Title: Clinical Research Coordinator 3
Work Location: Sioux Falls, South Dakota 57104
Assignment Duration: 5+ Months
Part Time, 8 hours per day; prefer Monday, Tuesday, Friday.

**The clinical site has requested a CRC that is seasoned in their skillset with all aspects of coordinating trials and be able to articulate their experience and exactly what they've done onsite in this role. The site manager will ask specific questions during the interview process to determine their level of understanding with the CRC role and industry standards

Additional Skills/Qualifications:

• Focus on recruitment and pre-ICF activities:
• Pre-screening & recruitment support including chart reviews, referral management and community outreach
• Make eCRF entries, corrections and queries
• Investigator Site File maintenance
• Regulatory experience would be a plus

Description:

Summary

• Perform clinical procedures to collect, record, and interpret patient data for clinical studies

• Follow study protocols, SOPs, and Good Clinical Practice (GCP) guidelines

• Assist with daily workload planning and coordination

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Key Responsibilities

Study Preparation & Support

• Review study protocols, Case Report Forms (CRFs), and study-related documents

• Work with electronic data capture systems

• Attend study-related meetings

• Support investigators in executing research studies

Regulatory & Compliance

• Collect and submit regulatory/ethics documents (FDA and other bodies)

• Ensure compliance with protocols, SOPs, and clinical research standards

• Prepare for audits, monitoring visits, and regulatory inspections

Patient Interaction & Recruitment

• Recruit, screen, and enroll patients for clinical trials

• Maintain subject screening logs

• Educate patients about study purpose, procedures, and timelines

• Address patient queries and provide ongoing support

Study Execution

• Schedule and conduct study visits

• Perform clinical procedures (ECG, spirometry, vital signs, sample collection, etc.)

• Handle lab work including specimen preparation and logistics

• Monitor patient safety and report adverse events

Data Management & Quality

• Collect, record, and maintain accurate study data

• Ensure data quality, accuracy, and completeness

• Assist with data review, query resolution, and database development

Collaboration & Coordination

• Participate in daily team “huddles” for task planning

• Coordinate with team members to ensure smooth study execution

• Assist with staffing and scheduling for research projects

Training & Support

• Train new staff on study-specific requirements

• Maintain and audit training records

• Support adherence to training and compliance standards

Study Oversight

• Assist investigators in meeting study timelines, budgets, and objectives

• Ensure adherence to regulatory and quality standards

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? Required Knowledge, Skills & Abilities

• Strong knowledge of clinical trials and medical terminology

• Familiarity with protocols, SOPs, consent forms, and study schedules

• Proficiency in MS Office (Excel, Word, Outlook, Access)

• Excellent interpersonal and communication skills

• Strong attention to detail

• Ability to build and maintain professional relationships

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? Education & Experience

• High school diploma required (Bachelor’s degree preferred)

• Relevant experience in a clinical or medical setting

• Equivalent combination of education, training, and experience acceptable

• Required certifications/licenses as per company or regulatory standards

 
 
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 30.00/hr.