ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with an expertise in early and late-stage neuroscience drug development. With 21 wholly owned clinical sites and 5 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 340+ in-patient beds, a large and growing database of patients suffering from mental illness, neurological disorders, sleep disorders, addictions, Acute and Chronic Pain, diabetes, and other illnesses.

Why join us?

CPMI is a reputable, collaborative, Phase I clinical trial site that will guide you in your career. ERG, CPMI’s parent company, offers career development and encourages employees to achieve their goals. We offer a competitive salary based on experience and a range of benefits including medical, dental, vision, 401k, and PTO.

Job Responsibilities:

• Administration of study drugs as required by the specific protocol
• Ensures all study procedures are conduct as required by specific protocol (i.e., vital signs, draw blood, sample processing, sample shipping, etc.)
• Maintains safety and well-being of study participants during assigned shift

• Performs venipuncture, vital signs (including blood pressure, pulse, temperature, respiration), ECG, weight, height
• Confer with patient to obtain information for laboratory records and explain procedures

• Verifies that the appropriate vials and containers necessary for specimen collection
• Ensure study data is collected following plan of care, guidelines and identified group resources
• Evaluate clinical practice and review clinical records to ensure standards of care and quality of services are provided in accordance with SOPs

Additional Responsibilities:

• Demonstrates a caring, professional attitude and behavior toward study participants and staff, actively contributing to the well-being and dignity of the clinic
• Maintains an overall good work attitude, promoting cooperation and professionalism and interactions with other staff members

Skills and Qualifications:

• Education and experience

• A minimum of a high school diploma with 3 years research experience OR Licensure/ Certifications in a clinical or health field with a minimum of one-year clinical research experience
• BLS and/or ACLS, phlebotomy and injection certifications preferred

• Requirements
  • Understands regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
  • Knowledgeable in medical terminology
  • Excellent communication skills (interpersonal, written, verbal) and basic computer skills