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*Description*

At Nuvance Health, we enjoy the benefits of a two-state system as we cultivate an inclusive culture where everyone feels welcomed, respected and supported. Together, we are a team of 15,000+ strong hearts and open minds. If you share our values of connected, personal, agile and imaginative, we invite you to discover what’s possible for you and your career.

Danbury Hospital, a 456-bed acute care hospital, has been providing award-winning, personalized patient care to the people of Western Connecticut for 140 years. Our specialty areas of excellence include a Level III NICU, a certified Thrombectomy-Capable Stroke Center, and compassionate psychiatric care, including a partial-hospitalization program.

Our accolades include the following:

* The Leapfrog Group - Grade A for quality and patient safety

* U.S. News & World Report - High performance in heart failure treatment

* Healthgrades - One of America’s 50 Best Hospitals

* Surgical Review Corporation (SRC) - Robotic Center of Excellence

* Joint Commission - Gold seal of approval in spine surgery

At Danbury Hospital, we take great pride in our team members and their passion for providing the best care possible—always with heart. For many of our team members, that care extends beyond the walls of our hospital. We volunteer at local non-profits and participate in community initiatives and events. Our dedication to the health and well-being of our entire community makes this a truly special place to work.

*Summary:*

The Project Manager for Vascular Research plans, directs, coordinates, and delivers activities for designated clinical study projects to ensure that project objectives of quality, scope, cost, and time are accomplished.

*Responsibilities:*

* Leads and manages clinical research projects from initiation through completion.

* Serves as the subject matter expert for assigned protocols, guiding cross-functional study teams.

* Coordinates with regulatory bodies (e.g. FDA) for submissions, revisions and required reporting.

* Monitors study enrollment, retention, and performance metrics; address deviations proactively.

* Develops and implements strategies to support recruitment and retention efforts.

* Identifies operational risks and collaborates on mitigation strategies with study teams.

* Oversees development and execution of Corrective and Preventive Action (CAPA) and studies specific oversight plans.

* Maintains Trial Master File (TMF) and ensures inspection readiness.

* Supports internal and external audits in collaboration with Quality Assurance.

* Manages study budgets and timelines; reviews and approves related invoices and timesheets.

* Leads team meetings and coordinates study specific training with the Director of Surgical Research.

* Escalates issues with clear documentation of task ownership, resolution timelines, and project impact.

* Maintains and Models Nuvance Health Values.

* Demonstrates regular, reliable, and predictable attendance.

* Performs other duties as required.

*Education, Skills and Experience:*

* BS. required– preferably in a life science field or equivalent (includes RN degree); MS or PhD preferred.

* Healthcare professional with at least 4 years of clinical experience, or Science Graduate with at least 4 years’ experience in clinical research, with a track record in successfully managing clinical trial sites.

* Prior project management experience required.

* High level of proficiency with Excel and MS Office; ability to master various electronic platforms for data entry and clinical trial management.

* Experience with vascular clinical trials and/or cancer therapies is highly preferred (required for senior level project managers).

* Strong verbal and written communication skills in English required.

* Well-developed critical thinking and analytical skills, with the ability to anticipate problems relating to projects and to develop and implement solutions.

* Able to seek out multiple and diverse perspectives; open to continuously refining your approach based on feedback and new information.

* Knowledgeable of the initiation, conduct, and completion of clinical trials, study endpoints, and clinical databases.

* Well-developed and effective written and verbal communication skills, including report writing, preparing, and delivering presentations, and various correspondence and meeting platforms.

Salary Range: $45.93 - $85.29 Hourly, commensurate with experience.

With strong hearts and open minds, we’re pushing past boundaries and challenging the expected, all in the name of possibility. We are neighbors caring for neighbors, working together as partners in health to improve the lives of the people we serve. If you share our passion for the health of our communities, advance your career with Nuvance Health!

We are an equal opportunity employer

Qualified applicants are considered for positions and are evaluated without regard to mental or physical disability, race, color, religion, gender, national origin, age, genetic information, military or veteran status, sexual orientation, marital status or any other classification protected under applicable Federal, State or Local law.

We will endeavor to make a reasonable accommodation to the known physical or mental limitations of a qualified applicant with a disability unless the accommodation would impose an undue hardship on the operation or our business. If you believe you require such assistance to complete this form or to participate in an interview, please contact Human Resources at 203-739-7330 (for reasonable accommodation requests only). Please provide all information requested to ensure that you are considered for current or future opportunities.