Clinical Research Associate I – Oncology

This is a fully remote position, open to applicants in United States.

📋 Description

• Propel AbbVie’s clinical research initiatives and aid in the creation of pioneering medicines.

• Act as the main liaison for investigative sites.

• Supply clinical trial details and facilitate connections between stakeholders and investigative sites.

• Align, train, and inspire site personnel and principal investigators regarding trial objectives, protocols, and patient treatment principles.

• Perform site evaluations, training, routine monitoring, and closure activities under supervision.

• Guarantee adherence to protocols, monitoring plans, regulations, GCPs, ICH Guidelines, AbbVie SOPs, and quality standards.

• Tailor site engagement strategies and monitor progress using CRM tools.

• Link study protocols, scientific principles, and clinical trial requirements to daily execution.

• Assess and support plans for patient recruitment and retention.

• Cultivate knowledge in therapeutic areas, assets, clinical landscapes, and patient journeys.

• Conduct ongoing risk assessments with the Central Monitoring team.

• Address site risk signals and implement preventive and corrective action plans.

• Identify, assess, and recommend investigators and clinical sites under supervision.

• Ensure data integrity and timely submissions, including safety event reporting and follow-up.

• Maintain readiness for audits and regulatory inspections.

• Oversee investigator payments in accordance with executed contracts, as applicable.

⛳️ Requirements

• Relevant tertiary qualification in health-related fields (Medical, Scientific, Nursing) preferred, or equivalent experience.

• Experience related to clinical fields, ideally in clinical research coordination or data management.

• Familiarity with relevant therapeutic area indications is preferred.

• Capability to comprehend and apply scientific concepts to the execution of clinical trials.

• Awareness of local regulatory and legal standards, ICH/GCP Guidelines, and applicable policies.

• Ability to collaborate and work across functions effectively.

• Strong planning and organizational skills; adept at functioning in a dynamic environment with multiple projects and deadlines.

• Proficient in leveraging technology, tools, and resources.

• Strong critical thinking and sound judgment to tackle clinical site challenges.

• Excellent written, verbal, active listening, and presentation abilities.

• Capacity to establish and nurture site relationships and trusted partnerships.

• Uphold integrity in alignment with AbbVie’s code of business conduct and leadership principles.

• Self-driven and focused on achieving timely, high-quality outcomes in a fast-paced environment.

🏝️ Benefits

• Paid time off (vacation, holidays, sick leave).

• Medical, dental, and vision insurance.

• 401(k) plan.

• Eligibility for short-term incentive programs.

• Equal opportunity employment.

• Reasonable accommodations for applicants with disabilities.