Participant Recruitment Agent
Altasciences
Participant Recruitment Agent
Altasciences
Integrated CRO for early-phase drug development
About The Role
The Participant Recruitment Agent will provide volunteers with preliminary clinical trial information and company details as well as pre-screen volunteers to determine eligibility for clinical trial screening. The Participant Recruitment Agent will ensure all tasks performed are executed in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.
What You'll Do Here
Ensure the confidentiality of clinical trial participants and sponsors is respected.
Maintain and advocate a high level of customer service and quality within the department.
Review and understand all assigned actively enrolling studies.
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.
Schedule screening and/or other clinical trial related appointments.
Update participant management software with volunteer demographics and medical history.
May confirm participant statuses and prepare/send check-in lists for clinical operations teams.
Strive to achieve study recruitment targets and departmental objectives.
Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
What You'll Need to Succeed
High School Diploma or GED required; college degree and related work experience preferred.
Good Communication
Customer service focused
Able to work in fast-paced environment
What We Offer
This is a variable hour position. The estimated hourly rate for this position is $19.00 - $23.00. Please note that salaries vary within the range based on factors including, but not limited to, prior relevant experience, skills, education, certification, location as well as internal equity and market data.
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Integrated CRO for early-phase drug development
Altasciences provides integrated early-stage drug development services, covering preclinical testing, early clinical trials, and contract manufacturing. It functions as a single, in-house CRO that coordinates discovery support, safety testing, clinical research, and manufacturing to streamline a program from start to early proof of concept. The company differentiates itself by offering an end-to-end, one-stop path rather than requiring clients to contract multiple vendors. Its goal is to help innovator programs move quickly and efficiently through early development to speed up decision making and progression to later-stage trials.
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