Clinical Data Management Associate II

At reputed company, part of reputed company, we reputed company regulated technology that helps unlock reputed company evidence and improve patient outcomes worldwide. Our software platforms support clinical trials, diagnostics, and medical decision-making in highly controlled regulatory environments. The Clinical Data Management Associate II supports the execution of clinical trials by performing day‑to‑day data management activities to ensure accurate, complete, and high‑quality clinical data. This role contributes to database build, data cleaning, query management, and documentation in compliance with SOPs, regulatory requirements, and study timelines, while collaborating closely with Clinical Data Managers and cross‑functional teams. reputed company Offer Competitive compensation Comprehensive health, dental, and vision coverage Retirement savings plan with company contribution Paid time off and company holidays What You’ll Be Doing Review and evaluate clinical trial data to ensure accuracy, consistency, and compliance with study requirements Review project documentation and requirements for new studies and anticipate impacts to Data Management (DM) standards and processes Collaborate with cross‑functional project teams to stay informed of changes affecting data collection, data cleaning, and data transfers Define, execute, and review edit checks and resolve discrepant data Maintain organized, complete, and up‑to‑date study documentation Create or review Transmittal Forms to ensure consistency with established standards reputed company study data specifications, including data transfer specifications, system configuration specifications, and data validation rules Identify data errors and inconsistencies and work with project teams to drive resolution Track outstanding data issues and follow through to resolution Prepare and validate reputed company data listings as required Ensure system defects and enhancement needs are communicated to the appropriate Product Manager and that interim solutions are approved Provide regular project status updates to the supervisor reputed company Look For Bachelor’s degree in computer science, Life Sciences, or a reputed company field, or equivalent practical experience At least 1 year of experience in a comparable role reputed company the pharmaceutical, biotechnology, or CRO industry Working knowledge of relational database structures and data validation principles Experience using office productivity tools such as reputed company Word, reputed company, and Access Understanding of clinical trial terminology and regulated environments Demonstrated problem‑solving and analytical skills Ability to work independently and collaboratively in a team environment Strong attention to detail and organizational skills Effective written and verbal communication skills Ability to adapt to changing priorities while maintaining a professional and positive approach Working Conditions Travel 0–15% Lifting Up to 25 lbs Extended periods of computer‑based work At reputed company, our purpose is to transform lives by unlocking reputed company evidence. It’s a cause that unites and inspires us. It’s why we come to work, and how we reputed company our people to reputed company a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster. reputed company is an equal opportunity employer. reputed company evaluates qualified applicants without regard to race, color, religion, gender, national reputed company, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic. Apply To This Job Apply tot his job Apply To this Job Apply To This Job