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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 Support
Job Category: Professional
All Job Posting Locations: High Wycombe, Buckinghamshire, United Kingdom
Job Description: Associate Site Manager
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 a driven Associate Site Manager to serve as the primary contact point between J&J Innovative Medicine and the Investigational Site for trials in phases 2-4. The head office location is in High Wycombe, Buckinghamshire, UK, and this position is home-based. The role involves monitoring trials within the Immunology therapeutic area, ensuring compliance with protocols, SOPs, GCP, and regulations, and collaborating with various trial team members. The candidate should be flexible, independent, a quick learner, and a good communicator, capable of working remotely and as part of a team.
The responsibilities include:
1. Activities from site feasibility and selection, to site initiation, start-up, monitoring, and close-out.
2. Implementing a risk-based monitoring model and working with sites to resolve issues.
3. Ensuring accurate and complete trial data, managing data entry, and query resolution.
4. Contributing to recruitment and retention strategies.
5. Documenting trial activities and communicating progress and issues.
6. Becoming a local expert on assigned protocols and therapeutic areas.
7. Participating in process improvement and training.
Qualifications include:
* A BA or BS in Life Sciences, Nursing, or related field (or equivalent experience).
* At least 2 years of clinical trial monitoring experience preferred.
* Knowledge of therapeutic areas, GCP, laws, and regulations.
* Strong IT skills and ability to operate various systems.
* Ability to work independently and as part of a team.
* Excellent communication and influencing skills.
* Willingness to travel up to 50%.
* Proficiency in English, both written and oral.
We offer a competitive salary, extensive benefits, flexible working, and career development opportunities. Johnson & Johnson is an equal opportunity employer committed to diversity and inclusion. Reasonable accommodations are available for individuals with disabilities; please contact us to request assistance.
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