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Assistant Covance Clinical Research Jobs (NOW HIRING)

Horizon Clinical Research

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Clinical Research Assistant

Cypress, TX · On-site

$37K - $47K/yr

We are seeking an experienced and detail oriented Clinical Research Assistant (CRA) for our Cypress, TX and Houston, TX office. This is a full time position. The CRA will work under the supervision ...

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How much do assistant covance clinical research jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for assistant covance clinical research in the United States is $20.23, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $23.32 per hour, depending on experience, location, and employer.

What does an assistant Covance Clinical Research do?

An Assistant Covance Clinical Research supports clinical trials and research studies managed by Covance, a global contract research organization. Their responsibilities typically include organizing study documentation, assisting with data entry, coordinating communications between research teams, and ensuring compliance with regulatory guidelines. They play a key role in the smooth operation of clinical studies by handling administrative tasks and helping maintain accurate records. This position is crucial for ensuring that clinical trials run efficiently and meet quality standards.

What are the key skills and qualifications needed to thrive as an assistant Covance Clinical Research?

To excel as an Assistant in Covance Clinical Research, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), Microsoft Office Suite, and Good Clinical Practice (GCP) guidelines is typically required. Excellent communication, teamwork, and problem-solving abilities help you effectively support research teams and manage study documentation. These competencies are vital to ensure regulatory compliance, accurate data management, and the smooth execution of clinical trials.

What are some common challenges faced by an assistant Covance Clinical Research, and how can they be effectively managed?

As an Assistant in Covance Clinical Research, common challenges include managing multiple tasks with tight deadlines, maintaining accurate documentation, and ensuring compliance with regulatory standards. The fast-paced environment often requires strong organizational skills and attention to detail to handle various administrative and project support responsibilities simultaneously. Effective communication with clinical teams and proactive problem-solving help in addressing these challenges, allowing assistants to contribute smoothly to the progress of clinical trials.
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Assistant Covance Clinical Research jobs near you
Infographic showing various Assistant Covance Clinical Research job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $42,079 per year, or $20.2 per hour.

Clinical Research Assistant

Medovation Clinical Research LLC

Huntsville, AL • On-site

$20/hr

Full-time

Re-posted 23 days ago

Job description

Full-Time | Huntsville, AL

Launch Your Career in Clinical Research

Medovation Clinical Research is seeking an experienced, motivated Clinical Research Assistant to join our growing team in Huntsville, Alabama. This position offers the opportunity to work alongside physicians and research professionals conducting cutting-edge clinical trials that improve patient care and advance medicine.
Position Summary
The Clinical Research Assistant supports the successful execution of clinical trials by assisting with patient visits, study procedures, data collection, regulatory documentation, and participant recruitment while ensuring compliance with FDA regulations and Good Clinical Practice (GCP).
Responsibilities
  • Assist research coordinators and investigators with clinical trial visits
  • Recruit, schedule, and follow up with study participants
  • Collect and accurately document clinical research data
  • Maintain study files and regulatory documentation
  • Prepare study materials and laboratory specimens
  • Ensure compliance with study protocols and GCP guidelines
Qualifications
  • Minimum of 1 year of clinical research experience preferred
  • Bachelor's degree or healthcare-related experience preferred - premed and gap year med students encouraged
  • Strong organizational, communication, and computer skills
  • Ability to work independently in a fast-paced clinical environment
  • Experience with electronic medical records and research documentation is a plus
Why Join Medovation?
  • Competitive salary and benefits
  • Opportunity for career advancement
  • Work directly with experienced investigators and research professionals
  • Be part of a growing, mission-driven organization dedicated to bringing innovative therapies to patients
  • Support a collaborative team committed to excellence in clinical research
If you are detail-oriented, patient-focused, and passionate about advancing healthcare through clinical research, we'd love to hear from you.