Participant Recruitment Agent

Altasciences•Overland Park, KS

12d•Hybrid

About The Position

The Participant Recruitment Agent I provides prospective participants with preliminary clinical trial information and details about the organization. This role is responsible for conducting pre‑screening activities to assess initial eligibility for clinical trial participation. The Participant Recruitment Agent I ensures that all tasks are performed in accordance with study protocols, Good Clinical Practices (GCP), and Standard Operating Procedures (SOPs).

Requirements

High School Diploma or GED required with 6 months of related experience required
Must have strong computer literacy with experience with the Microsoft suite
Ability to read and interpret technical documents and industry specific manuals.
Strong verbal communication and interpersonal skills, with the ability to interact professionally with diverse populations.
Excellent verbal and written communication skills.
Ability to handle high call volumes and work in a fast-paced environment.
Active listening and problem-solving skills.
Time management skills and ability to sort through conflicting priorities.
Demonstrated patience and customer-focused mindset.
Personal/professional integrity and proven discretion in handling confidential information.
Demonstrated attention to detail and accuracy.
Must be self-directed, motivated, and have a willingness to take the initiative to identify and anticipate client needs and make recommendations for implementation.
Applicants must be legally authorized to work in the United States.
Altasciences is unable to provide sponsorship, sponsorship transfers, or visa maintenance for this position.
All applicants must possess valid work authorization that does not require employer sponsorship now or in the future.

Nice To Haves

Bilingual English and Spanish would be a bonus!

Responsibilities

Provide prospective participants with introductory information about clinical trials, including study expectations, visit requirements, and organizational details.
Answer questions from participants and guide them through the initial steps of the recruitment process.
Answer in-coming calls and internet applications/web submission forms from clinical trial participants.
Contact past/potential participants to provide upcoming clinical trial information and determine eligibility.
Maintain a professional and welcoming demeanor to support a positive participant experience.
Schedule screening and/or other clinical trial related appointments.
Update participant management software with participant information (ex. demographics and medical history).
Ensure the confidentiality of clinical trial participants and sponsors is respected.
May confirm participant statuses or results.
Ensure timely communication of any issues/questions to the appropriate department throughout participation in studies.
Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
Identify recurring eligibility challenges or frequently asked questions and provide feedback to the team.