Clinical Trial Manager - US

Worldwide Clinical Trials • Research Triangle Park, NC

3d

About The Position

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 over 3,500+ 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. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! What the Clinical Operations Department does at Worldwide Embark on a fulfilling Clinical Operations career as you leave a lasting impact on patients’ lives. Join Worldwide Clinical Trials for an unparalleled CRO experience, where you can drive extraordinary scientific breakthroughs and contribute to the very heart of every successful clinical trial. Working alongside brilliant minds across a variety of therapeutic areas, you will have the chance to collaborate closely with top-tier colleagues from diverse backgrounds and specialties. Our commitment to advancing clinical research is cultivated in a supportive, team-oriented atmosphere, with our hands-on leadership and dedicated team members working together to innovate and solve complex challenges for our customers.

Requirements

• Excellent interpersonal, oral, and written communication skills in English and in local language
• 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 within a sponsor contact
• Proficiency in Microsoft Office, CTMS, and EDC Systems
• Four-year college curriculum or equivalent with a major concentration in biological, physical or health studies and a minimum experience of 3 years as a Senior Clinical Research Associate (or equivalent), OR Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree preferred) and a minimum experience of 5 years as a Senior Clinical Research Associate, OR Minimum 6-month experience functioning as CTM/LCRA (or equivalent)
• Willingness to travel

Responsibilities

• Provide leadership and direction to clinical site management team members from study start through to closure
• Serve as Site Management primary point of contact and representative for clinical monitoring and site activities within the project, including, but not limited to: 1. Primary Sponsor contact 2. Investigator and Bid Defense Meetings 3. Internal and External study team calls 4. Project-specific Audits / Inspections
• Manage monitoring deliverables to achieve study budget and identify Out of Scope Activities
• Oversee compliance to the Clinical Monitoring Plan, including site visits, outstanding trip reports and visit follow up letters

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 501-1,000 employees