Senior Clinical Trial Manager (US)

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 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 Senior Clinical Trial Manager does at Worldwide Responsible for oversight and leading the delivery of clinical study site management activities through the co‑ordination of a team of clinical staff on particularly complex studies (such as those that have a significant global reach). Responsible for ensuring site qualification, initiation, interim monitoring, site management and study close‑out activities for studies in accordance with the study protocol and study plan. Uses data metrics and project planning to monitor and secure quality of data submitted from study sites and timely completion, including appropriate reporting and follow‑up for all safety events by site personnel. What you will do Provide leadership and direction to clinical site management team members from study start through closure. Oversee regional CTMs and coordinates efforts across the CTM team. Represent Site Management issues at Sponsor, Investigator and Bid defence meetings and act as main point of contact for activities through the study. Contribute to the overall project plan, by formulating a global monitoring strategy for site initiation, enrollment, site management and closeout phases across a given region and assigns sites on behalf of the sponsor. Provide regular input to various project tracking systems such as project financial performance reports, study metrics and trending; resource allocation to project tasks, time recognition and other systems as needed. Collaborate closely with other functions including Business Development, Regulatory, Study Start‑up and Project Management to anticipate requirements and achieve study goals. What you will bring to the role Excellent oral and written communication skills in English. Excellent planning and organisational skills with effective time management. Excellent interpersonal skills with ability to work and influence across diverse cultures. Excellent presentation skills. Ability to lead and motivate assigned team dispersed remotely across time zones. Strong understanding of FDA and /or EU Directive regulations, ICH Guidelines and local regulatory requirements. Your experience Four‑year college curriculum or equivalent with a major concentration in biological, physical or health studies, a minimum experience of four 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 six years as a Senior Clinical Research Associate. Minimum 2 years relevant experience as a CTM/LCRA (or equivalent) including overseeing a CTM team. Travel required Valid current passport required Driving license required In addition to base salary, we offer a competitive benefits package depending on location. Compensation At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation. The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates): United States of America - $112,000.00 - $222,000.00. The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage. We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit or connect with us on LinkedIn. This is who we are. We’re a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever. We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we’re here, you’ll get a different answer. And that’s what makes us special. #J-18808-Ljbffr Worldwide Clinical Trials Holdings, Inc.