Remote Oncology CRA: Drive Clinical Trials Impact

Translational Research in Oncology; Santa Fe Capital; Remote; ARS 108,178,000 - 154,540,000; Full time

Job summary

AbbVie seeks a qualified professional to advance clinical research by ensuring site engagement, effective monitoring, and high data integrity. You will collaborate with investigators, train site staff, and optimize recruitment while maintaining regulatory compliance and patient safety.

Responsibilities include mentoring CRAs, conducting site evaluations, and coordinating with central monitoring to mitigate risks.

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 a dynamic 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.

Responsibilities

• Primary point of contact for the investigative site and provide contextual information on the clinical trials.
• Aligns, trains and motivates the site staff and principal investigator on trial goals and patient treatment principles.
• Conducts site evaluation, training, routine and site-closure monitoring activities with compliance to protocol and ICH/GCP standards.
• Customize site engagement strategy and report progress using CRM tools.
• Connects study protocol and clinical concepts to trial execution and supports recruitment strategies.
• Mentor and train less experienced CRAs and participate in global/local task forces as needed.
• Ensure data quality and safety reporting and regulatory inspection readiness at sites.
• Manage investigator payments and site relationships as per contracts.

Skills

Cross-functional collaboration

Planning & organization

Interpersonal skills

Communication

Critical thinking

Problem solving

Education

Bachelor's Degree in health related disciplines

Tools

CRM tool

Job description

AbbVie seeks a qualified professional to advance clinical research by ensuring site engagement, effective monitoring, and high data integrity. You will collaborate with investigators, train site staff, and optimize recruitment while maintaining regulatory compliance and patient safety.

Responsibilities include mentoring CRAs, conducting site evaluations, and coordinating with central monitoring to mitigate risks.