Senior Site Manager; Senior Clinical Research Assistant

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and cured where treatments are smarter and less invasive and solutions are our expertise in Innovative Medicine and Med Tech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at .

As guided by Our Credo Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson we respect the diversity and dignity of our employees and recognize their merit.

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Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way. Learn more at are searching for the best talent for a Senior Site Manager to serve as the primary contact point between the Sponsor and the Investigational Site for Oncology trials in phases 2 to 4.

In other organisations the Site Manager may be known as Clinical Research Associate or Monitor. The head office location is in High Wycombe Buckinghamshire and this position is home-based.

As a Senior Site Manager you will be responsible for maintaining ongoing inspection readiness and compliance with the clinical trial protocol Standard Operating Procedures (SOP) Good Clinical Practice (GCP) and applicable regulations from study start-up through to site closure. You should be flexible and be able to work independently. We are seeking to hire a strong communicator a quick learner a problem solver and a real teammate.

You will be responsible for oversight of clinical trial protocols at a site level and will collaborate closely with a Local Trial Manager (country project manager) Clinical Trial Assistant and Clinical Trial Manager (regional project manager).

You will work in a hardworking enthusiastic and committed study team eager to deliver and help improve the lives of millions of patients. You will also be part of a wider local UK team that provides mutual support and opportunities to work together to identify new and improved ways of working.

• Activities ranging from site feasibility and selection over site initiation and start-up to preparation and conduct of site monitoring oversight of key performance indicators and site/study close-out in complex clinical trials.
• The implementation of a site-level analytical risk-based monitoring model and for working with the site to ensure timely resolution of issues and deviations identified during monitoring visits.
• Ensuring accuracy and completeness of all trial data including safety data. Managing timely data entry and query resolution in collaboration with site staff.
• Co-creating site-level recruitment and retention strategies and implementation of mitigation actions in partnership with other functional areas.
• Ensuring full documentation of trial related activities in all study files; communicates site and study progress and issues to the Local Trials manager and central study teams.
• Being the local expert in assigned protocols and build the necessary therapeutic area knowledge.
• Coaching or mentoring less experienced colleagues.
• May participate to process improvement and training. Leading and/or participating in special initiatives as assigned. May assume additional responsibilities or special initiatives such as Champion or Subject Matter Expert.

• BA/BS degree in Life Sciences Nursing or related scientific field (or equivalent experience)
• A minimum of 3 years of clinical trial monitoring experience is preferred however other relevant working experiences and skills may be considered by the hiring manager
• Knowledge of Oncology therapeutic area is an asset
• Strong proven understanding of GCP local laws and regulations
• Strong IT skills and ability to operate and use various systems and databases
• Ability to establish a home office
• Strong team member and self-starter with the ability to work independently
• Strong communication and influencing skills to effectively manage study sites both remotely and face-to-face.
• Willingness to travel up to 50% (up to 2-3 days per week) with some overnight stays as necessary

We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority we have a flexible working environment as we value work-life balance. We offer career…