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Clinical Research Assistant Jobs

Company

Velocity Clinical Research, Inc.

Address Cincinnati, OH, United States
Employment type FULL_TIME
Salary
Category Biotechnology Research
Expires 2023-06-04
Posted at 1 year 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


  • Communicate with coworkers, leadership, study subjects, sponsors, CROs, and vendors under the direction of the Clinical Research Team
  • Process, package and ship laboratory specimens as required per protocol and IATA regulations, if applicable
  • 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
  • Understand the informed consent process with emphasis on ensuring initial and ongoing consent of study subjects
  • Cleaning, organizing, and disinfecting the patient care, lab and lab equipment areas as needed
  • 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.
  • Other duties as assigned
  • Track, order and maintain inventory of all laboratory and study related supplies throughout course of the clinical trial
  • 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
  • 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
  • Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
  • Perform front office duties as needed including but not limited to answering phones, scheduling subjects, making reminder calls and updating patient tracking systems.
  • With supervision, perform clinical assessments (vital signs, phlebotomy, ECG, etc) within scope of the protocol, local law and regulations
  • 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
  • Understand basic elements of regulatory documentation required to initiate, maintain and close a clinical research trial
  • Assist in the conduct of clinical trials in accordance with the study protocol, GCP, ICH Guidelines, and Velocity’s SOPs


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


Required Physical Abilities


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


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.