Clinical Recruitment Associate

Summary: The Clinical Recruitment Associate will focus on recruiting prospective participants into research studies. They will support building community relationships with individuals, non-profit organizations, and businesses. They will set up educational events and perform community outreach to support Pinnacle Clinical Research programs.

Duties and Responsibilities

Performs all functions within company Strategic Plan, Policies, Mission, Vision, and Goals Recruits, schedules, and screens study participants using protocol criteria and manages recruitment communications Develops relationships with local healthcare and social service providers Coordinates event participation with vendors and community representatives while ensuring safety of company property Provides health education, support, and accurate information to community members and healthcare providers regarding Pinnacle Clinical Research Participates in health promotion activities including home visits, health fairs, and public events to support participant recruitment Provides Fibroscans as required and with training and certification Collects medical history and health information from patients while maintaining participant privacy and confidentiality Assists in establishing recruitment lists from electronic medical records, and internal databases Education/Experience: Associates degree in a related field; and one to two years related experience and/or training; or equivalent combination of education and experience.

Certificates and Licenses: Valid Driver’s License Knowledge, Skills, and Other Abilities: Oral and written communication skills Bilingual (Spanish strongly preferred) Organizational skills Ability to pay attention to detail People skills, including possessing a positive, friendly, and professional demeanor Ability to be flexible with changing priorities Ability to communicate in a diplomatic and professional manner Work Environment and Physical Demands: The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Work is performed in an office/laboratory and/or a clinical environment. Exposure to biological fluids and/or bloodborne pathogens. Personal protective equipment is required, such as protective eyewear, garments, and gloves.

Occasional travel may be required, domestic and/or international. Ability to work in an upright and/or stationary position for 6-10 hours per day. Frequent mobility required. Occasionally squatting, kneeling, or bending. Light to moderate lifting and carrying (or otherwise moves) objects including medical equipment with a maximum lift of 20-50 lbs.

May need to work evenings and/or weekends as needed. Perks of working at Summit Clinical Research Solutions: 401k Medical, dental, vision, long-term disability, short-term disability, FSA, and life insurance 3 weeks of paid time off 14 paid company holidays Scrub uniform voucher (specific positions apply) And more! Summit Clinical Research Solutions is an equal opportunity employer.

All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status, or any other protected Federal, State/Province, or Local status unrelated to the performance of the work involved.