Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of almost 2,500 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

The Director of Clinical Operations is responsible for the oversight of the Clinic, Regulatory Department, Clinical Research Coordinator Department, Data Entry Department, Nutrition Department, and Clinic Scheduling Department to support the execution of Phase I studies at Worldwide Clinical Trials Early Phase Services (Worldwide) in-house facilities. The Director of Clinical Operations works under the direct supervision and guidance of the SVP, Clinical Operations for Early Phase.

What you will do:

The Director of Clinical Operations must keep abreast of all changes in study timelines and act accordingly and proactively to resolve any staff training, staff scheduling or procedure issues.

• Oversees all clinical operational departments to support clinical trials management for Phase I-IIB clinical trials, focusing on the direct events related to the protocols.
• Oversees the management of staff, including Clinic, Regulatory Department, Clinical Research Coordinator Department, Data Entry Department, Nutrition Department and Clinic Scheduling Department and maintains department budgets.
• Partners with Leadership to review studies for feasibility and provide feedback regarding scheduled workload for clinic.
• Support Business Development Group when indicated, to promote the capabilities and services of Worldwide Phase I unit.
• Reviews quality reports as appropriate, investigates any action items and ensures remediation.

What you will bring to the role

• Strong interpersonal & communication skills, sound leadership skills
• Excellent attention to detail and sound judgement
• Exceptional organizational and planning skills
• Able to project and coordinate Clinic and study needs in advance
• In-depth knowledge of the clinical research process, including Good Clinical Practices and ICH guidelines

Your experience (Change this to the specific role)

• Bachelors Degree or equivalent year of experience, preferably in the field of Life Sciences or Health
• At least 10 years of Clinical Research experience (preferably Phase I)
• Minimum 5 years of managerial experience
• Strong aptitude for verbal and written communication, presentation and relationship development
• Proven track record of Operational Excellence
• Ability to prioritize and respond appropriately to multiple demands
• Possible physical demands include, but are not limited to: lifting and carrying of objects weighing 5-50 lbs., hearing, seeing, gross and fine motor use of upper extremities, kneeling, walking, standing, leaning over for extended periods of time, squatting, eye strain/fatigue, climbing, pushing, pulling, reaching, and exposure risk to potentially infectious blood and/or body fluids, and/or hazardous fumes or chemicals.

Why Worldwide

At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every clinical trial like a patient’s life depends on it - because it does. Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.

Interested in hearing more about Worldwide or our roles? Check out our careers page at www.worldwide.com/careers !