Job Description

*Hybrid (3x per week onsite) preferred. Will consider remote candidates.

With supervision, oversees the direction, planning, execution and interpretation of clinical trials or research activities of a clinical development program.  Participates in cross-functional teams to generate, deliver and interpret high-quality clinical data supporting overall product scientific and business strategy.

Responsibilities

With appropriate supervision, manages the design and implementation of study protocols for a clinical development program in support of the overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie’s customers, markets, business operations and emerging issues.  Oversees project-related education of investigators, study site personnel and AbbVie study staff.  Responsibility may extend from early translational development activities to mature product lifecycle management strategies for internal and/or partnered programs.

Has responsibility for oversight of clinical studies, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule.  Along with Clinical Operations, is responsible for oversight of study enrollment and overall timelines for key deliverables.  Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols on which assigned.

Contributes to design, analysis, interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other program documents. 

May serve on a Clinical Strategy Team as the clinical representative for the protocols for which the incumbent has responsibility.  Contributes to the development of a rigorous, cross-functionally-aligned, vetted Clinical Development Plan in collaboration with matrix team members.

Participates in opinion leader interactions related to the disease area(s); partners with Medical Affairs, Commercial and other functions in these activities as required, consistent with corporate policies.

Stays abreast of professional information and technology through conferences, medical literature and other available training, to augment expertise in the therapeutic area.

Responsible for understanding the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements.  May be asked to contribute to regulatory responses and discussions.

Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research.