Senior Clinical Research Associate — Remote Sponsor

Syneos Health, Inc.; Pennsylvania; Hybrid; USD 80,000 - 110,000; Full time

Benefits offered by this job

Company car/allowance

Health benefits (medical, dental, VIs)

401k

Employee stock purchase plan

Bonuses

Paid time off

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate for sponsor-dedicated monitoring. This remote role includes site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance and patient safety.

You will review ISF/TMF, support recruitment, and coordinate with site staff to drive data integrity and regulatory adherence. Required are a Bachelor’s degree or RN, strong knowledge of GCP/ICH, excellent communication and interpersonal skills, and the

Qualifications

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Must demonstrate good computer skills and be able to embrace new technologies.

Responsibilities

• Performs site qualification/initiation/monitoring and close-out visits, on-site or remote, ensuring protocol compliance.
• Verifies informed consent processes and protects subject confidentiality; assesses safety and data integrity factors.
• Conducts site/source data review, data entry checks, and supports query resolution to closure.
• Manages IP inventory, labeling, and compliance with protocol for dispensed/returned IP.
• Reconciles ISF and TMF; ensures archiving of essential documents per regulations.
• Participates in meetings, supports recruitment, tracking, and action item resolution.

Skills

Communication skills

Presentation skills

Interpersonal skills

Travel up to 75%

GCP/ICH knowledge

Computer skills

Education

Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience

Job description

Syneos Health is seeking an Experienced Clinical Research Associate for sponsor-dedicated monitoring. This remote role includes site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance and patient safety.

You will review ISF/TMF, support recruitment, and coordinate with site staff to drive data integrity and regulatory adherence. Required are a Bachelor’s degree or RN, strong knowledge of GCP/ICH, excellent communication and interpersonal skills, and the