Senior Clinical Research Associate – Remote/On‑Site

Syneos Health/ inVentiv Health Commercial LLC; Billings (MT); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (Medical, Dental, and

401k with company match

Employee Stock Purchase Plan

Bonus based on company and individual绩

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate (Sponsor Dedicated) to join our global Clinical Development team. This role involves site qualification, initiation, monitoring, data review and close-out visits, with potential on-site or remote work and significant travel to trial sites.

Qualified candidates hold a Bachelor's degree or RN, knowledge of GCP/ICH guidelines, and strong communication skills; travel up to 75% is expected as part of site management across studies

Qualifications

• Bachelor's degree or RN in a related field is required or equivalent experience.
• 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 remotely) ensuring ICH-GCP and protocol compliance.
• Verifies informed consent and protects subject confidentiality, assessing safety and data integrity.
• Reviews ISF/TMF, conducts data review, and guides site staff to timely query resolution.
• Manages IP inventory, labeling, and storage per protocol and regulatory requirements.
• Ensures site training, audits readiness, and supports recruitment and retention activities.

Skills

GCP/ICH knowledge

Excellent communication skills

Presentation skills

Interpersonal skills

Travel readiness up to 75%

Computer skills

Education

Bachelor's degree or RN in a related field or equivalent

Job description

Syneos Health is seeking an Experienced Clinical Research Associate (Sponsor Dedicated) to join our global Clinical Development team. This role involves site qualification, initiation, monitoring, data review and close-out visits, with potential on-site or remote work and significant travel to trial sites.

Qualified candidates hold a Bachelor's degree or RN, knowledge of GCP/ICH guidelines, and strong communication skills; travel up to 75% is expected as part of site management across studies