Clinical Trial Support Specialist

CenExel

Englewood (CO)

On-site

USD 26,000 - 29,000

Full time

41 hours ago
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Benefits offered by this job

Health Insurance
Dental
Vision
401k

Job summary

CenExel Clinical Research is seeking a Research Assistant I to support Clinical Research Coordinators in achieving protocol-specific study goals while adhering to ICH, GCP, and site guidelines.

This on-site role at CenExel involves patient chart creation, visit preparation, data entry, specimen coordination, and communication with participants and vendors. The position offers growth within a collaborative team and competitive benefits after probation.

Qualifications

  • High school diploma or equivalent.
  • Excellent computer skills and familiarity with office equipment.
  • Strong organization and record-keeping abilities.
  • Ability to communicate clearly, both verbally and in writing.
  • Ability to work on-site in an office environment.

Responsibilities

  • Create and maintain patient charts for all assigned studies.
  • Prepare participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate.
  • Maintain inventory of study-specific supplies including lab kits, assessments and participant-facing materials.
  • Timely completion of data entry and query resolution for all CRFs.
  • Conduct assessments including blood pressure and urine collection.
  • Communicate with study participants, caregivers, third-party vendors and laboratories as needed.
  • Assist Coordinators with scheduling and clerical tasks.
  • Support coordination of study monitoring visits.
  • Complete daily responsibilities delegated by CRC as they pertain to the study and participants.

Skills

Computer skills
Organizational skills
Interpersonal skills
Communication skills

Education

High school diploma

Job description

CenExel Clinical Research is seeking a Research Assistant I to support Clinical Research Coordinators in achieving protocol-specific study goals while adhering to ICH, GCP, and site guidelines.

This on-site role at CenExel involves patient chart creation, visit preparation, data entry, specimen coordination, and communication with participants and vendors. The position offers growth within a collaborative team and competitive benefits after probation.

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