# Clinical Research Coordinator II

**Company**: Syneos Health
**Location**: Miami, FL
**Work arrangement**: onsite
**Experience**: mid
**Job type**: full-time
**Salary**: $base salary range not specified, but actual salary will vary based on various factors
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-FL-Miami/Clinical-Research-Coordinator-II---Miami--FL--Future-Opportunities-_25112601?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_04a32d01-216

## Description

Clinical Research Coordinator II - Miami, FL (Future Opportunities)

Syneos Health is seeking a Clinical Research Coordinator II to support a clinical trial in Miami, FL. The successful candidate will be responsible for coordinating and performing various study-related activities, including protocol preparation, study conduct, and post-clinic/close-out activities.

**Job Responsibilities**

- Review and prepare study protocols, informed consent forms, and other study-related documents

- Coordinate study start-up activities, including clinic logistics planning and team training

- Manage multiple clinical trials simultaneously and prioritize tasks effectively

- Collect and enter study data into the appropriate system

- Develop patient rapport and explain research protocols to minimize protocol violations

- Coordinate and monitor screening activities and provide support as required

- Assist with informed consent of study subjects

- Submit data in required timeframe and complete Case Report Forms

- Facilitate audits of study data and respond to inquiries by auditors

- Take the lead and/or overall coordination of clinic activities, including supervising clinic visits and screening eligibility prior to randomization

- Coordinate resolution and/or address QC, monitor, CRF, or other internal/external findings

- Review and/or oversee close-out of study documentation and deviation reporting

**Qualification Requirements**

- Registered Nurse and/or University Degree such as Bachelor of Science Degree required

- Clinical Research certification preferred

- A minimum of 1 year experience in clinical research required, preferably in coordination of clinical research projects

- Good knowledge of regulations, ICH GCP, privacy, and applicable guidelines

- Required skills: problem solving, planning, and evaluation

- Possess good time management, detail-oriented, and able to multi-task

- Good interpersonal and communication skills with a team focus

- Knowledge of SOP writing and ability to anticipate problems and provide solutions in a timely manner

- Ability to coordinate multiple clinical research projects with competing deadlines

- Proficiency in computer software programs (e.g. Word, Excel, Power Point)

- Proficiency in use of various clinical trial EDC software preferred

**Benefits**

- Company car or car allowance

- Health benefits, including Medical, Dental, and Vision

- Company match 401k

- Eligibility to participate in Employee Stock Purchase Plan

- Eligibility to earn commissions/bonus based on company and individual performance

- Flexible paid time off (PTO) and sick time

## Skills

### Required
- clinical research
- protocol preparation
- study conduct
- data entry
- patient rapport
- regulatory guidelines
- SOP writing
- problem solving
- planning
- evaluation
- time management
- detail-oriented
- multi-tasking
- interpersonal skills
- communication skills
- team focus

### Nice to have
- Clinical Research certification
- EDC software

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-FL-Miami/Clinical-Research-Coordinator-II---Miami--FL--Future-Opportunities-_25112601?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)