Remote Clinical Research Lead: Impact & Compliance

Valatam

Quilmes

Remote

ARS 92,241,000 - 138,361,000

Full time

5 days ago

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Benefits offered by this job

Health insurance

Retirement planning options

Global Employee Assistance Program (E"

Life assurance

Job summary

ICON, a global healthcare intelligence and clinical research organisation, is seeking a CRA II/Senior CRA to design and analyze clinical trials, interpret complex medical data, and contribute to the advancement of innovative therapies. The role involves site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance and patient safety throughout the trial process.

You will collaborate with investigators and site staff to facilitate smooth study conduct, perform

Qualifications

Bachelor's degree in a scientific or healthcare-related field.
Minimum of 1.5 years of experience as a Clinical Research Associate.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Strong organizational and communication skills, with attention to detail.
Ability to work independently and collaboratively in a fast-paced environment.

Responsibilities

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
Performing data review and resolution of queries to maintain high-quality clinical data.
Contributing to the preparation and review of study documentation, including protocols and clinical study reports