Single Sponsor Sr Clinical Trial Manager (Global Site Management) UK based - fully home based

Syneos Health; United States; Remote; USD 90,000 - 130,000; Full time

Job summary

Syneos Health is searching for a Single Sponsor Sr Clinical Trial Manager to lead global site management for Oncology studies. The ideal candidate will have expertise in site management, strong leadership skills, and experience in an international clinical trial environment. This fully home-based role requires strategic oversight of Phase 1 studies, ensuring compliance and operational success while collaborating with various stakeholders.

Benefits

Career development and progression

Total rewards program

Supportive and engaged line management

Qualifications

• Ability to lead and align teams to achieve project milestones.
• Experience working in an international environment.
• Understanding of clinical trial management financial principles.

Responsibilities

• Provide direction and operational expertise for Clinical Site Management activities.
• Collaborate with key stakeholders in Oncology studies.
• Represent CSM globally as part of Clinical Study Team.

Skills

Leadership

Site Management

Problem Solving

Conflict Resolution

Critical Thinking

Education

Bachelor’s degree or RN in a related field

Tools

Good Computer Skills

Job description

Description

Single Sponsor Sr Clinical Trial Manager (Global Site Management) UK based - fully home based

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies because we are passionate to change lives.

Discover what our 29,000 employees across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

• We are passionate about developing our people through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition; and total rewards program.
• We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture unites us globally, and we are dedicated to taking care of our people.
• We are continuously building the company we all want to work for and our customers want to work with. Bringing together diversity of thoughts, backgrounds, cultures, and perspectives creates a place where everyone feels like they belong.

Job Responsibilities

This Global Sr CTM role provides direction and operational expertise for all Clinical Site Management (CSM) activities in assigned studies. The position can be assigned as the global study strategy leader or as an area site execution leader, depending on the study size, complexity, and geographic scope. The role involves working within a strong portfolio of Oncology studies and influencing key stakeholders. If assigned as the global site management leader, the individual is a key member of the Clinical Study Team representing CSM globally.

Qualifications

• Bachelor’s degree or RN in a related field or equivalent experience
• Ability to lead and align teams to achieve project milestones
• Experience working in an international environment
• Expertise in site management and monitoring (clinical or central)
• Preferred experience with risk-based monitoring
• Understanding of clinical trial management financial principles and budgeting
• Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements
• Good computer skills
• Strong conflict resolution skills
• Problem-solving skills and a risk management approach
• Critical thinking skills
• Oncology experience is beneficial. Moderate travel (~20%) may be required.

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products, and conducted over 200 studies across 73,000 sites and 675,000+ trial patients.

No matter your role, you’ll take the initiative and challenge the status quo in a highly competitive environment. Learn more at Syneos Health.

Additional Information

Tasks, duties, and responsibilities are not exhaustive. The company may assign other tasks at its discretion. Equivalent experience, skills, and education will be considered. This description does not create a contract. The company is committed to compliance with applicable laws and regulations, including the EU Equality Directive and the Americans with Disabilities Act.

Summary

Roles at the M24 level in Clinical Trial Management oversee Phase 1 studies, collaborating with investigators, research subjects, and operational teams. They plan logistics, track progress, ensure compliance, and manage teams, contributing significantly to the organization’s research outcomes. Their strategic and tactical leadership ensures operational success aligned with organizational goals.

Core Focus

• Overseeing Phase 1 clinical research development and implementation
• Collaborating with investigators, research subjects, and operational teams
• Planning logistics and resource usage
• Tracking study progress and ensuring regulatory compliance
• Managing teams and delivering operational results
• Providing strategic direction across the organization