Clinical Trial Recruitment Representative

Clinical Trial Recruitment Representative - On-Site - US, Lenexa, KS

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are currently seeking a Clinical Trial Recruitment Representative to join our diverse and dynamic team. As a Clinical Trial Recruitment Representative at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Overview of the role:

Title: Clinical Trial Recruitment Representative

Location: On-Site (Lenexa, KS)

Job Type: Full-Time

General Summary

Ensure consistent and accurate processing of subject registration in the volunteer database and all necessary actions prior to entry to the screening process. Recruits study subjects for clinical trials by conducting phone screens and scheduling screening appointments.

Primary Responsibilities: 

• Answers and places phone calls with potential study subjects to determine initial study eligibility requirements. Explains study protocols to volunteers for each study during phone screening.

• Maintains accuracy of recruiting database and performs database queries.

• Responsible for accurate processing of subject registration in the volunteer database and collects all necessary documents
  needed prior to subject entry to the screening process.

• Responsible for actioning all voice mail messages from study volunteers.

• Works as a member of the recruiting team to obtain sufficient numbers of qualified volunteers for each study.

Additional Responsibilities: 

• Makes confirmation calls for screening appointments and volunteer check-in dates.

• Notifies study volunteers of study participation status and responds to volunteer questions and comments.

• Checks in study volunteers for screening appointments and may plan follow-up visits or screening appointments.

• Assists with training and mentoring more junior team members.

• Coordinates necessary payments to volunteers and may maintain referral program.

Qualifications: 

• High school diploma

• 2 years of relevant experience

• Past customer service experience preferred

• Working knowledge of the drug development process

• Working knowledge of medical terminology

• Good written and oral communication skills

• Basic ability to read and interpret study protocols

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements

• A range of health insurance offerings to suit you and your family’s needs.

• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.

• Life assurance

• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundament