Clinical Operations Manager

Responsibilities

• Provides leadership and oversight to the clinical research team
• Performs accompanied visits (on-site and off-site) accelerates AbbVie priority programs through close collaboration with internal and external stakeholders
• Conducts trend analysis and gap assessments to proactively identify training and developmental opportunities for assigned personnel
• Addresses gaps effectively to help assigned personnel achieve country and site level KPIs and metrics.
• Ensures adherence to applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie
• Standard Operating Procedures (SOPs), and to quality standards in conducting clinical research. Stay abreast of new and/or evolving local regulations, guidelines and policies.
• Supports, trains, and oversees assigned personnel to ensure that they maintain audit and inspection readiness at assigned sites/studies. Prepare and follow up on site and country audits, CAPA preparation and implementation.
• Utilizes reports from available systems and country/area model to accomplish *In alignment with AbbVie research goals, priorities, an
• specific study timelines
• Ensure resource utilization to address business priorities and maximize team impact to delivery of the pipeline
• Accountable for the budget management and payments of the assigned studies conducted by their assigned team, as applicable. Creates an inclusive environment to enable team members to reach their full potential.
• Helps team connect strategy to execution and promotes collaboration with stakeholders to effectively deliver pipeline.
• Leads and supports the team to understand the business strategy and vision. Drives and implements change through effective communication and management.
• May participate and/or lead global/local task forces and initiatives. Responsible for activities as assigned by Line Manager. Proactively identifies opportunities at local/ global levels and proposes solutions to create
• efficiencies and streamline/improve processes. Partners with research sites with high levels of coordinated and impactful site engagement with KOLs, National Leads, Principal Investigators and site staff positioning AbbVie as the partner of choice in clinical trials.

Requirements

• Education: Bachelors or equivalent degree, health related (e.g. Medical, Scientific, Nursing, Pharmacy) preferred.
• Monitoring Experience: Minimum 3 years.
• Exhibits strong planning and organizational skills. Experience across multiple therapeutic areas and study phases.
• Mentoring and coaching skills. Has the ability to provide transparent and timely feedback to raise the bar on individual and team performance.
• Drives innovation and continuous process improvement.
• Acts with integrity in accordance with AbbVie code of business conduct and leadership values.
• Deals comfortably with risk and ambiguity, changing course when needed.
• Ability to make timely, high-quality decisions based on available data and information.
• Ability to work independently and take initiative/ownership. Ability to adapt and move quickly.
• Applicable only to applicants applying to a posi

Benefits

Additional Information

Purpose : To advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients, and leveraging new capabilities to drive industry leading performance. This role is accountable for building and leading high performing clinical research teams who partner with investigative sites for meaningful and effective engagements, striving to position AbbVie as the partner of choice in clinical trials. Accountable for teams' clinical trial performance, providing strategic planning, oversight and direction of the team to ensure on time, within budget and quality delivery of clinical studies. Establish partnership with internal stakeholders to drive insightful and impactful interactions and promote the value of the clinical research team through the contribution to the R&D portfolio success.

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