Remote Clinical Research Monitor

Syneos Health, Inc.; Indianapolis (IN); Remote; USD 65,000 - 90,000; Full time

Benefits offered by this job

Company car or car allowance

Health benefits (medical, dental, and视

401k match

Employee Stock Purchase Plan

Paid time off

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate (CRA) regionally aligned across the United States. You will monitor sites, ensure ICH-GCP compliance, manage data quality and site communications, and support life-cycle activities from initiation to close-out.

The role requires travel up to 75% and ability to work remotely within the US. You will collaborate with cross-functional teams to accelerate trials and improve patient outcomes, contributing to our global development

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
• Excellent communication, presentation and interpersonal skills
• Ability to manage required travel of up to 75% on a regular basis
• US ONLY: As part of your employment with Syneos Health, you may be deployed to Sites that require certain medical and other personal information to gain facility access. Pursuant to our Employee Privacy Notice, Syneos Health can provide the Sites with the information necessary for you to gain such access. Further, a Site may ask you for additional information beyond that which Syneos Health has in its possession. You are required to comply with any such Site requests as a condition of your employment with Syneos Health. Please note that failure to provide requested information may result in a Site barring you from entry, which could put your ongoing employment at risk.

Responsibilities

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.
• Verifies the process of obtaining informed consent and protects confidentiality; assesses safety and data integrity at investigator sites.
• Per the CMP/SMP: assesses site processes, conducts source data review, verifies CRF data, and drives query resolution to closure.
• May perform IP inventory, labeling, storage, and release/retrieval per protocol.
• Routinely reviews ISF for accuracy, reconciles with TMF, and ensures archiving of essential documents.
• Documents activities and supports recruitment, retention and data tracking.
• Manages site-level activities, budgets, timelines, and communications; adapts to changing priorities.
• Attends Investigator Meetings and sponsor meetings; supports audit readiness and training.

Skills

Excellent communication skills

Good computer skills

Ability to travel up to 75%

Knowledge of GCP/ICH Guidelines

Education

Bachelor's degree or RN in related field

Job description

Syneos Health is seeking an Experienced Clinical Research Associate (CRA) regionally aligned across the United States. You will monitor sites, ensure ICH-GCP compliance, manage data quality and site communications, and support life-cycle activities from initiation to close-out.

The role requires travel up to 75% and ability to work remotely within the US. You will collaborate with cross-functional teams to accelerate trials and improve patient outcomes, contributing to our global development