Senior Clinical Trial Manager - Cardiovascular, CAR-T

Worldwide Clinical Trials•Research Triangle Park, NC

22h•$112,000 - $222,000•Remote

About The Position

Worldwide Clinical Trials is a global, midsize CRO that pushes boundaries and innovates to find cures for diseases. We are a team of over 3,500+ experts dedicated to improving lives. Our mission is to work with passion and purpose every day. We believe everyone plays an important role in making a world of difference for patients and their caregivers. We prioritize cultivating a diverse and inclusive environment that promotes collaboration and creativity. We are a workplace where people thrive by being themselves and are inspired to do their best work every day. Clinical Operations Site Management at Worldwide involves Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) who ensure clinical research programs are executed with quality and excellence. These roles are the backbone of every strong CRO, driving scientific research and leading clinical trials. We offer an uncommon experience with a team unlike any other, balancing fun with the serious business of changing lives. Our values-driven culture empowers team members to treat every trial as if a patient’s life depends on it. Our leaders are committed to advancing science and moving mountains for our customers.

Requirements

Excellent interpersonal, oral, and written communication skills in English
Ability to lead and motivate a team remotely
Demonstrate initiative and problem-solving skills by offering solutions when obstacles are identified
Strong customer focus, ability to interact professionally with a sponsor contact
Proficiency in Microsoft Office, CTMS, and EDC Systems
Bachelor’s Degree or a Nursing Degree required
2+ years’ experience as a Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role
4+ years’ experience as a Clinical Research Associate
Cardiovascular experience is required
Candidates must reside in the continental United States
Willingness to travel up to 30%

Nice To Haves

CAR-T experience is strongly preferred

Responsibilities

Provide leadership and direction to clinical site management team members from study start through to closure
Serve as Site Management’s primary point of contact and representative for clinical monitoring and site activities within the project, including, but not limited to Primary Sponsor Contact
Manage monitoring deliverables to achieve the study budget and identify out-of-scope activities