Senior Site Manager (CRA)

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:
Remote (US), Somerville, New Jersey, United States of America

Job Description:

We are searching for the best talent for a Senior Site Manager (CRA) to support MedTech business.  Please note candidates must have access to an airport nearby due to the extensive travel requirements of the role.

This is a remote role available in multiple states within the United States.  While specific cities are listed in the Locations section for reference, please note they are examples only and do not limit your application.

We invite candidates from various locations to apply and encourage you to review the following states where this opportunity is available:

Eastern US Broadly:

Alabama, Arkansas, Connecticut, Delaware, Florida, Georgia, Illinois, Indiana, Iowa, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, New Hampshire, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Vermont, Virginia, West Virginia, Wisconsin

Purpose: The Senior Site Manager (Senior SM) serves as the primary contact point between the Sponsor and the Investigational Site.

The Senior SM is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), and applicable regulations and guidelines from study start-up through to site closure.

Responsibilities may include assisting with site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring, and close-out activities.

The Senior SM will partner with the Clinical Trial Leader (CTL) to ensure overall site management while performing trial related activities for assigned protocols.

The Senior SM may contribute to process improvement, training and mentoring of other Site Managers.

You will be responsible for:


* Act as primary local company contact for assigned sites for specific trials.


* May participate in site feasibility and/or pre-trial site assessment visits.


* Attend/participate in investigator meetings as needed.


* Execute activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by ...