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Full-time

Clinical Research Coordinator - On-Site

Competitive

Bountiful, UTScience & PharmaceuticalPosted 18d ago

You'll complete your application on the employer's website.

Role overview

Job type

Full-time

Salary

Competitive

Posted

18 days ago

Job description

Seacrest Behavioral Health is hiring an on-site Clinical Research Coordinator to manage multiple clinical trials and oversee study activities. The role includes conducting clinical procedures, coordinating trials from initiation through completion, supporting audits, and mentoring junior staff.

Responsibilities

Managing 2-6 concurrent trials across different therapeutic areas

Patient recruitment, obtaining informed consent, and handling regulatory documentation

Performing clinical procedures such as vital signs, phlebotomy, and ECGs

Coordinating study activities from initiation to completion and during site audits

Mentoring junior staff and supporting internal training initiatives

Company

National substance use disorder and mental health treatment program

Delray Beach, Florida, USA

https://www.seacrestrecoverycenter.com/

Founded in 2015

51-200 employees

Qualifications

1-3 years of clinical research experience at an investigative site (CRC I level) or more for CRC II

Proficiency in vital signs, phlebotomy, ECGs, and specimen processing

Excellent written and verbal communication with strong attention to detail

Understanding of site operations and drug development processes

Competency with CTMS, eCRF systems, and Microsoft Office

Seacrest Recovery Center is a National Substance Use Disorder and Mental Health Treatment Program.

Delray Beach, Florida, USA

https://www.seacrestrecoverycenter.com

Growth Stage

Leadership Team

Josh Fenster

Co-Founder and CEO

Jared Pruzan

Co-Founder / CFO

Company data provided by

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Required skills

Clinical Research, Vital Signs, Phlebotomy, ECG, Specimen Processing, Drug Development, Microsoft Office

Preferred skills

Written and Verbal Communication

Experience

1-3 years

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