Clinical Research Associate I
A
AbbViePharmaceutical Research
United StatesFull-TimeEntry
SalaryUSD 75000 - 142500 / year
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Job Details
- Required Skills
- CRMData management
Requirements
- Appropriate tertiary qualification in health-related disciplines (Medical, Scientific, Nursing) preferred.
- Clinically related experience, preferably in clinical research coordinating or data management.
- Knowledge of existing and emerging local regulatory and legal requirements.
- In-depth understanding of ICH/GCP guidelines and applicable policies.
- Ability to understand and apply scientific concepts related to clinical trial conduct.
- Demonstrated planning and organizational skills for managing competing projects and deadlines.
- Proficiency in leveraging technology, tools, and CRM systems for site support.
- Strong interpersonal skills with effective written, verbal, and active listening abilities.
- Ability to work collaboratively and cross-functionally.
- Commitment to integrity and AbbVie's code of business conduct.
Responsibilities
- Serve as the primary point of contact for the investigative site, providing contextual information on clinical trials and strengthening site partnerships.
- Train and motivate site staff and investigators on study goals, protocols, and patient treatment principles.
- Conduct site evaluation, routine, and closure monitoring activities in compliance with ICH/GCP guidelines and AbbVie SOPs.
- Execute site engagement strategies using CRM tools to report progress and measure impact.
- Perform proactive risk assessment to detect performance or safety issues and implement corrective action plans.
- Ensure audit and regulatory inspection readiness and manage investigator payments per contract obligations.
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