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As a culture-driven organization Catalyst Clinical Research supports our team members to ensure we deliver for our clients. Catalyst Clinical Research believes in listening to employees and clients to understand and address any challenges.

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Headshot of Ershlena McDaniel
Headshot of Ershlena McDaniel
Headshot of Ershlena McDaniel
Headshot of Ershlena McDaniel
Headshot of Ershlena McDaniel

“In the middle of a pandemic, I decided to change jobs and come to Catalyst as a Senior Project Manager. It immediately felt like the right decision. I am surrounded by a wonderful team who acknowledges my experience and encourages input based on that experience. As we have taken on larger and more difficult studies, I have witnessed how all the functional areas come together to get the job done. It is truly a team effort!”

Catalyst Senior Project Manager

Job Openings

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Clinical Development Systems Analyst

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As a Clinical Development Systems Analyst you are a key member of the Business Enablement Team. You will act as a Subject Matter Expert (SME)/Super User in the assigned systems utilized for efficient management and oversight of clinical trials. Supporting Catalyst Clinical Systems process and…
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Clinical Development Systems Analyst- United Kingdom

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As a Clinical Development Systems Analyst you are a key member of the Business Enablement Team. You will act as a Subject Matter Expert (SME)/Super User in the assigned systems utilized for efficient management and oversight of clinical trials. Supporting Catalyst Clinical Systems process and…
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Clinical Research Associate, Oncology- Spain

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As a Clinical Research Associate you will be responsible for monitoring clinical trials and ensuring investigators are conducting research within the requirements of the clinical protocol and ICH-GCP.  You will be involved in all stages of clinical trials, including the identification of an investigational site…
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Clinical Trial Lead

Raleigh

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As the Clinical Trial Lead you are responsible for oversight of the team of field Clinical Research Associates (CRA) or In-House CRAs who provide qualification, selection, monitoring, and close out of sites performing clinical trial(s).  Lead Clinical Research Associates/Clinical Trial Managers review workload requirements and…
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Principal Statistical Programmer

Raleigh

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As a Principal Statistical Programmer you will be a key member of the Clinical Development Operations, Statistical Programming Team. You will program routine and customized data displays, (including listings, tables, and graphics) in accordance with approved Statistical Analysis Plan and shell displays.  Additionally, the Principal Statistical…
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Senior Clinical Research Associate – Italy

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As a Senior Clinical Research Associate you are responsible for monitoring clinical trials and ensuring investigators are conducting research within the requirements of the clinical protocol and ICH-GCP.  You will be involved in all stages of clinical trials, including the identification of an investigational site…
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Senior Clinical Trial Associate- United Kingdom

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As a Senior Clinical Trial Associate you are responsible for providing the administrative support to the clinical development/project teams and maintaining a range of clinical documentation.  You will be focused on supporting external client teams as well as our internal Clinical Services team.  You will work closely…
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Senior Clinical Trial Associate-Spain

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As a Senior Clinical Trial Associate you are responsible for providing the administrative support to the clinical development/project teams and maintaining a range of clinical documentation.  You will be focused on supporting external client teams as well as our internal Clinical Services team.  You will work closely…
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Senior Project Manager

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As a Senior Project Manager – Oncology, you will be responsible for the routine cross-functional operations of assigned studies for one or more clients or management of a portfolio of functional projects, with minimal or no supervision. You will act as the team leader, ensuring that assigned studies are…
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Senior Safety Specialist

Raleigh

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Position Description:As the Sr. Safety Specialist (SS), you will be a key member of the Pharmacovigilance (PV) organization, responsible for coordinating and managing contracted safety responsibilities for one or more programs, including staffing, training, and procedural compliance. You will work with senior management to develop consistent internal processes and…
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Senior Statistical Programmer

Wilmington

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Duties: Develop new software applications or customize existing applications to meet specific scientific project needs. Create novel computational approaches and analytical tools as required by research goals. Consult with researchers to analyze problems, recommend technology-based solutions, or determine computational strategies. Keep abreast of new biochemistries,…
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VP, Business Development

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As The Vice President, Business Development you will be responsible for establishing and executing on the company’s Sales strategy by developing effective processes to manage sales and related activities from prospect identification through to contract signature and long-term account management.  You will be accountable for…
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