Clinical Research Associate — Remote & Field Monitoring

Syneos Health, Inc.; Colorado; Remote; USD 70,000 - 95,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (Medical, Dental, Vis)

401k match

Employee Stock Purchase Plan

Bonuses/commissions

Paid time off (PTO)

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate to be regionally aligned across the US. You will monitor sites, ensure GCP compliance, manage data quality and site relationships throughout the study lifecycle.

Join a collaborative team that values patient-centric trials, rigorous training, and a range of benefits. This role requires travel up to 75% and strong communication skills to coordinate with sponsors, sites and internal teams.

Qualifications

• Bachelor’s degree or RN in a related field or equivalent.
• Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements.
• Excellent communication, presentation and interpersonal skills.
• Ability to travel up to 75% on a regular basis.

Responsibilities

• Performs site qualification, initiation, monitoring and close-out visits (on-site or remote) with GCP and protocol compliance.
• Verifies informed consent, protects confidentiality and assesses subject safety and data integrity.
• Conducts source data review, manages query resolution and ensures ISF/TMF accuracy.
• Manages IP inventory and release in accordance with protocol and regulations.
• Supports site training, recruitment and data tracking throughout the study lifecycle.
• Communicates with sponsor and site teams to meet timelines and deliverables.
• Attends investigator meetings and audit-prep activities as required.

Skills

Computer skills

Communication skills

Interpersonal skills

Travel up to 75%

Education

Bachelor's degree or RN in related field

Job description

Syneos Health is seeking an Experienced Clinical Research Associate to be regionally aligned across the US. You will monitor sites, ensure GCP compliance, manage data quality and site relationships throughout the study lifecycle.

Join a collaborative team that values patient-centric trials, rigorous training, and a range of benefits. This role requires travel up to 75% and strong communication skills to coordinate with sponsors, sites and internal teams.