Bilingual Clinical Research Coordinator – Part-Time

Actalent; Greenville (TX); On-site; USD 34,440,000 - 44,083,000; Part time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan - Pre-tax and R

Life Insurance (Voluntary Life & AD&D)

Short and long-term disability

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

Time Off/Leave (PTO)

Job summary

Actalent is seeking a Part-Time Clinical Research Coordinator to support a trial in the Greenville, TX area. The role involves identifying and recruiting eligible participants, educating them about the study, and ensuring engagement and protocol adherence.

Requirements include clinical research experience, strong organization, and effective communication with participants and staff. This is a part-time position around 20 hours per week, onsite in Greenville, TX.

Qualifications

• Experience as a CRC or Clinical Research Assistant.
• 1+ year of patient recruitment experience.
• 1+ years of EMR experience.
• Bilingual in Spanish and English.
• Training in HIPAA & GCP.

Responsibilities

• Review EMR to assess potential participants against inclusion/exclusion criteria.
• Pre-screen potential participants per protocol.
• Recruit and enroll participants into the trial per study protocols and regulatory requirements.
• Educate participants about the trial, procedures, expectations and follow-up.
• Conduct follow-up communications to support retention and protocol compliance.
• Schedule in-person visits and reminders; share relevant information with participants.
• Maintain accurate EMR documentation of chart reviews, screenings and interactions.

Skills

Bilingual in Spanish and English

Recruitment experience

EMR experience

Clinical research coordination

HIPAA & GCP training

Job description

Actalent is seeking a Part-Time Clinical Research Coordinator to support a trial in the Greenville, TX area. The role involves identifying and recruiting eligible participants, educating them about the study, and ensuring engagement and protocol adherence.

Requirements include clinical research experience, strong organization, and effective communication with participants and staff. This is a part-time position around 20 hours per week, onsite in Greenville, TX.