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.
SUMMARY:Provideexpertiseto data management assigned projects to ensure that they are executed in an efficient,accurateandtimelymanner to the Sponsor's satisfaction.
RESPONSIBILITIES:
Tasks may include but are not limited to:
Provideoversightof data management services (start up, conduct and close out) across multiple complex globalprojects/programs, including:
Ensureappropriateresourcesareallocatedto complete all DM activities on time and budget.
Prepare DM trial documentation (DMP, DB Specifications, Edit check specifications, CCGs, DTAs).
Ensure effective UAT is performed.
Write external vendor reconciliation specifications for programming reconciliation outputs (e.g. Serious Adverse Events, IRT, Central Laboratory).
Oversee data cleaning activities.
Produce metrics tomonitorprogress of trial activities.
Ensure alldatabaselock activities are completed on time.
RepresentWorldWideDM at both internal and external study meeting calls, including providing input.
Monitor project scope, budgets and risks and alert DM Management of any concerns.
Liaise with DM Management at regular intervals to discuss progress and any issues outstanding (e.g. during Project Review Meetings).
Collaborate with internal Worldwidedepartments working on the same project.
Provide feedback on process improvements to DM Management and/or SMEs.
Participate in and lead process reviews.
Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.
SKILLS:
Excellent attention to detail.
Excellent written and verbal communication skills.
Workingknowledge of data management best practices & technologies as applied to clinical trials.
Excellent communication and interpersonal skills to collaborate with cross-functionalinternal and external teams.
Solidunderstanding of clinical trial process and protocols documents (protocols, statistical analysis plans, CRFs, study reports) and processes.
Developing analytical andproblem solvingskills.
REQUIREMENTS:
Bachelor’s degree or higher in biomedical sciences, life sciences, computerscienceor related discipline — or equivalent relevant experience.
Min of 3 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries.
Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.
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.