, supported 8 marketing applications that received regulatory approval

What We Offer

• The estimated salary range for this role is £50,000 - 60,000 plus applicable bonus. This range is specific to the UK and may vary by region based on local market data. Final salary depends on skills, experience, licensure, education, location, and market conditions.
• Benefits vary by location and may include remote working, flexible time off, paid holidays, medical insurance, tuition reimbursement, and retirement plans.

Qualifications and Skills

• Bachelor’s Degree required; degrees in health sciences preferred.
• 5+ years of experience as a CRA in a CRO or pharmaceutical setting, with demonstrated project leadership skills.
• Thorough knowledge of clinical operations, development processes, ICH / GCP, and regulatory environment.
• Ability to mentor, coach, and train CRAs.
• Excellent communication skills in English; proficiency in additional languages is a plus.
• Knowledge of therapeutic areas relevant to the study for appropriate input on study documents.
• Proficiency in Microsoft Office and ability to learn new clinical systems (EDC, IVRS, CTMS, eTMF, etc.).
• Self-motivated, team-oriented, and able to work independently.
• Strong critical thinking and problem-solving skills.
• Ability to manage workload and priorities in a fast-paced environment.

Travel requirements : Up to 30%, including UK, Europe, and international travel. Valid Driver’s License required.

Automated Decision Making : All applicants are reviewed manually by the Veristat Talent Acquisition team; no automated decision-making process is used.

LI-RD1

Veristat is an equal opportunity employer, committed to diversity and inclusion for all employees.

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