Medix™
Overview
Bilingual Clinical Research Recruiter - 247138 This range is provided by Medix™. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$18.00/hr - $22.00/hr Direct message the job poster from Medix™ Are you a highly motivated, detail-oriented professional with exceptional people skills and a passion for connecting people with clinical breakthroughs? The primary mission of this role is to drive the success of clinical trials by
ethically recruiting a diverse pool of qualified participants . You will be the crucial first point of contact, managing the participant pipeline from initial outreach through final eligibility screening, all while ensuring strict adherence to study protocols and regulatory standards.
Responsibilities
Participant Recruitment and Screening
Proactive Outreach:
Place a high volume of daily
outbound calls
and actively engage with the community at health fairs and outreach events to promote clinical research and attract potential volunteers.
Comprehensive Screening:
Conduct thorough
phone and in-person interviews
and pre-screens to assess a volunteer's interest, willingness to commit, and initial eligibility for multiple research studies.
Eligibility Determination:
Master and apply the specific
inclusion and exclusion criteria
for each clinical protocol. Review pertinent
past medical history, current medications, and medical conditions
to accurately determine a volunteer's eligibility.
Clinical Collaboration:
Coordinate with study doctors and study coordinators as needed to review a subject's history and confirm eligibility.
Data Management:
Accurately
review, enter, and edit subject information
in the clinical research management system software.
Confidentiality:
Strictly maintain the
confidentiality
of all participant information.
Team Support and Administration
Enrollment Support:
Assist the Clinical Team with in-person pre-screening, foster strong
customer relations
with volunteers, and support
sponsor relations
regarding enrollment efforts.
Strategic Planning:
Participate in team meetings and training, providing regular
reports on potential eligibility
and contributing to strategic
recruitment planning
for upcoming studies.
Communication:
Maintain regular and effective communication with the supervisor/coordinator regarding any issues or challenges.
Office Duties:
Perform other related administrative and office duties as assigned.
Qualifications and Requirements Education & Experience
Required:
High School Diploma.
Preferred:
Associate's degree; a medical background or familiarity with
medical terminology .
Bilingual Requirement:
Fluency in both Spanish and English is required
to effectively serve our diverse community and clinical trial needs.
Tech Savvy:
Familiarity with or the proven
ability to quickly learn
clinical trial management system software.
Exceptional Communication:
Excellent
people skills
and a high comfort level with making a large volume of outbound calls daily.
Organizational Excellence:
Highly
detail- and multi-task oriented
with strong time management skills.
Technical Proficiency:
Excellent
computer and data entry skills .
Independence:
Proven
ability to work independently
and manage a dynamic workload.
Physical Requirements The role requires the ability to sit, stand, walk, reach, and use hands and fingers for extended periods. Must be able to occasionally lift and/or move up to
25 pounds .
Seniority level
Not Applicable
Employment type
Full-time
Job function
Research
Industries
Research Services
#J-18808-Ljbffr
Bilingual Clinical Research Recruiter - 247138 This range is provided by Medix™. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$18.00/hr - $22.00/hr Direct message the job poster from Medix™ Are you a highly motivated, detail-oriented professional with exceptional people skills and a passion for connecting people with clinical breakthroughs? The primary mission of this role is to drive the success of clinical trials by
ethically recruiting a diverse pool of qualified participants . You will be the crucial first point of contact, managing the participant pipeline from initial outreach through final eligibility screening, all while ensuring strict adherence to study protocols and regulatory standards.
Responsibilities
Participant Recruitment and Screening
Proactive Outreach:
Place a high volume of daily
outbound calls
and actively engage with the community at health fairs and outreach events to promote clinical research and attract potential volunteers.
Comprehensive Screening:
Conduct thorough
phone and in-person interviews
and pre-screens to assess a volunteer's interest, willingness to commit, and initial eligibility for multiple research studies.
Eligibility Determination:
Master and apply the specific
inclusion and exclusion criteria
for each clinical protocol. Review pertinent
past medical history, current medications, and medical conditions
to accurately determine a volunteer's eligibility.
Clinical Collaboration:
Coordinate with study doctors and study coordinators as needed to review a subject's history and confirm eligibility.
Data Management:
Accurately
review, enter, and edit subject information
in the clinical research management system software.
Confidentiality:
Strictly maintain the
confidentiality
of all participant information.
Team Support and Administration
Enrollment Support:
Assist the Clinical Team with in-person pre-screening, foster strong
customer relations
with volunteers, and support
sponsor relations
regarding enrollment efforts.
Strategic Planning:
Participate in team meetings and training, providing regular
reports on potential eligibility
and contributing to strategic
recruitment planning
for upcoming studies.
Communication:
Maintain regular and effective communication with the supervisor/coordinator regarding any issues or challenges.
Office Duties:
Perform other related administrative and office duties as assigned.
Qualifications and Requirements Education & Experience
Required:
High School Diploma.
Preferred:
Associate's degree; a medical background or familiarity with
medical terminology .
Bilingual Requirement:
Fluency in both Spanish and English is required
to effectively serve our diverse community and clinical trial needs.
Tech Savvy:
Familiarity with or the proven
ability to quickly learn
clinical trial management system software.
Exceptional Communication:
Excellent
people skills
and a high comfort level with making a large volume of outbound calls daily.
Organizational Excellence:
Highly
detail- and multi-task oriented
with strong time management skills.
Technical Proficiency:
Excellent
computer and data entry skills .
Independence:
Proven
ability to work independently
and manage a dynamic workload.
Physical Requirements The role requires the ability to sit, stand, walk, reach, and use hands and fingers for extended periods. Must be able to occasionally lift and/or move up to
25 pounds .
Seniority level
Not Applicable
Employment type
Full-time
Job function
Research
Industries
Research Services
#J-18808-Ljbffr