# Research Assistant

**Company**: IQVIA
**Location**: Flint, MI
**Work arrangement**: onsite
**Job type**: part-time
**Salary**: $25.00-$39.00 per hour
**Category**: Research
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Flint-MI/Site-Research-Assistant---Flint--MI_R1575477?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_b0cef018-9cc

## Description

We are seeking a Research Assistant (RA) to join our team in Flint, MI, and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance. The potential base pay range for this role is $25.00-$39.00 per hour.

**Key Responsibilities:**

- Perform accurate EDC data entry, manage queries, and ensure timely resolution.

- Maintain and update the regulatory binder in compliance with documentation and audit standards.

- Coordinate and schedule subject visits, procedures, and follow-up activities.

- Build effective working relationships with investigators, clinical staff, and study team members.

- Support subject screening, recruitment, and enrollment activities.

- Assist with patient/research participant scheduling and collection of medical history.

- Coordinate lab procedures and follow-up care in alignment with study protocols.

- Ensure strict adherence to IRB‑approved protocols, including assistance with informed consent processes.

- Uphold participant safety and report concerns promptly per SOPs and Sponsor requirements.

- Follow all company policies, SOPs, guidelines, and Good Clinical Practice (GCP) standards.

**Qualifications:**

- Associate degree preferred or equivalent combination of education and relevant experience.

- 1+ years of experience in a clinical research environment preferred.

- Strong working knowledge of clinical trials, GCP, and protocol‑specific procedures.

- Proficiency with EDC systems, data entry accuracy, and query management.

- Experience with visit scheduling, regulatory documentation, and binder maintenance.

- Excellent attention to detail, time management, and task prioritization.

- Strong communication, interpersonal, and relationship‑building skills.

**Benefits:**

- The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

## Skills

### Required
- EDC systems
- data entry
- query management
- clinical trials
- GCP
- protocol‑specific procedures
- visit scheduling
- regulatory documentation
- binder maintenance
- time management
- task prioritization
- communication
- interpersonal skills
- relationship‑building skills

### Nice to have
- associate degree
- 1+ years of experience in a clinical research environment
- proficiency with EDC systems

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Flint-MI/Site-Research-Assistant---Flint--MI_R1575477?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)