Senior Clinical Trial Assistant

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, 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 humanity. Learn more at https://www.jnj.com

Job Function:
R&D Operations

Job Sub Function:
Clinical Trial Project Management

Job Category:
Professional

All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom

Job Description:

Senior Clinical Trial Assistant

About Innovative Medicine

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 https://www.jnj.com/innovative-medicine 

We are searching for the best talent for a Senior, Clinical Trial Assistant (Senior CTA) located High Wycombe, United Kingdom (Hybrid: 3 days per week onsite) to support the Local Trial Manager (LTM) and/or Site Manager (SM) to ensure optimal management of all documents with logistical and administrative tasks related to trial start-up, execution and closing of clinical trials.

The Senior CTA ensures trial related activities are compliant with GCO SOPs, policies and local regulatory requirements and contributes to process improvement, training and mentoring of other CTAs.

The Senior, CTA contributes to central business supports and process optimization with the support of other relevant functions in line with company’s requirements and business needs.

Partners with Business Operations, CTA team, study teams and key stakeholders (e.g.

Finance, Procurement etc.) to support routine clinical operations activities.

Are you ready to join our team? Then please read further!

Principal Responsibilities:



* Provide administrative and logistical support to LTM and/or SM in tracking progress of the trial, management of study data, budget, organizing meetings, mailing and correspondence, materials, drug distribution and other relevant tasks as appropriate in adherence to relevant SOPs, policies and local regulatory requirements.


* Supports the local study team in performing site feasibility and/or country feasibility.


* Maintains information in relevant systems.


* Ensures current versions of the required trial documents, trial-related materials and supplies are provided to the investigational site within required timeframes, as applicable.


* Support LTM and/or SM in collecting/preparing documents required for study startup/submissi...