Job Details
Posted 16 October, 2026
Job Id: 630895
Analyst, Clinical Operations
Job Description
Target PR Range: 33-43/hr DOE
Summary:
Responsible for the coordination of case planning workflows for commercial case evaluations.
Key Responsibilities:
* Key Responsibilities:
* Oversee daily requests and support for the technical platforms used for case planning activity in partnership with the field team, case planning, sales operations, information technology and external stakeholders.
* Responsible for collaborating with the case planning team to plan, schedule, track, manage and achieve defined goals.
* Responsible for external stakeholder communication and support for the case planning workflow process.
* Coordinate project management platform tasks and process standardization.
* Drive timely and accurate imaging submissions from commercials sites to allow for internal review by the case planning team.
* Identify issues and provide recommendations for process improvement.
* Provide high quality, timely responses to the sales organization to meet information and reporting needs. Communicate complex logic and analysis in a manner that is easily understandable.
Education and Experience:
Bachelor’s Degree or Equivalent in Computer Science, Engineering, Business or related field, 2-3 year’s experience Patient screening experience in the setting of a clinical trial Required.
Additional Skills:
* Good computer skills in Microsoft Office Suite, including Word, Excel, and PowerPoint and related system(s)
* Good written and verbal communication skills and interpersonal relationship skills
* Good problem-solving, organizational, analytical and critical thinking skills
* Moderate understanding of medical terminology as it relates to clinical studies
* Ability to manage confidential information with discretion
* Strict attention to detail
* Ability to interact professionally with all organizational levels
* Ability to work in a team environment, including inter-departmental teams and representing the organization on specific projects
* Ability to build productive internal/external working relationships
* Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
Education and Experience:
* Bachelor’s Degree or Equivalent in Computer Science, Engineering, Business or related field, 2-4 year’s patient screening experience in the setting of a clinical trial Required.
???????*CO/NYC candidates might not be considered
Equal Opportunity Employer
We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
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