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Clinical Research Coordinator

EPW Curesearch LLC

Pasadena, california


Job Details

Full-time


Full Job Description

Are you a driven and detail-oriented individual with a passion for clinical research? Look no further! EPW Curesearch LLC is seeking a Clinical Research Coordinator (CRC) to join our dedicated team in Los Angeles County, CA

In this multi-year position, you will have the opportunity to work on an active pulmonary study conducted by a major pharmaceutical sponsor. As a CRC, you will be responsible for various aspects of clinical research including participant recruitment and enrollment, scheduling study visits, carrying out study procedures, data collection and transfer to data repositories, and maintaining study records. You will work closely with the Research Program Manager and support the principal investigator (PI) in meeting protocol requirements.

We are looking for someone who can thrive in a medical clinic setting, exhibit a high degree of initiative, and possess excellent interpersonal, organizational, and time management skills.

We are currently hiring for both full-time and part-time positions, so whether you're looking for a challenging full-time role or a flexible part-time opportunity, we have options available for you!

Directly interact with clinical research participants, either in person or via telephone or telehealth.

Coordinate regulatory aspects of the trial to ensure compliance with industry standards, company policies, FDA requirements, and other medical site policies.

Schedule and coordinate study procedures as per protocol guidelines.

Screen, recruit, enroll, and follow subjects according to protocol guidelines.

Develop and maintain data collection tools, including CRFs, and assist in data entry.

Conduct study procedures as instructed by the protocol and maintain scope of work.

Assist with research billing activities if required.

Review and abstract information from medical records for verification of eligibility for trials.

Ensure patient safety by reviewing records and reporting any adverse events per protocol and HRPP standards.

Assist in the development of marketing and recruitment strategies for clinical research studies.

Develop proficiency in the clinical trial management system, electronic medical record, and other required data entry systems.

Maintain accurate and up-to-date documentation related to study activities.

EPW Curesearch LLC, as part of an integrated healthcare company, is a leading provider of clinical trial and research solutions in the U.S. We work with top medical specialists and partner with leading pharmaceutical brands to facilitate phase II & phase III interventional drug clinical trials in key therapeutic areas.

Requirements

  • Bachelor's or higher degree in a medical or science-related field.
  • At least one year of clinical research experience.
  • ACRP or SOCRA certification is a plus.
  • Strong knowledge of basic and clinical research terminology, regulations, and procedures.
  • Proficiency in computer skills, including spreadsheets, databases, and web-based software.
  • Excellent communication skills and ability to effectively interact with various stakeholders.
  • Ability to work with confidential information on a daily basis.
  • Proactive problem-solving skills and ability to work independently with minimal supervision.

Benefits

  • Paid Time Off (Vacation, Sick & Public Holidays)
  • Family Leave (Maternity, Paternity)
  • Training & Development
  • Work From Home
  • Wellness Resources

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