Advance AbbVie pipeline by striving for excellence in clinical research
Partners with investigator and site staff for meaningful engagements positioning AbbVie as the choice in clinical trials
Focus on site clinical research ensuring appropriate conduct of the trial while driving improvement in data integrity and compliance
Considered as the primary point of contact for the investigative site
Provides contextual information on clinical trials and connects stakeholders to investigative sites
Aligns, trains and motivates site staff and principal investigator under supervision
Conducts site evaluation, site training, routine, and site closure monitoring activities under supervision
Customize site engagement strategy for assigned studies under supervision
Gather local/site insights and utilize site engagement tools such as CRM tool
Evaluate and ensure effective recruitment and retention techniques/plans based on patient disease journey
Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team
Ability to think critically to resolve site risk signals
Ensures quality of data submitted from study sites and assures timely submission of data
Manages investigator payments as per executed contract obligations

Bachelor’s degree required; health related preferred (e.g. Medical, Scientific, Nursing, Pharmacy)
Clinically related experience, preferably in clinical research monitoring, coordinating or data management
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
Knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies
Able to work collaboratively and cross functionally to develop and sustain working relationships
Demonstrate planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines
Ability to leverage technology, tools and resources to provide customer centric support based on the health of the site
Ability to use functional expertise with appropriate guidance, leverage critical thinking skills and apply good judgement to address clinical site issues
Interpersonal skills with strong written, verbal, active listening and presentation skills, with ability to establish and leverage site relationships and trusted partnerships through engagement, motivation, and training
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

Clinical Research Associate I

Key skills