Part-Time Clinical Research Coordinator - Patient-Focused Trials

Actalent; Glenview (IL); Presencial; USD 41 000 - 55 000; Tempo parcial

Vantagens oferecidas por esta oferta de emprego

Medical benefits

401(k) plan

Paid time off

Resumo da oferta

Actalent is seeking a part-time Clinical Research Coordinator in Glenview, IL to support clinical trials within a clinic setting. You will coordinate trial activities, assist with patient recruitment and informed consent, and ensure regulatory compliance and accurate documentation.

You will maintain study data in EDC/EMR systems, support regulatory submissions, and liaise with investigators and staff. 16–24 hours/week with on-site presence in a professional clinic environment.

Qualificações

• Minimum 12 months experience as CRC or in a related clinical research role.
• Strong understanding of clinical trial processes including start-up, recruitment, consent, screening, enrollment and follow-up.
• Solid knowledge of GCP guidelines and applicable regulatory requirements.
• Demonstrated experience with chart review and patient recruitment in clinical/research settings.
• Proficiency with EDC systems and EMR platforms.
• Ability to maintain regulatory and study documentation in compliance with protocols.
• Excellent organizational skills to manage multiple tasks and timelines.
• Strong problem-solving and attention to detail for high-quality data.
• Effective verbal and written communication with participants, investigators, and cross-functional teams.
• Strong interpersonal skills to build rapport with patients and staff.
• Proficiency in Microsoft Office (Word, Excel, Outlook).
• Ability to learn CTMS and related research platforms.

Responsabilidades

• Coordinate and implement clinical trial activities per study protocols including recruitment and enrollment.
• Conduct chart reviews to pre-screen potential participants based on eligibility criteria.
• Support recruitment by communicating with prospective participants and guiding informed consent.
• Maintain accurate regulatory files in compliance with GCP and regulations.
• Oversee data collection and entry into study databases/EDC systems with quality control.
• Use EMR systems to obtain and verify clinical information for procedures.
• Assist with regulatory documents and IRB communications, including amendments and safety reports.
• Serve as a liaison among study site, participants, investigators, and internal teams.
• Manage logistics for study visits and ensure availability of materials and supplies.
• Support procedures such as phlebotomy within scope of training when applicable.
• Monitor study activities for adherence to protocol and report deviations timely.
• Provide mentorship to junior staff and share best practices in clinical research.

Conhecimentos

CRC experience

Clinical trial processes

GCP compliance

Chart review

EDC proficiency

EMR platforms

Regulatory documentation

CTMS familiarity

Microsoft Office

Communication skills

Organizational skills

Problem-solving

Team collaboration

Phlebotomy (within scope)

Ferramentas

CTMS

EMR

EDC systems

Descrição da oferta de emprego

Actalent is seeking a part-time Clinical Research Coordinator in Glenview, IL to support clinical trials within a clinic setting. You will coordinate trial activities, assist with patient recruitment and informed consent, and ensure regulatory compliance and accurate documentation.

You will maintain study data in EDC/EMR systems, support regulatory submissions, and liaise with investigators and staff. 16–24 hours/week with on-site presence in a professional clinic environment.