Senior Regional Study Manager - REMOTE

Jobgether; Remote; GBP 60,000 - 75,000; Full time

Job summary

A clinical research organization is seeking a Senior Regional Study Manager in the UK. In this critical role, you will lead the delivery of clinical studies focused on Infectious Diseases and Vaccines. Responsibilities include budget management, developing monitoring plans, and training Clinical Research Associates. You should have at least 6 years of experience in Clinical Trial Management and a Bachelor's degree in a relevant field. This is a chance to join a dynamic team and impact clinical development positively.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement benefits

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifications

• Minimum of 6 years in Clinical Trial Management at a CRO or Pharmaceutical.
• 10+ years in clinical research required.
• Experience managing complex or global trials is advantageous.

Responsibilities

• Oversee clinical budgets for effective resource allocation.
• Develop monitoring plans and tools for study oversight.
• Train and mentor Clinical Research Associates.

Skills

Clinical Trial Management

Infectious Disease Studies

Vaccine Studies

Monitoring Experience

Team Leadership

Fluency in English

Education

Bachelor's degree in health or life sciences

Job description

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Senior Regional Study Manager. In this pivotal role, you will ensure the successful delivery of clinical studies focused on Infectious Diseases and Vaccines. Your substantial expertise will directly impact our clinical activities by managing budgets, developing monitoring plans, and driving enrollment. Additionally, you will liaise with various stakeholders, proactively identify risks, and provide essential reporting to ensure project objectives are met. Join our dynamic team to help shape the future of clinical development.

Accountabilities

• Oversee the clinical portion of the budget to ensure efficient resource allocation.
• Develop monitoring plans and tools for effective study oversight.
• Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
• Drive enrollment and lead study start-up activities, adhering to timelines.
• Review trip reports and implement corrective and preventative action plans as necessary.
• Foster productive relationships with Sponsors, vendors, and cross-functional teams.

Requirements

• A minimum of 6 years of experience in Clinical Trial Management at a CRO or Pharmaceutical Organization.
• Must have experience managing Infectious Disease and Vaccine studies.
• Bachelor's degree in health, life sciences, or relevant fields.
• At least 10+ years of relevant experience in clinical research.
• Preferred: 2+ years of monitoring experience.
• Experience in managing complex or global trials is advantageous.
• Preferred: Experience managing all trial components from start-up to database lock.
• Preferred: Experience in coaching/mentoring other CTMs and leading a team.
• Fluency in English (reading, writing, speaking).

Benefits

• Various annual leave entitlements.
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings for future savings.
• Global Employee Assistance Programme with 24-hour access to support.
• Life assurance.
• Flexible country-specific optional benefits, including childcare vouchers and discounted gym memberships.

Why Apply Through Jobgether?

We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

We appreciate your interest and wish you the best!

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