Site Research Assistant - Houston, TX

IQVIAHouston, TX
391d$52,000 - $81,120

About The Position

The Site Research Assistant will play a crucial role in supporting clinical trial activities, ensuring compliance with applicable regulations. This position requires strong interpersonal skills, logical thinking, and the ability to adapt to changing conditions while maintaining effective communication with study team members and investigators.

Requirements

  • High School Diploma and 1 year of relevant work experience in clinical research.
  • At least 1 year experience working in a clinical research setting preferred.
  • Working knowledge of clinical trials.
  • Working knowledge of the principles of Good Clinical Practices (GCP).
  • In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
  • Skill in carrying out required clinical procedures.
  • Working knowledge of medical terminology.
  • Ability to pay close attention to detail.
  • Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.

Nice To Haves

  • Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.

Responsibilities

  • EDC Entry and Query Resolution
  • Develop strong working relationships and maintain effective communication with study team members.
  • Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office.
  • Assist with the screening, recruiting, and enrollment of research subjects.
  • Perform patient/research participant scheduling.
  • Collect patient/research participant history.
  • Coordinate follow-up care and laboratory procedures.
  • Adhere to an IRB-approved protocol.
  • Assist in the informed consent process of research subjects.
  • Support the safety of research subjects.
  • Coordinate protocol-related research procedures, study visits, and follow-up care.
  • Comply with company and Sponsor policies, standard operating procedures (SOPs), and guidelines.
  • Schedule subject visits and procedures.

Benefits

  • Potential base pay range of $25.00-$39.00 per hour, with variations based on qualifications, location, and schedule.
  • Incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare benefits.

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What This Job Offers

Job Type

Part-time

Career Level

Entry Level

Industry

Professional, Scientific, and Technical Services

Education Level

High school or GED

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