Remote Oncology CRA: Drive Site Excellence

Translational Research in Oncology; Santa Fe Capital; Remote; ARS 115,905,000 - 169,994,000; Full time

Benefits offered by this job

Health insurance

401(k) plan

Paid time off

Job summary

AbbVie is seeking a Clinical Site Monitor/CRA to advance our clinical research programs worldwide. You will be the primary contact at investigative sites, ensure protocol compliance, recruit and retain participants, and maintain data integrity while coordinating with global teams.

You will mentor junior CRAs, participate in task forces, and help ensure safety and regulatory readiness across sites. The role requires strong collaboration, organization, and ability to manage multiple trials in a

Qualifications

• Bachelor's Degree in health related disciplines (Medical, Scientific, Nursing) preferred.
• Minimum of 1 year of clinically related experience, of which a period of 6 months is required in clinical research monitoring of investigational drug or device trials.
• Knowledge of appropriate therapeutic area indications is preferred with the ability to understand and apply scientific concepts as they relate to the conduct of clinical trials.
• Advanced knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies.
• Demonstrate strong cross-functional collaboration skills among internal and external stakeholders.
• Demonstrate strong planning and organizational skills and the ability to work effectively and efficiently in adynamic environment with competing projects and deadlines.
• Advanced ability to leverage technology, tools and resources to provide customer centric support based on the health of the site.
• Strong interpersonal skills with excellent written, verbal, active listening and presentation skills, with ability to establish and leverage site relationships and trusted partnerships through engagement, motivation, and training.
• Ability to use functional expertise with appropriate guidance, leverage critical thinking skills and apply good judgement to address clinical site issues.
• Acts with integrity in accordance with AbbVie code of business conduct and leadership values. Self-motivated individual focused on delivering timely and quality outcomes in a fast-paced environment.

Responsibilities

• Serve as primary contact for investigative sites and strengthen AbbVie’s positioning.
• Aligns and motivates site staff and investigators on trial goals.
• Conducts site evaluation, training, and monitoring per SOPs and GCP.
• Develops site engagement strategies and uses CRM to measure impact.
• Supports patient recruitment and protocol compliance.
• Mentor CRAs and participate in global/local task forces.
• Monitor sites for risk and ensure corrective actions.
• Identify potential investigators/sites for trials.
• Ensure data quality and timely reporting of safety events.
• Maintain audit readiness at clinical sites.

Skills

Cross-functional collaboration

Planning & organizational skills

Strong interpersonal skills

Critical thinking

Mentoring Others

Education

Bachelor's Degree in health related disciplines

Tools

CRM tool

Job description

AbbVie is seeking a Clinical Site Monitor/CRA to advance our clinical research programs worldwide. You will be the primary contact at investigative sites, ensure protocol compliance, recruit and retain participants, and maintain data integrity while coordinating with global teams.

You will mentor junior CRAs, participate in task forces, and help ensure safety and regulatory readiness across sites. The role requires strong collaboration, organization, and ability to manage multiple trials in a