Clinical Trial Recruiter

Innovo Research is a healthcare research organization conducting clinical research and trials. The Clinical Trial Recruiter identifies, recruits, screens, and consents eligible participants while supporting compliant enrollment and patient communication. This fully on-site role also maintains recruitment records, coordinates with multidisciplinary teams, and schedules patient appointments.

What you'll do:

• Identify potential research participant candidates utilizing various channels including medical records, databases, referrals, and community outreach to identify potential candidates for participation in clinical research studies
• Develop and implement effective recruitment strategies to attract eligible patients to participate in clinical research, ensuring adherence to study protocols and regulatory requirements
• Educate potential participants and their families about the purpose, procedures, risks, and benefits of the clinical trial, providing clear and accurate information to facilitate informed decision-making
• Obtain informed consent (if required and appropriately delegated) from eligible participants according to established guidelines and protocols, ensuring comprehension and compliance with ethical standards and regulatory requirements
• Conduct thorough screenings and assessments to determine initial patient eligibility for participation in clinical trials, coordinating with healthcare professionals as needed to verify medical history and suitability
• Maintain detailed and accurate records of patient interactions, recruitment efforts, and consent processes in accordance with regulatory standards and study protocols
• Collaborate closely with interdisciplinary team members including investigators, research coordinators, healthcare providers, and administrative staff to facilitate seamless recruitment and enrollment processes
• Provide ongoing support and communication to potential participants, addressing any concerns or questions they may have and ensuring compliance with study protocols
• Adhere to all relevant regulatory guidelines, institutional policies, and ethical standards governing the conduct of screening, recruitment, and enrollment in clinical research, prioritizing patient safety, privacy, and confidentiality
• Participate in training programs, workshops, and professional development opportunities to enhance recruitment strategies, communication skills, and knowledge of clinical trial protocols and regulations
• Use employee calendars to schedule appointments for patients
• Performs all additional duties as assigned

What they're looking for:

• Ability to work on site Monday-Friday
• Excellent communication, interpersonal, and organizational skills
• Ability to work effectively both independently and as part of a multidisciplinary team
• Proficiency in medical terminology, electronic health records, and data management systems
• Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time
• Bachelor's degree preferred
• Prior experience in sales, cold-calling, clinical research, patient recruitment, or healthcare-related field preferred
• Strong understanding of clinical trial protocols, regulatory requirements, and ethical guidelines preferred
• Demonstrated commitment to patient advocacy, safety, and confidentiality, preferred

Benefits:

• Health Insurance
• Dental Insurance
• Disability Insurance
• Life Insurance
• Paid Time Off
• Vision Insurance