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CenExelPosted 22 days ago

Clinical Research Coordinator

Full-time
On-site
Entry level
Competitive
Posted 22 days ago

Responsibilities Assists with coordinating all aspects of patient involvement from study initiation until study completion Organizes research information for clinical trials Observes subjects and assists with data analysis and reporting Schedules the collection of data Documents adverse events, protocol deviations, and other unanticipated problems appropriately Reports research data to maintain quality and compliance

Posted
22 days ago
Source
recruiting2.ultipro.com
Sector
Healthcare

Opens the employer's application page in a new tab

Responsibilities

  • Assists with coordinating all aspects of patient involvement from study initiation until study completion
  • Organizes research information for clinical trials
  • Observes subjects and assists with data analysis and reporting
  • Schedules the collection of data
  • Documents adverse events, protocol deviations, and other unanticipated problems appropriately
  • Reports research data to maintain quality and compliance
  • Performs administrative and regulatory duties related to the study as appropriate
  • Participates in other protocol development activities
  • Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
  • Educates potential participants and caregivers on protocol specific details and expectations
  • Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned)
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive

Qualifications

  • 0-3 years of experience in the medical field
  • Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials
  • Strong leadership and mentorship skills
  • Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level
  • Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations
  • Works independently as well as functioning as part of a team
  • Must be able to effectively communicate verbally and in writing

Preferred

  • Bachelors Degree

Required skills

Crisis Management

Nice to have

Bachelors Degree

Full job description

Responsibilities

  • Assists with coordinating all aspects of patient involvement from study initiation until study completion
  • Organizes research information for clinical trials
  • Observes subjects and assists with data analysis and reporting
  • Schedules the collection of data
  • Documents adverse events, protocol deviations, and other unanticipated problems appropriately
  • Reports research data to maintain quality and compliance
  • Performs administrative and regulatory duties related to the study as appropriate
  • Participates in other protocol development activities
  • Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
  • Educates potential participants and caregivers on protocol specific details and expectations
  • Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned)
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive

Preferred

  • Bachelors Degree

Benefits

  • An exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance
  • Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k for full time employees after 30 days of employment
  • CenExel is a clinical research site network supporting phase I-IV clinical trials. It is a sub-organization of Webster Equity Partners.
  • Salt Lake City, Utah, USA
  • http://www.CenExelresearch.com
  • Late Stage
  • Total Funding
  • unknown
  • 2025-04-12
  • Acquired
  • 2023-04-01
  • Private Equity
  • Leadership Team
  • Sybrand Pretorius
  • Chief Executive Officer (CEO)
  • Recent News
  • PR Newswire
  • CenExel Appoints Bethany Sensenig as Chief Financial Officer
  • 2026-06-18
  • CenExel Pain Task Force Innovates Research Approach for Next Generation, Non-Opioid Pain Therapies
  • 2026-06-11
  • CenExel highlights industry-leading capabilities amid growing FDA momentum advancing psychedelic clinical research
  • 2026-05-27
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Qualifications

  • 0-3 years of experience in the medical field
  • Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials
  • Strong leadership and mentorship skills
  • Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level
  • Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations
  • Works independently as well as functioning as part of a team
  • Must be able to effectively communicate verbally and in writing
  • Bachelors Degree
  • 0-3 years of experience in the medical field.

Required skills

  • Crisis Management

Preferred skills

  • Bachelors Degree

Experience

  • Entry level

Job details

Employment type

Full-time

Seniority level

Entry level

Date posted

Oct 22, 2026

Work mode

On-site

Job source

recruiting2.ultipro.com

Company

  • United States
  • Healthcare

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