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Clinical Research Coordinator I

Lincoln, NE, USA|Travel, Onsite

Job Overview

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Employment Type

Full-time
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Compensation

Type:
Hourly
Rate:
Range $23.00 - $31.00
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Work Schedule

Flexible
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Benefits

Medical insurance
Dental Insurance
Vision Insurance
Paid Time Off
company holidays
401(k) retirement plan
Annual Incentive Program

Job Description

Velocity Clinical Research is an established and integrated research site organization dedicated to excellence in patient care and the generation of high-quality clinical trial data. As a leader in the clinical research industry, Velocity Clinical Research is committed to advancing medical innovation by facilitating the development of novel treatments for patients through meticulously conducted clinical trials. The organization is deeply invested in aligning its core values and behaviors to empower its employees to deliver on its brand promise: bringing innovative medical treatments to patients in need. Employees at Velocity are considered integral to its mission of fostering successful clinical trials... Show More

Job Requirements

  • Phlebotomy if applicable and required by state law
  • Intramuscular dose administration and preparation if applicable and required by state law
  • Demonstrated knowledge of medical terminology
  • Demonstrated ability in the use of computers, Microsoft Office software, fax, copier, and multi-line telephone
  • Ability to work in a fast-paced environment
  • Strong verbal, written, and organizational skills
  • Excellent interpersonal and communication skills
  • Ability to work as a team player
  • Proficient in reading, writing, and speaking English
  • Ability to multi-task
  • Ability to follow written guidelines
  • Ability to work independently, plan and prioritize with some guidance
  • Flexibility to adapt as daily schedule may change rapidly
  • Attention to detail
  • Problem solving and strategic decision making ability
  • Professionalism and responsibility for individual actions
  • Ability to sit or stand for long periods of time
  • Ability to travel locally and nationally
  • Ability to communicate in person and by telephone
  • Ability to perform limited walking
  • Ability to lift up to 30 pounds

Job Qualifications

  • Bachelor’s degree with 1 year of relevant experience in the life science industry
  • Associate’s degree with 2 years of relevant experience in the life science industry
  • High school graduate and/or technical degree with minimum of 3 years relevant experience in the life science industry

Job Duties

  • Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH guidelines and Velocity’s SOPs
  • Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing and reporting adverse events, serious adverse events and deviations, implementing new protocol amendments, providing all close out reports
  • Implement research and administrative strategies to successfully manage assigned protocols
  • Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs and vendors
  • Apply good documentation practices when collecting and correcting data, transferring data to sponsor/CRO data capture systems and resolving queries
  • Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information
  • Ensure patient safety is upheld and all adverse events, serious adverse events and adverse events of special interest are followed and reported in accordance with the protocol and Velocity SOPs

Job Qualifications

Experience

Entry Level (1-2 years)

Job Location

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