Clinical Data Manager

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!

What you'll be doing:

• Study Design & Standards
  • Independently designs CRFs and standard documentation
  • Reviews protocols and identifies basic study plan issues
• Study Build & Start-Up
  • Assists with data import setup and standard report development
  • Supports EDC design/testing, creates edit checks, and performs UAT
  • Drafts templates and guidelines with minimal supervision
• Data Review, Cleaning & Reconciliation
  • Leads data review planning and execution
  • Manages query workflows and SAE reconciliation
  • Identifies trends and prepares review meeting materials
• Data Acquisition & Integrations
  • Supports integration setup/testing and manages lab ranges
  • Handles standard vendor data and flags discrepancies
• Reporting, Lock & Closeout
  • Executes lock checklist and data verification
  • Reviews PDF packages and supports TMF readiness
• Quality, Risk & Compliance
  • Improves processes, updates documents, and supports audits
  • Applies RBQM and QbD principles
• Project & Stakeholder Management
  • Manages tasks across multiple projects and timelines
  • Prepares reports, tracks KPIs, and coordinates cross-functional teams
  • Handles vendor interactions and supports change initiatives
• Leadership & Growth
  • Onboards and mentors new team members
  • Provides informal leadership and peer support
• General Expectations
  • Attends in-person meetings as required
  • Demonstrates Rho’s Core Values and delivers excellent customer service
  • Communicates professionally and promptly
  • Maintains confidentiality and takes initiative
  • Performs other duties as assigned

• BA/BS degree along with at least 2-5 years of clinical data management experience and experience working in clinical trials databases in a commercially available EDC system (e.g. Rave, Medrio, Red Cap,…