Senior Clinical Research Associate — Remote, Global Trials

Worldwide Clinical Trials; Tandil; Remote; ARS 900,000 - 1,300,000; Full time

Job summary

Worldwide Clinical Trials seeks a Clinical Research Associate to oversee site qualification, initiation, monitoring, and close-out visits within Argentina. You will ensure patient safety, data quality, and regulatory compliance while coordinating with investigative sites and sponsor teams.

The role requires MD/Pharmacy or equivalent degree with CRA experience, strong knowledge of GCP/ICH or FDA/EU regulations, and proficiency with EDC systems, MS Office, and IxRS.

Qualifications

• Education and experience: MD or Pharmacy degree (MSPH, PharmD, PhD, or equivalent) with at least one year of CRA Level I experience; OR a four-year degree in medical/biological/health/science with two years of CRA experience; OR two-year college with two years of CRA experience.
• Strong knowledge of clinical research principles, GCP, ICH, FDA/EU regulations, and SOPs.
• Experience across 3–5 therapeutic areas or depth in 2–3 areas.
• Proficiency with MS Office, IxRS, and EDC systems.

Responsibilities

• Conduct site qualification, initiation, interim monitoring, and close-out visits per protocol and GCP.
• Monitor study conduct, source data, informed consent, and safety information.
• Assess and train site staff on protocol requirements and issues.
• Ensure regulatory and site documentation is complete and maintained.
• Coordinate data queries and safety-event reporting with sites.
• Oversee investigational product receipt, accountability, and destruction.
• Maintain clear, timely visit reports and communicate with sites.
• Contribute to protocols, CRFs, monitoring plans, and feasibility studies.
• Assist in training other CRAs on accompanied site visits.

Skills

Clinical research knowledge

GCP & regulations

EDC systems

English + local language

Travel readiness

Education

MD/Pharmacy degree

Four-year life sciences degree

Nursing degree

Tools

IxRS

Microsoft Office

Job description

Worldwide Clinical Trials seeks a Clinical Research Associate to oversee site qualification, initiation, monitoring, and close-out visits within Argentina. You will ensure patient safety, data quality, and regulatory compliance while coordinating with investigative sites and sponsor teams.

The role requires MD/Pharmacy or equivalent degree with CRA experience, strong knowledge of GCP/ICH or FDA/EU regulations, and proficiency with EDC systems, MS Office, and IxRS.