Remote Senior CRA — Sponsor-Focused Trials

Syneos Health, Inc.

Nevada (IA)

Hybrid

USD 70,000 - 100,000

Full time

14 days+

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Benefits offered by this job

Company car or car allowance
Health benefits
401k match
Stock purchase plan

Job summary

Syneos Health is seeking an Experienced Clinical Research Associate for sponsor-dedicated monitoring. The role emphasizes remote work with travel up to 75% across sites, ensuring regulatory and protocol compliance, data integrity, and site management throughout the study lifecycle.

The candidate should have a Bachelor’s degree or RN, knowledge of ICH-GCP, and strong communication skills to collaborate with site staff and project teams.

Qualifications

  • Bachelor’s degree or RN in a related field or equivalent
  • Knowledge of Good Clinical Practice/ICH Guidelines
  • Excellent communication and interpersonal skills
  • Willingness to travel up to 75% regularly
  • Ability to use computer systems and data tools

Responsibilities

  • Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (on-site or remotely) ensuring regulatory, ICH-GCP and/or GPP and protocol compliance.
  • Verifies informed consent procedures and protects subject confidentiality; assesses safety and data integrity factors at investigator sites.
  • Assesses site processes, conducts source document review, verifies CRF data accuracy, and manages query resolution.
  • Manages IP inventory, storage, and labeling per protocol; ensures proper release/return.
  • Reviews ISF for accuracy and reconciles with TMF; ensures archiving per guidelines.

Skills

Communication skills
Computer skills
Willingness to travel
Interpersonal skills

Education

Bachelor’s degree or RN

Job description

Syneos Health is seeking an Experienced Clinical Research Associate for sponsor-dedicated monitoring. The role emphasizes remote work with travel up to 75% across sites, ensuring regulatory and protocol compliance, data integrity, and site management throughout the study lifecycle.

The candidate should have a Bachelor’s degree or RN, knowledge of ICH-GCP, and strong communication skills to collaborate with site staff and project teams.

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