Clinical Research Coordinator

The Clinical Research Coordinator (CRC) is responsible for the day-to-day operational management of clinical research studies conducted at Salma Health. Working under the supervision of the Clinical Research management team, the CRC ensures that all research activities are conducted in compliance with federal regulations, institutional policies, and Good Clinical Practice (GCP) guidelines. This role serves as the primary point of contact for study sponsors, IRB submissions, and research participants. The role requires working 5 days a week in person in our La Jolla clinic.

Key Responsibilities:

Study Management & Operations

• Coordinate all operational aspects of assigned clinical trials from startup through closeout
• Assist in the development and review of study protocols, amendments, and informed consent documents
• Maintain and organize study files, regulatory binders, and essential documents per ICH/GCP guidelines
• Prepare and submit IRB applications, continuing reviews, amendments, and adverse event reports
  
  

Participant Coordination

• Recruit, screen, and schedule study participants in accordance with protocol eligibility criteria
• Conduct study visits, collect data, and perform protocol-specified assessments (e.g., vital signs, EEGs, sample collection) per training and delegation
• Maintain ongoing communication with participants to support retention and protocol adherence
  
  

Data Management

• Enter and verify data in electronic data capture (EDC) systems (e.g., REDCap, Medidata Rave) with accuracy and timeliness
  
  

Regulatory & Compliance

• Ensure all study activities comply with FDA regulations (21 CFR Parts 50, 54, 56, 312, 812), ICH E6 GCP, and institutional SOPs
• Facilitate and support sponsor monitoring visits, internal audits, and regulatory inspections
  
  

Collaboration & Communication

• Serve as the primary liaison between study sponsors, CROs, the IRB, and clinical departments
• Communicate study status, enrollment updates, and issues to the PI and research management team
• Mentor and provide guidance to junior research staff or volunteers as needed
  
  

Required Qualifications:

• Bachelor's degree in a health science, life science, nursing, or related field
• Minimum 2 years of clinical research with experience running Phase I-III clinical trials or equivalent combination of education and experience
• Working knowledge of FDA regulations, GCP guidelines, and IRB processes
• Proficiency with electronic data capture systems and Microsoft Office Suite
• Strong organizational skills with meticulous attention to detail
• Excellent written and verbal communication skills
• Ability to manage multiple priorities in a fast-paced research environment
  
  

Preferred Qualifications:

• Familiarity with REDCap, Medidata Rave, or similar EDC platforms
• Bilingual or multilingual skills are a plus
  
  

Compensation & Benefits

The compensation for this position includes:

• Base: $72,000- $90,000 (depending on experience & qualifications)
• Benefits: Medical, dental, vision, PTO, and additional benefits
  
  

We reserve the right to modify benefit offerings at any time, in accordance with applicable laws.

Compensation Range: $72K - $90K