RHO

Career Opportunities


Below is a list of our current career opportunities. Please click on the job title for more information, and apply from that page if you are interested.

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Job Locations US
The Project Manager II is responsible for successfully planning, implementing, and executing clinical trial projects of moderate size and complexity in compliance with Good Clinical Practices (GCP) and standard procedures agreed upon in each Sponsor contract. The Project Manager II will be responsible for all team members throughout the clinical trial and may assist Project Management staff on larger, complex, or global projects.
ID
2021-1758
Job Locations US-NC-Durham
The In-House CRA role is a core member of the project team. This position will work with the project manager, Lead CRA and travelling CRAs on a clinical trial to ensure that monitoring activities are properly supported and that critical documents are being tracked, collected, and reviewed.  This position will also be responsible for managing data entered into the clinical trials management system (CTMS) and other project tracking tools.    The In-House CRA will be responsible for assisting CRAs on query resolution and data reviews to ensure that studies operate in compliance with study protocols, Rho SOPs, ICH/GCP guidelines, and Federal Regulations. They will also be responsible for mentoring other team members.
ID
2021-1757
Job Locations US
The Senior Project Manager will provide leadership to cross-functional clinical research projects and team members. The Senior Project Manager will be responsible for providing on-time, on-budget, and high-quality project results as well as motivating, training and mentoring team members and helping develop new superior customer experiences. The successful applicant for this position will bring experience leading complex projects and developing junior staff.
ID
2021-1756
Job Locations US-NC-Durham
The Administrative Assistant will provide a wide range of complex, confidential administrative tasks to support their project teams and business groups.  Individuals in these roles must deliver excellent customer service to both internal and external clients, be a team-oriented professional with strong initiative, highly organized with exceptional attention to detail, have strong written and oral communication skills, prioritization skills and be able to work under tight deadlines. Candidates must have the ability to multi-task, have excellent inter-personal skills, maintain confidentiality and exhibit excellent judgment and sensitivity.
ID
2021-1755
Job Locations US
The Clinical Systems Analyst I serves as the TMF Specialist and is accountable for the oversight and management of assigned study-specific TMFs in accordance with Rho Procedural Documents. This role is a contributing study team member who also collaborates with functional SMEs and clients. 
ID
2021-1754
Job Locations US-NC-Durham
The Project Associate will perform a variety of complex, general and confidential administrative tasks in support of Rho’s Regulatory Strategy Team executing various integrated drug and biologic development and regulatory submissions projects.  The candidate will be expected to manage and respond to correspondence, organize files, enter data, schedule meetings, work on special projects and provide excellent customer service to both internal and external clients.  The selected candidate will also be expected to respond to requests in a timely manner and meet assigned deadlines.  This is a great opportunity for a candidate to gain experience and grow in and contribute to a dynamic Regulatory function. Potential candidates should be interested in the basics of drug development, with a desire to learn what it takes to manage the complex components of FDA submissions.    
ID
2021-1751
Job Locations US
We are seeking a, Associate, Federal Proposals and Contracts Analyst to join Rho’s Federal Business Unit, a collaborative team of professionals focused on producing quality proposals and administering federal contract awards.   The ideal candidate will be able to work across both proposal and contract administration activities
ID
2021-1746
Job Locations US-NC-Durham
The Senior/Principal QA Auditor will provide technical expertise to Rho’s Quality Assurance function. This individual will act as an independently functioning QA professional in providing quality assurance-related solutions to both internal and external customers. The Senior/Principal QA Auditor will also be responsible for building and maintaining effective working relationships throughout Rho and for mentoring QA teammates
ID
2021-1742
Job Locations US-NC-Durham
The Clinical Team Lead is integral to driving project success. This position will independently manage and lead the clinical team on select projects. This position will be responsible for providing direction to and training CRAs assigned to those projects. In addition, the clinical team lead is responsible for the oversight of all operational aspects related to the planning and management of CRA and site performance.   The Clinical Team Lead will be responsible for ensuring that sites and CRAs operate in compliance with study protocols, ICH/GCP guidelines, and Federal Regulations.   This is a remote opportunity. Candidates must be within 1 hour of a major US airport.   Required to travel 25% on average. 
ID
2021-1741
Job Locations US-NC-Durham
The Sr. Quality Risk Manager (QRM) is key to driving successful project implementation of a Risk-Based Quality Management (RBQM) strategy. The Sr. QRM will work with the project team to lead and facilitate project risk assessments, develop and maintain the Integrated Quality Risk Management Plan (IQRMP), facilitate strategic quality review meetings, and perform ongoing centralized monitoring reviews. The Sr. QRM will provide mentoring, training and oversight to junior level QRM staff. Additionally, the Sr. QRM will identify, revise, and implement changes to the overall RBQM process as needed.   The QRM is responsible for ensuring project teams develop an integrated quality risk management strategy in compliance with ICH E6R2 guidelines.    
ID
2021-1739
Job Locations US
The Clinical Research Associate I (CRA I) role is integral to ensuring project success as part of a multi-disciplinary team that provides scientific, statistical, and operations and management support for clinical trials.   This position will perform and coordinate all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and Rho Standard Operating Procedures. The CRA I will be responsible for supporting study team management, providing input into monitoring tool and process development, as well as training for newly assigned project CRAs.   This position requires up to 80% travel and is based in Durham, NC. 
ID
2021-1734
Job Locations US-NC-Durham
We are seeking an Associate Director, Contracts & Proposals to join Rho’s federal business unit, a collaborative team of professionals focused on producing quality proposals and administering federal contract awards.   The ideal candidate will be able to work across both proposal and contract administration activities and have extensive previous experience working with federally funded research projects. This position is dynamic in nature due to the evolving legislative and legal environment; therefore, it requires an ability to respond to change and reprioritize based on changing demands. Individuals who have solely focused on grants administration will not be considered.  This is an individual contributor position.
ID
2021-1730
Job Locations US
The Senior Project Manager will provide leadership for cross-functional, federally funded, clinical research projects and team members. The Senior Project Manager will manage multiple clinical studies and be responsible for providing high-quality project results as well as motivating, training and mentoring team members. The successful applicant for this position will bring experience leading complex projects and developing junior staff.
ID
2021-1729
Job Locations US
The Senior Clinical Research Associate (Sr. CRA) role is integral to driving project success. This position will perform and coordinate all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and Rho Standard Operating Procedures.   This position requires proven monitoring skills. The Sr. CRA conducts site visits to assess site adherence to protocol and regulatory requirements as well as manages required documentation. The Sr. CRA will also be responsible for ensuring the data remains audit ready and able to pass an audit by Rho, the Sponsor, or a regulatory agency.   The Senior CRA will be responsible for supporting study team management by providing input into monitoring tools and process development as well as training for newly assigned project CRAs.   Required to travel up to 80%. Applicants must live within a 60 minute commute of a US metropolitan airport.
ID
2021-1727
Job Locations US
The Clinical Research Associate II (CRA II) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and Rho Standard Operating Procedures.   This position requires proven monitoring skills. The CRA II conducts site visits to assess site adherence to protocol and regulatory requirements as well as manages required documentation.  The CRA II will also be responsible for ensuring the data remains audit ready and able to pass an audit by Rho, the Sponsor or a regulatory agency.   The CRA II will be responsible for supporting study team management by providing input into monitoring tools and process development as well as training for newly assigned project CRAs.   Required to travel is up to 80%.  Applicants must live within a 60 minute commute of a US metropolitan airport.
ID
2021-1716
Job Locations US-NC-Durham
We are seeking a Director, Contracts & Proposals to join Rho’s federal business unit, a collaborative team of professionals focused on producing quality proposals and administering federal contract awards.   The ideal candidate will be able to work across both proposal and contract administration activities and have extensive previous experience working with federally funded research projects. This position is dynamic in nature due to the evolving legislative and legal environment; therefore, it requires an ability to respond to change and reprioritize based on changing demands. Individuals who have solely focused on grants administration will not be considered.  This is an individual contributor position.
ID
2021-1709
Job Locations US-NC-Durham
The Learning and Performance Specialist I designs and develops curriculum for Rho’s Learning & Performance efforts. Duties include creating and developing face-to-face, online, and blended training modules, maintaining internal website content, developing and delivering learning experiences and trainings as appropriate and supporting the coordination of efforts across the Learning & Performance team.   As a member of the Learning & Performance team, you will work with a team of learning experts who engage with cross-functional internal teams and subject matter experts. Working in close collaboration, Learning & Performance supports internal teams both in consultation for improvement of existing processes and in leading capacity-building learning experiences.
ID
2021-1702
Job Locations US
The Senior Project Manager will provide leadership to cross-functional clinical research projects and team members. The Senior Project Manager will be responsible for providing on-time, on-budget, and high-quality project results as well as motivating, training and mentoring team members and helping develop new superior customer experiences. The successful applicant for this position will bring experience leading complex projects and developing junior staff.
ID
2021-1699
Job Locations US-NC-Durham
The Medical Officer will provide medical, clinical, and scientific advisory expertise across multiple therapeutic areas, to Rho project teams, Rho clients, and Investigators as requested.  This position is responsible for interacting with senior management, customers, and project teams to ensure the safety of subjects in clinical trials; ensure the scientific and ethical integrity of clinical trial design and conduct; provide medical input to clinical programs; and provide clinical development and regulatory input as needed.  This position is based in Research Triangle Park in Durham, NC.
ID
2021-1673
Job Locations US-NC-Durham
The Associate Director, Vendor Management will be responsible for the oversight and management of Rho’s Vendor Management Program, including creation and implementation of governance structures for priority vendors, tracking key data related to vendor assessments and vendor performance, and providing insights and recommendations to senior leadership. Strong collaboration, organization, analytical and communication skills are required. The Associate Director, Vendor Management must work effectively cross-functionally to ensure the success of the Vendor Management Program.
ID
2021-1672