Single Sponsor Clinical Trial Manager - 2-3 days a week in Uxbridge

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.
• We are continuously building the company we all want to work for and our customers want to work with.

Job Responsibilities:

• Coordinate Phase III clinical research studies across Europe, ensuring all aspects of the study are meticulously planned and executed.
• Participate in and manage project meetings and conference calls with CROs, vendors, and multi-functional teams.
• Able to anticipate obstacles and proactively develop solutions to achieve project goals.
• Participate in abstract presentations, oral presentations and manuscript development activities.
• Interact and cooperate with individuals in other functional areas to address routine study issues.
• Assist in training for Clinical Trials Management Associates (CTMAs) and Clinical Project Assistants (CPAs).
• Assist in selecting CROs or Vendors.
• Coordinate CROs and Vendors.
• Responsible for updating study timelines.
• Ensure adherence to global and regional regulations and guidelines, staying up-to-date with any changes or updates.

Qualifications:

• Bachelor's degree in a related field (e.g., life sciences, clinical research).
• Regional Study Management experience in managing studies across European regions.
• In-depth knowledge of clinical research processes and regulations gained from a CRO or Pharma.
• CRO oversight experience.
• Strong project management and organizational skills.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Proficiency in using clinical trial management software and tools.

Necessary Skills:

• Strong analytical and problem-solving skills.
• Attention to detail and accuracy.
• Ability to manage multiple projects and priorities simultaneously.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
• Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.

Roles within the Clinical Trial Management job family at the P22 level are responsible for overseeing the development, coordination, and implementation of Phase I-IV clinical research studies at the organization's facilities. Individuals in these roles collaborate closely with the principal investigator, serve as liaisons between research subjects, client teams, investigators, and clinic operations teams, and meticulously plan logistics and resource usage.

These roles require tracking study progress in alignment with project milestones, client deliverables, and budget, while ensuring compliance with applicable regulations globally and by region.

Impact and Contribution:

Roles within the Clinical Trial Management job family at the P22 level significantly impact the success of clinical trials by ensuring that all aspects of the study are meticulously planned and executed. Individuals in these roles contribute to the design, implementation, and delivery of processes, programs, and policies, leveraging their in-depth knowledge and skills within the professional discipline.

By managing processes and potentially directing the work of lower-level professionals, these roles ensure that clinical trials are conducted efficiently and effectively, ultimately contributing to the advancement of medical research and the development of new treatments.

Core Focus:

• Overseeing the development and coordination of Phase I-IV clinical research studies.
• Collaborating with principal investigators and serving as liaisons between various stakeholders.
• Planning logistics and resource usage for clinical trials.
• Tracking study progress in alignment with project milestones, client deliverables, and budget.
• Ensuring compliance with global and regional regulations.
• Contributing to the design, implementation, and delivery of processes, programs, and policies.
• Managing processes and potentially directing the work of lower-level professionals.

Discover what our more than 29,000 employees already know: work here matters everywhere. We work hard, and smart, all in the name of getting much-needed therapies to those who need them most. A career with Syneos Health means your everyday work improves patients’ lives around the world.