Regional Clinical Research Associate - Remote Options

Syneos Health, Inc.; Oklahoma; On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Company car / car allowance

Health benefits (medical, dental, and视

401k with company match

Employee stock purchase plan

Bonus program

Paid time off (PTO)

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to support regionally across the US. The role involves site qualification, monitoring, data verification, and coordination with investigators to ensure GCP compliance and study timelines.

You'll travel up to 75% across the US, work with cross-functional teams, and contribute to the successful delivery of clinical trials while upholding patient safety and data integrity.

Qualifications

• Knowledge of Good Clinical Practice/ICH guidelines and regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Ability to manage travel up to 75% on a regular basis.

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or GPP and protocol compliance.
• Verifies the process of obtaining informed consent and safeguards confidentiality; assesses factors affecting patient safety and data integrity.
• Per CMP/SMP: assesses site processes; conducts Source Document Review and data verification; manages query resolution and ISF/TMF alignment.
• May handle IP inventory, storage, labeling, and release per protocol; ensures regulatory compliance.
• Prepares for Investigator Meetings; participates in global project meetings and training; supports audits.

Skills

Excellent communication skills

Ability to travel up to 75%

Regulatory/GCP knowledge

Team collaboration

Education

Bachelor's degree or RN in a related field

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to support regionally across the US. The role involves site qualification, monitoring, data verification, and coordination with investigators to ensure GCP compliance and study timelines.

You'll travel up to 75% across the US, work with cross-functional teams, and contribute to the successful delivery of clinical trials while upholding patient safety and data integrity.