Clinical Data Manager

Rho Inc

7d•$70,000 - $110,000•Onsite

About The Position

Join us in redefining what it means to work for a CRO. When you work at Rho, it’s more than just a job—you become part of the Rho Factor. We’re a proud bunch of science nerds who love tackling big challenges together. We’re not your typical CRO, and we’re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do. Whether you’re a data wizard, analytical genius, project mastermind, or any other role, you’ll fit right into the equation of the Rho Factor. Expect plenty of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work—and each other. You’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career. As our next Clinical Data Manager, you will have the opportunity to work closely with the multidisciplinary project team across the life cycle of the project to ensure data management is thoughtfully planned and delivered in a consistent, timely, and high quality manner. You will be a key contributor to project success through development and utilization of innovative tools to help automate manual tasks and identify data trends in a timely fashion and constant collaboration with project peers, particularly biostatisticians, statistical programmers, and clinical operations personnel. You will also independently perform and oversee completion of data management tasks to ensure clinical database design supports project outcomes; proactively clean clinical trial data and mitigate risks; effectively communicate data-related decisions to sponsors; and ensure data management activities follow all applicable standards and project specific procedures. Our Clinical Data Managers will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group!

Requirements

BA/BS degree along with at least 2-5 years of clinical data management experience
Experience working in clinical trials databases in a commercially available EDC system (e.g. Rave, Medrio, RedCap, Veeva)
Working knowledge of an electronic data capture (EDC) system and CRF design principles
Demonstrated knowledge of data review and reconciliation process
Demonstrates effective analytical and problem-solving skills
Able to independently utilize available resources, including following Standard Operations Procedures (SOPs) and templates
Able to communicate clearly and effectively both written and verbal
Strong interpersonal skills and ability to work effectively and collaboratively within a team environment
Self-starter, able to work independently and have the ability to coordinate multiple activities simultaneously in support of various projects.
Demonstrates attention to detail and commitment to producing high quality work
Proficiency in MS Word, Excel, PowerPoint.