Single Sponsor Clinical Project Manager II (Virology) - 1-2 days in Uxbridge (offices moving to[...]

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. 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 deliver – for one another, our customers, and, most importantly, for those in need.

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 building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.

Job Responsibilities:

• Plan, direct, create, and communicate clinical study timelines to ensure deliverables are produced on schedule.
• Gather input from cross-functional teams to create comprehensive plans for clinical studies.
• Ensure consistency of clinical study processes across clinical trials, adhering to standard operating procedures (SOP), good clinical practice (GCP), and specific country regulations.
• Oversee and resolve operational aspects of clinical trials in conjunction with project teams.
• Select sites and vendors, prepare clinical trial budgets, and ensure studies are conducted within clinical trial protocols.
• Monitor progress and follow up with team members and line managers when issues develop.
• Implement and prepare the clinical development strategy as outlined by the clinical teams.
• Develop trial recruitment strategies to ensure successful participant enrollment.

Qualifications:

• Bachelor's degree in a related field (e.g., Clinical Research, Life Sciences, Healthcare Management).
• Minimum of 5 years of experience in clinical project management or a related role.
• Proven track record of successfully managing clinical trials and ensuring adherence to SOP, GCP, and country regulations.
• Certification in Clinical Research (e.g., CCRP, CCRA) is preferred.
• Project Management Professional (PMP) certification is a plus.

Necessary Skills:

• Strong organizational and planning skills to create and manage clinical study timelines.
• Excellent communication skills to gather input from cross-functional teams and communicate plans effectively.
• Ability to oversee and resolve operational aspects of clinical trials.
• Knowledge of SOP, GCP, and country regulations to ensure consistency across clinical studies.
• Experience in site and vendor selection, budget preparation, and monitoring progress.
• Ability to implement and prepare clinical development strategies.
• Strong problem-solving skills to address issues that arise during clinical trials.

Roles within Clinical Project Management job family at the M23 level significantly impact the success of clinical trials by ensuring that all aspects of the study are conducted efficiently and effectively. Their oversight of operational aspects of clinical trials ensures consistency and adherence to SOP, GCP, and country regulations, which is crucial for the integrity and reliability of the study results.