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Clinical Research Assistant Jobs

Company

Velocity Clinical Research, Inc.

Address West Jordan, UT, United States
Employment type FULL_TIME
Salary
Category Biotechnology Research
Expires 2023-10-12
Posted at 7 months ago
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.


Summary


  • The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities.


Role & Responsibilities


  • Perform venipuncture, capillary puncture and/or other fluid collection within scope of the protocol and local law and regulations
  • Prepare source document charts, copy and/or file medical records and study related documents as required.
  • Understand the informed consent process with emphasis on ensuring initial and ongoing consent of study subjects
  • With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations
  • Understand basic elements of regulatory documentation required to initiate, maintain and close a clinical research trial
  • Enter source data into the sponsor's and/or vendor’s data portal and resolve basic queries in a timely manner under the direction of the Clinical Research Coordinator
  • Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs
  • Understand good documentation practices when collecting, transferring data to sponsor/CRO data capture systems and resolving queries under the direction of the Clinical Research Coordinator
  • Ability to escalate potential patient safety issues such as adverse events, serious adverse events, and adverse events of special interest to the Clinical Research Team
  • Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable
  • Other duties as assigned
  • Understand and participate in patient recruiting tasks including but not limited to prescreening potential subjects for clinical research trials either via phone or in person
  • Track, order and maintain inventory of all laboratory and study related supplies throughout course of the clinical trial
  • Cleaning, organizing, and disinfecting the patient care, lab and lab equipment areas as needed
  • Perform front office duties as needed including but not limited to answering phones, scheduling subjects, making reminder calls and updating patient tracking systems.
  • Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
  • Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team


Education/Experience


  • High School Graduate and/or technical degree with minimum of 1 year of relevant experience in life sciences industry


Required Licenses/Certifications


  • Phlebotomy if applicable and required by state law
  • Intramuscular dose administration and preparation if applicable and required by state law


Required Skills


  • Demonstrated ability to use the following technology Computers, Microsoft Office software, fax, copier, and multi-line telephone.
  • Demonstrated ability to multi-task
  • Demonstrated ability to read, write, and speak English
  • Understanding of verbal, written, and organizational skills
  • Demonstrated ability to follow written guidelines
  • Demonstrated ability to work as a team player
  • Demonstrated ability to be flexible/adapt as daily schedule may change rapidly
  • Demonstrated knowledge of medical terminology


Required Physical Abilities


  • Limited walking required
  • Limited to lifting up to 30 pounds
  • Communicate in person and by a telephone
  • Sit or stand for long periods of time


Velocity is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic. We are an E-Verify Employer in the United States.