Clinical Trial Recruiter

INNOVO RESEARCH INC•Champaign, IL

1d•$40,000 - $55,000•Onsite

About The Position

Innovo Research is seeking a dedicated and compassionate Clinical Trial Recruiter to identify, recruit, and consent patients for clinical research and trials. The role supports successful enrollment of eligible participants and contributes to the development of treatments and therapies. This is a 100% on-site position at Christie Clinic in Champaign, Illinois, Monday through Friday. The role is non-exempt and eligible for overtime pay beyond the salary. Flexible hours may be needed to accommodate patient schedules and study requirements, and occasional evening and weekend work may be required. The recruiter identifies potential participants, develops recruitment strategies, explains clinical trials to patients and families, and supports screening, consent, and enrollment in accordance with protocols and applicable ethical and regulatory requirements. The role involves close collaboration with investigators, research coordinators, healthcare providers, and administrative staff, along with maintaining accurate records and protecting participant safety, privacy, and confidentiality. Innovo Research is an equal opportunity employer and provides reasonable accommodations for qualified individuals with disabilities. Applicants must be authorized to work for any employer in the United States; visa sponsorship is not available.

Requirements

Excellent communication, interpersonal, and organizational skills.
Ability to work effectively independently and as part of a multidisciplinary team.
Proficiency in medical terminology, electronic health records, and data management systems.

Nice To Haves

Bachelor's degree preferred.
Prior experience in sales, cold-calling, clinical research, patient recruitment, or a healthcare-related field preferred.
Understanding of clinical trial protocols, regulatory requirements, and ethical guidelines preferred.
Commitment to patient advocacy, safety, and confidentiality preferred.

Responsibilities

Identify potential research participants through medical records, databases, referrals, and community outreach.
Develop and implement recruitment strategies that comply with study protocols and regulatory requirements.
Explain trial purposes, procedures, risks, and benefits to potential participants and their families.
Obtain informed consent when required and appropriately delegated, following established guidelines and ethical and regulatory requirements.
Conduct remote screenings and assessments to determine initial eligibility, coordinating with healthcare professionals as needed to verify medical history and suitability.
Maintain accurate records of patient interactions, recruitment efforts, and consent processes in accordance with regulatory standards and study protocols.
Collaborate with investigators, research coordinators, healthcare providers, and administrative staff to facilitate recruitment and enrollment.
Provide ongoing communication and support to potential participants, address their questions and concerns, and ensure compliance with study protocols.
Follow regulatory guidelines, institutional policies, and ethical standards, prioritizing patient safety, privacy, and confidentiality.
Participate in training, workshops, and professional development opportunities.
Use employee calendars to schedule patient appointments.
Perform additional duties as assigned.