Velocity Clinical Research, Inc. Jobs Hiring Now
Velocity Clinical Research, Inc. is hiring for 18 open roles on Migrate Mate as of July 16, 2026, concentrated in biotech & life sciences and clinical trials. Migrate Mate updates Velocity Clinical Research, Inc.'s live openings daily. Velocity Clinical Research, Inc. is a clinical research organization that operates dedicated research sites conducting pharmaceutical and medical device trials.
Find Velocity Clinical Research, Inc. JobsOverview
Velocity Clinical Research, Inc. hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 18
- Top team
- Biotech & Life Sciences
- Seniority
- Across all levels
- Work type
- 0% remote or hybrid
- Top location
- Omaha
Open Roles at Velocity Clinical Research, Inc.
Showing 18 of 18+ Velocity Clinical Research, Inc. jobs
Manager, Clinical Site
We won't show you this job again
New 7h ago
Velocity Clinical Research, Inc.
Manager, Clinical Site
Anderson, South Carolina
New 7h ago
Senior Clinical Research Coordinator
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Added 2d ago
Velocity Clinical Research, Inc.
Senior Clinical Research Coordinator
Seattle, Washington
Added 2d ago
Sub Investigator
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Added 6d ago
Velocity Clinical Research, Inc.
Sub Investigator
Beachwood, Ohio
Added 6d ago
Clinical Research Coordinator I
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Added 3w ago
Velocity Clinical Research, Inc.
Clinical Research Coordinator I
Hampton, Virginia
Added 3w ago
Clinical Research Coordinator I
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Added 3w ago
Velocity Clinical Research, Inc.
Clinical Research Coordinator I
Hampton, Virginia
Added 3w ago
Clinical Research Coordinator II
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Added 1mo ago
Velocity Clinical Research, Inc.
Clinical Research Coordinator II
Mobile, Alabama
Added 1mo ago
Clinical Research Coordinator I
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Added 1mo ago
Velocity Clinical Research, Inc.
Clinical Research Coordinator I
Edgewater, Florida
Added 1mo ago
Clinical Research Coordinator I
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Added 1mo ago
Velocity Clinical Research, Inc.
Clinical Research Coordinator I
Raleigh, North Carolina
Added 1mo ago
Executive Assistant, Legal
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Added 1mo ago
Velocity Clinical Research, Inc.
Executive Assistant, Legal
Durham, North Carolina
Added 1mo ago
Principal Investigator
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Added 1mo ago
Velocity Clinical Research, Inc.
Principal Investigator
East Greenwich, Rhode Island
Added 1mo ago
Sub Investigator
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Added 1mo ago
Velocity Clinical Research, Inc.
Sub Investigator
Spartanburg, South Carolina
Added 1mo ago
Senior Clinical Research Coordinator
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Added 1mo ago
Velocity Clinical Research, Inc.
Senior Clinical Research Coordinator
Raleigh, North Carolina
Added 1mo ago
Sub Investigator
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Added 2mo ago
Velocity Clinical Research, Inc.
Sub Investigator
Omaha, Nebraska
Added 2mo ago
Sub Investigator
We won't show you this job again
Added 2mo ago
Velocity Clinical Research, Inc.
Sub Investigator
Omaha, Nebraska
Added 2mo ago
Principal Investigator
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Added 2mo ago
Velocity Clinical Research, Inc.
Principal Investigator
Albuquerque, New Mexico
Added 2mo ago
Senior Clinical Research Coordinator
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Added 2mo ago
Velocity Clinical Research, Inc.
Senior Clinical Research Coordinator
Dallas, Texas
Added 2mo ago
Principal Investigator
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Added 2mo ago
Velocity Clinical Research, Inc.
Principal Investigator
West Jordan, Utah
Added 2mo ago
Sub Investigator
We won't show you this job again
Added 3mo ago
Velocity Clinical Research, Inc.
Sub Investigator
Los Angeles, California
Added 3mo ago
New 7h ago
Manager, Clinical Site
Velocity Clinical Research, Inc.·Anderson, South Carolina
Job functions:
Bachelor's degree
201-500 employees
Job Description
Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.
As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.
Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.
Job Summary:
The Manager, Site Operations is responsible for managing the clinical operations staff, training and onboarding of new staff, managing quality and compliance of clinical Work closely with and in support of the Site Director. Able to perform coordinator as well as supervisor duties and fill in during the absence of site coordinators. Able to function as lead coordinator on select protocols. Must be able to work independently and with all staff and customer levels.
Duties/Responsibilities:
- Work with the Site Director to meet/exceed the site’s financial, operational and study-specific targets.
- Support the identification of strategies to expand the research capabilities at the site - in line with the overall site business plan.
- Support the implementation and maintenance of VCR quality standards at the site ensuring that the conduct of clinical studies and the collection of patient data is in accordance with ICH GCPs.
- Work with the Site Director to address any study and/or clinical quality related matters.
- Ensure timely and appropriate communications occur with Sponsors and IRBs as necessary.
- Support the development of site staffing plans to ensure the successful and efficient conduct of research studies. Identify and fulfil any site resource needs which are necessary to successfully conduct and/or recruit research studies.
- Support or lead the development of the patient recruitment plan and patient outreach process for studies. Make ongoing adjustments/modifications to recruitment strategies based upon the timely review of results to ensure study-specific targets are being met.
- Manage the performance of site staff members, delegating appropriate and challenging assignments to encourage growth, development and responsibility. Responsible for supporting the ongoing training needs of site staff members are met.
- Communicate performance expectations and guidelines to site staff members.
- Identify and manage issues, concerns and problems related to staff conduct and performance.
- Identify and build relationships with outside medical practices, pharmacies, and other healthcare professionals/organizations to aid in the patient recruitment process.
- Support business development activities on behalf of the site and VCR with sponsors, CROs,CRAs and any third-party study vendors, as appropriate.
- Share best practices with other VCR site locations with the goal of raising the overall level of operational competencies at VCR.
- Support the completeness, accuracy and timeliness of Feasibility Questionnaires, CDAs, CVs and essential regulatory documents from study start-up phase until site initiation.
- Attend industry and VCR meetings relevant to the position of Manager, Site Operations.
- Manage facility and IT needs to ensure smooth and efficient operations
- Other duties as assigned
Required Skills/Abilities:
- Expertise in project management
- Knowledge of field organizational strategies
- Extensive knowledge of clinical research
- Strong communication and presentation skills
- Able to generate business correspondence, create forms and generate reports as required
- Practices professionalism and integrity in all actions
- Demonstrated ability to foster concepts of teamwork, cooperation, self- control, and flexibility to get the work done
- Ability to communicate effectively in English (both verbal and written)
- Up to 10% travel, as needed, for project team meetings, client presentations and other professional meetings/conferences as needed.
- Other duties as assigned
Education and Experience:
- Bachelor’s degree preferred; Advanced degree suggested or equivalent clinical research experience.
- 5+ years of clinical management experience or equivalent applicable experience in clinical research industry
Physical Requirements:
- Prolonged periods of sitting at a desk and working on a computer.
- Must be able to lift up to 15 pounds at times.
NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required. Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change. All employees are expected to perform their duties within their ability as required by the job and/or as requested by management
Velocity Clinical Research, Inc.
Manager, Clinical Site
Anderson, South Carolina
New 7h ago201-500 employees
Job functions:
Bachelor's degree
Job Description
Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.
As an employee of Velocity, you are the most integral part of our mission. For talented candidates who perform at a high level, Velocity will invest to support career advancement and reward performance. Whether you are new to clinical research or are an industry veteran, we invite you to apply to Velocity.
Benefits include medical, dental and vision insurance, paid time off and company holidays, 401(k) retirement plan with company-match, and an annual incentive program.
Job Summary:
The Manager, Site Operations is responsible for managing the clinical operations staff, training and onboarding of new staff, managing quality and compliance of clinical Work closely with and in support of the Site Director. Able to perform coordinator as well as supervisor duties and fill in during the absence of site coordinators. Able to function as lead coordinator on select protocols. Must be able to work independently and with all staff and customer levels.
Duties/Responsibilities:
- Work with the Site Director to meet/exceed the site’s financial, operational and study-specific targets.
- Support the identification of strategies to expand the research capabilities at the site - in line with the overall site business plan.
- Support the implementation and maintenance of VCR quality standards at the site ensuring that the conduct of clinical studies and the collection of patient data is in accordance with ICH GCPs.
- Work with the Site Director to address any study and/or clinical quality related matters.
- Ensure timely and appropriate communications occur with Sponsors and IRBs as necessary.
- Support the development of site staffing plans to ensure the successful and efficient conduct of research studies. Identify and fulfil any site resource needs which are necessary to successfully conduct and/or recruit research studies.
- Support or lead the development of the patient recruitment plan and patient outreach process for studies. Make ongoing adjustments/modifications to recruitment strategies based upon the timely review of results to ensure study-specific targets are being met.
- Manage the performance of site staff members, delegating appropriate and challenging assignments to encourage growth, development and responsibility. Responsible for supporting the ongoing training needs of site staff members are met.
- Communicate performance expectations and guidelines to site staff members.
- Identify and manage issues, concerns and problems related to staff conduct and performance.
- Identify and build relationships with outside medical practices, pharmacies, and other healthcare professionals/organizations to aid in the patient recruitment process.
- Support business development activities on behalf of the site and VCR with sponsors, CROs,CRAs and any third-party study vendors, as appropriate.
- Share best practices with other VCR site locations with the goal of raising the overall level of operational competencies at VCR.
- Support the completeness, accuracy and timeliness of Feasibility Questionnaires, CDAs, CVs and essential regulatory documents from study start-up phase until site initiation.
- Attend industry and VCR meetings relevant to the position of Manager, Site Operations.
- Manage facility and IT needs to ensure smooth and efficient operations
- Other duties as assigned
Required Skills/Abilities:
- Expertise in project management
- Knowledge of field organizational strategies
- Extensive knowledge of clinical research
- Strong communication and presentation skills
- Able to generate business correspondence, create forms and generate reports as required
- Practices professionalism and integrity in all actions
- Demonstrated ability to foster concepts of teamwork, cooperation, self- control, and flexibility to get the work done
- Ability to communicate effectively in English (both verbal and written)
- Up to 10% travel, as needed, for project team meetings, client presentations and other professional meetings/conferences as needed.
- Other duties as assigned
Education and Experience:
- Bachelor’s degree preferred; Advanced degree suggested or equivalent clinical research experience.
- 5+ years of clinical management experience or equivalent applicable experience in clinical research industry
Physical Requirements:
- Prolonged periods of sitting at a desk and working on a computer.
- Must be able to lift up to 15 pounds at times.
NOTE: The above Job Description is intended to communicate the general function of the mentioned position and by no means should be considered an exhaustive or complete outline of the specific tasks and functions that will be required. Additionally, specific tasks and duties of the position are subject to change as the Company, the department and circumstances change. All employees are expected to perform their duties within their ability as required by the job and/or as requested by management
Job Roles at Velocity Clinical Research, Inc.
Biotech & Life Sciences8 jobs
Clinical Trials2 jobs
Clinical Support2 jobs
Product Management1 jobs
Data Analytics1 jobs
Business Operations1 jobs
Healthcare Administration1 jobs
Compliance & Legal1 jobs
Working at Velocity Clinical Research, Inc.
Velocity Clinical Research, Inc.'s 18 open roles are across all levels, and about 0% are remote or hybrid. The most active teams are biotech & life sciences, clinical trials, and clinical support. Velocity Clinical Research, Inc. is a clinical research organization that staffs and operates dedicated research sites for pharmaceutical, biotechnology, and medical device studies. Roles span clinical coordination, physician investigation, and administrative support across its site network. Most Velocity Clinical Research, Inc. roles are based in Omaha, with some in Hampton and Raleigh.
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Browse jobs by roleVelocity Clinical Research, Inc. Jobs: Frequently Asked Questions
How many jobs is Velocity Clinical Research, Inc. hiring for right now?
Velocity Clinical Research, Inc. is hiring for 18 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in biotech & life sciences and clinical trials. Roles range from clinical research coordinators to physician investigators and administrative positions, so there are openings across multiple functions within the organization.
What kinds of roles does Velocity Clinical Research, Inc. hire for?
The most active teams are biotech & life sciences, clinical trials, and clinical support. Velocity Clinical Research, Inc. regularly hires for clinical research coordinator positions at multiple experience levels, sub-investigator and principal investigator roles for physician-level staff, and administrative roles such as executive assistant and legal support. Most postings are across all levels, with coordinator and investigator titles making up the core of clinical hiring.
Are Velocity Clinical Research, Inc. jobs remote or in-person?
Mostly on-site. About 0% of Velocity Clinical Research, Inc.'s open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Omaha. Each Velocity Clinical Research, Inc. listing shows its work location so you can filter before applying.
How do I apply to a job at Velocity Clinical Research, Inc.?
Find a Velocity Clinical Research, Inc. role that fits your background on Migrate Mate, then follow the listing through to Velocity Clinical Research, Inc.'s own careers page to complete the application. Velocity Clinical Research, Inc. manages its own hiring process, including screening, interviews, and offers, directly with candidates.
Does Velocity Clinical Research, Inc. hire entry-level?
Most of Velocity Clinical Research, Inc.'s open roles on Migrate Mate are across all levels as of July 16, 2026. Check individual Velocity Clinical Research, Inc. listings for stated experience requirements.
Where is Velocity Clinical Research, Inc. hiring?
Most Velocity Clinical Research, Inc. roles are based in Omaha, with some in Hampton and Raleigh, and about 0% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.