Senior Site Manager (H/F)

At Johnson & Johnson,we 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, andsolutions 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 jnj.com .

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.

Job Function:
R&D Operations

Job Sub Function:
Clinical Trial Support

Job Category:
Professional

All Job Posting Locations:
Issy-les-Moulineaux, France

Job Description:
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 driven Senior Site Manager, located in Paris region Ile-de France (France) to serve as the primary contact point between the Sponsor and the Investigational Site for trials in phases 2 to 4, located France (Hybrid).

Purpose:

The position is within the Oncology-hematology therapeutic area and will include monitoring 2-3 trials .

As 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.

Our new colleague should be flexible and is able to work independently.

We are seeking to hire a strong communicator, a quick learner, a problem solver, and a real team player.

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, Clinical Trial Manager (regional project manager) and Trial Delivery Leader.

You will be part of 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 French team that provides mutual support and opportunities to work together to identify new and improved ways of working.

You will be responsible for:


* Activities ranging from site feasibility and selection over site initiation and start-up, to preparation and conduct of ...