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CenExelPosted 30+ days ago

Research Assistant I - Clinical Research

Full-time
On-site
Entry level
Competitive
Posted 30+ days ago

Responsibilities Creating and maintaining patient charts for all assigned studies Preparing participant visits based on CRC's schedule, ensuring all source documents, assessments, lab kits, and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts Maintaining inventory of study-specific supplies, including lab kits, assessments, and

Posted
30+ Days Ago
Source
recruiting2.ultipro.com
Sector
Healthcare

Opens the employer's application page in a new tab

Responsibilities

  • Creating and maintaining patient charts for all assigned studies
  • Preparing participant visits based on CRC's schedule, ensuring all source documents, assessments, lab kits, and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts
  • Maintaining inventory of study-specific supplies, including lab kits, assessments, and participant-facing materials
  • Timely completion of data entry and query resolution for all CRFs, based on sponsor-specific timelines and deadlines established in contract or other communication
  • Assisting Coordinators in assessments, including but not limited to blood pressure, urine collection
  • Communicating with study participants, caregivers, third-party vendors, and laboratories as needed
  • Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks
  • Aiding Coordinators in the facilitation of study monitoring visits
  • Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants
  • 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

  • Interest in and knowledge of specific study indications
  • Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.)
  • Skilled in organization and record maintenance
  • Skilled in developing and maintaining effective working relationships with supervisors and co- workers
  • Strong personal initiative and attention to detail
  • Ability to react calmly and effectively in emergency situations
  • Ability to interpret, adapt and apply guidelines and procedures
  • Ability to clearly communicate both orally and verbally

Required skills

Interpersonal RelationshipsRecord Maintenance

Full job description

Responsibilities

  • Creating and maintaining patient charts for all assigned studies
  • Preparing participant visits based on CRC's schedule, ensuring all source documents, assessments, lab kits, and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts
  • Maintaining inventory of study-specific supplies, including lab kits, assessments, and participant-facing materials
  • Timely completion of data entry and query resolution for all CRFs, based on sponsor-specific timelines and deadlines established in contract or other communication
  • Assisting Coordinators in assessments, including but not limited to blood pressure, urine collection
  • Communicating with study participants, caregivers, third-party vendors, and laboratories as needed
  • Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks
  • Aiding Coordinators in the facilitation of study monitoring visits
  • Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants
  • 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

Benefits

  • An exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance.
  • A generous benefits package to full-time employees after 30 days of employment, including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
  • 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
  • Company data provided by
  • AI Tools
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Qualifications

  • Interest in and knowledge of specific study indications
  • Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.)
  • Skilled in organization and record maintenance
  • Skilled in developing and maintaining effective working relationships with supervisors and co- workers
  • Strong personal initiative and attention to detail
  • Ability to react calmly and effectively in emergency situations
  • Ability to interpret, adapt and apply guidelines and procedures
  • Ability to clearly communicate both orally and verbally

Required skills

  • Interpersonal Relationships, Record Maintenance

Experience

  • Entry level

Job details

Employment type

Full-time

Seniority level

Entry level

Date posted

Oct 13, 2026

Work mode

On-site

Job source

recruiting2.ultipro.com

Company

  • Los Angeles, CA
  • Healthcare

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