AbbVie
10,000+ employees
Founded 2013
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.
Clinical Research Associate I
🔥 6 minutes ago
⚜️ Louisiana, Tennessee – Remote
💵 $75k - $142.5k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🦅 H1B Visa Sponsor
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AbbVie
10,000+ employees
Founded 2013
🏥 Healthcare
💼 Consulting
🏭 Manufacturing
Healthcare • Consulting • Manufacturing
AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.
📋 Description
• Advance AbbVie's pipeline by striving for excellence in clinical research • Partners with the investigator and site staff for meaningful and effective engagements • Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience • Considered as the primary point of contact for the investigative site, provides contextual information on the clinical trials • Connects stakeholder to the investigative sites and strengthens AbbVie’s positioning • Aligns, trains and motivates the site staff and principal investigator under supervision on the goals of the clinical trial program, protocol, and patient treatment principles for the trial ensuring a trusted partnership • Conducts site evaluation, site training, routine, and site closure monitoring activities under supervision, in compliance to the protocol and monitoring plans • Customize site engagement strategy for assigned study (ies) under supervision • Gather local/site insights and utilize site engagement tools such as the Customer Relationship Management (CRM) tool, to report/track progress and measure impact of that strategy • Evaluate and ensure effective recruitment and retention techniques/plans based on the patient disease journey • Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues • Ensures preventative and corrective action plans are put into place, as needed, to mitigate risk and promote compliance using a customer centric approach • Identifies, evaluates and recommends new/potential investigators/sites under supervision and support from more experienced CRAs • Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel • Ensures audit and regulatory inspection readiness at assigned clinical site at all times • Manages investigator payments as per executed contract obligations, as applicable
🎯 Requirements
• Bachelor’s degree or equivalent degree; health related preferred (e.g. Medical, Scientific, Nursing, Pharmacy) • Clinically related experience, preferably in clinical research coordinating or data management • Knowledge of appropriate therapeutic area indications is preferred • 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.
🏖️ Benefits
• paid time off (vacation, holidays, sick) • medical/dental/vision insurance • 401(k) • short-term incentive programs
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