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Worldwide Clinical Trials seeks a Senior Program Clinical Data Manager to lead data management across global projects, taking ownership from study start-up through database lock and close-out. You will mentor colleagues, strengthen data management processes, and ensure high-quality data delivered on time.
This remote role is open to US-based candidates. A Bachelor’s degree or higher in a related field and a minimum of 7 years of clinical data management experience are required, with expert CDM
Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world. With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research. Make an Impact as a Program Clinical Data Manager at Worldwide
Take ownership of clinical data management across complex, global projects and programs, helping ensure high-quality data is delivered accurately, efficiently, and on time. In this senior role, you'll lead data management activities from study start-up through database lock and close-out, partnering with sponsors and cross-functional teams throughout the clinical trial lifecycle. You'll also bring your expertise beyond individual studies, serving as a subject matter expert, mentoring colleagues, strengthening data management processes, and contributing to departmental initiatives. Your leadership will help teams address risks, maintain quality, and deliver work that meets sponsor expectations.
Where You'll Work This is a remote role open to candidates based in US. You will collaborate with global teams across multiple time zones.
Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, or equivalent relevant experience, plus a minimum of 7 years of clinical data management or related experience within the pharmaceutical, biotechnology, or medical device industries. Expert knowledge of clinical data management best practices and technologies as applied to clinical trials. Advanced understanding of the clinical trial process and key documents, including protocols, statistical analysis plans, CRFs, and study reports. Strong independent leadership, analytical, and problem-solving skills, with the ability to provide autonomous oversight across complex projects. Excellent attention to detail and the ability to manage work accurately and effectively. Excellent communication and interpersonal skills for collaborating with cross-functional internal teams, sponsors, vendors, and other external partners. Proficiency in English, with strong written and verbal communication skills.
Discover the Difference We love knowing that someone is going to have a better life because of the work we do. Discover the Difference at Worldwide Clinical Trials. Explore additional opportunities on our careers page, visit http://www.worldwide.com/careers, or connect with us on LinkedIn.
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 - $99,000.00 - $196,000.00 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.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity.
We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful.
We're on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity.
We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.
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 is what makes us special.