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CRA II at Syneos Health - ApplyBlast

CRA II

Syneos Health

4 months ago

China

Hybrid

Full Time

Senior

0 applicants

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About this role

A Clinical Research Associate II at Syneos Health performs site qualification, monitoring, and management activities in compliance ICH-GCP guidelines to ensure data integrity and regulatory adherence. The role involves verifying informed consent processes, reviewing source documents, managing investigational product inventory, and supporting study recruitment and audit readiness. CSR II must engage directly with investigators and site staff, often requiring significant travel, to drive clinical study objectives and ensure participant safety.

Responsibilities

Perform site qualification and initiation visits ensuring regulatory compliance
Conduct source document reviews and verify clinical data accuracy
Manage investigational product inventory and storage security
Support subject recruitment and retention strategies
Prepare sites for audit readiness and respond to findings

Skills

Qualifications

Bachelor's degree in a related fieldRegistered Nurse (RN)

About Syneos Health

syneoshealth.com

Headquarters

Morrisville, North Carolina, United States

Company Size

10001+ employees

Founded

2017

View Profile

Syneos Health is a biopharma solutions organization and full‑service contract research organization (CRO) that integrates clinical development, regulatory and commercialization services to help life‑science companies bring therapies to market faster. It provides end‑to‑end capabilities — clinical trials across phases and therapeutic areas, real‑world evidence and data analytics, medical affairs, market access, patient engagement and commercial launch services. With a global network of scientific, clinical and commercial experts, Syneos partners with biopharma, biotech and medtech clients to de‑risk development programs and accelerate product adoption.