Join Us at Centricity Research!
Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.
About the Role
We’re looking for a Clinical Screening Coordinator to lead research-related recruitment initiatives and ensure the enrollment of high-quality patients in accordance with Centricity Research recruitment guidelines. In this role, you’ll also screen patients for participation in clinical research studies with a solid understanding of study protocols, including inclusion/exclusion criteria, relevant medications, and medical conditions.
This is a fully on-site role. In addition to the hourly rate, this role is eligible for incentive compensation.
What You’ll Do
- Work on enrollment and retention initiatives with the Site Manager
- Problem solve and create contingency plans to optimize enrollment via recruitment initiatives
- Obtain and maintain computerized database of all ad callers
- Return all phone calls/email responses to interested patients within 24 - 48 hours
- Accurately complete recruitment tracking log and all applicable clinical trial management systems
- Identify appropriate study candidacy based on knowledge of sites’ recruiting and upcoming studies
- Complete database query reviews for study candidacy and conduct outbound calls for study interest
- Provide study metrics on a regular basis and provide ongoing feedback regarding outcome of recruitment initiatives
- Occasionally attend community lectures, health fairs or events to promote Centricity Research
- Promote clinical trials in the community through outreach events
- Complete Informed Consent and screening visits per study protocol and Centricity Research SOP
- Perform delegated tasks completely and accurately, including review of demographic information, medication history, medical history, obtaining vital signs (blood pressure, heart rate, temperature, and waist, weight, and height measurements
- Complete the source documents, case report forms, and data queries in a timely manner, accurately, and completely.
- Assist the Central Recruitment, Research Operations and/or Investigators with any other tasks as required
- Able to work in a regional setting to support sites with recruitment and screening as needed
You Might Be a Great Fit If You:
- Communicate clearly and comfortably with patients by phone, email, and in person
- Stay organized and pay attention to details, especially when managing multiple tasks like outreach, documentation, and scheduling
- Are curious about clinical research and excited to learn protocols, medical terminology, and research ethics
- Feel confident using everyday computer tools like spreadsheets, databases, and email, and are open to learning systems like CTMS or EMR
- Bring experience from a healthcare, research, or customer-facing role, or are ready to dive in and learn on the job
Why Centricity Research?
Our Mission
We connect people to scientific advancements through groundbreaking research within a deeply human experience.
Our Core Values
- Quality: We aim for excellence and integrity in everything we do - because lives depend on it.
- Care: We show up for each other, our customers, and our mission - always going the extra mile.
- Be the Change You Seek: We're adaptable, forward-thinking, and constantly improving - for the betterment of all.
- One Team: We collaborate, support one another, and succeed together.
- Grow for Good: We grow with purpose - to expand access to research and improve global health.
- Own It: We take initiative, deliver results, and follow through - with passion and accountability.
Benefits
- Comprehensive health, dental, and vision insurance
- Enhanced EAP – mental health support
- Flexible PTO + paid holidays
- Continuing education reimbursement
- 401(k) / RRSP with company match and immediate vesting
Ready to Apply?
We’d love to hear from you – apply now!
We’re an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applicants from all backgrounds and will provide accommodations during the hiring process upon request.
The pay range for this role is:
21.00 - 23.00 USD per hour (Centricity Research Rincon Pulmonology)
Skills Required
- Work fully on-site at the research site
- Complete informed consent and screening visits per study protocol and SOPs
- Perform delegated clinical tasks (review demographics, med history, obtain vital signs, measure weight/height/waist)
- Knowledge of study protocols including inclusion/exclusion criteria, medications, and medical conditions
- Respond to patient phone calls/emails within 24-48 hours and maintain recruitment tracking logs
- Proficiency with everyday computer tools (spreadsheets, databases, email) and willingness to learn CTMS and EMR
- Strong communication, organizational skills, and attention to detail
- Experience in healthcare, research, or customer-facing roles, or willingness to learn on the job
- Ability to support regional sites and occasionally attend community outreach events
What We Do
Centricity Research is an integrated research organization (IRO) with more than 40 wholly owned and integrated clinical research offices across North America. The company conducts Phase I-IV clinical research in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials. For more than 25 years, the organization’s founders have worked to revolutionize research by investing in the people and technology needed to deliver outstanding clinical trial experiences, earning numerous awards including “Best Places to Work” and recognition for “Outstanding Diversity in Clinical Research.” Jobseekers: Apply here >> https://centricityresearch.applytojob.com/apply
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