Associate, Study Management II

This is a fully remote position, open to applicants in China.

📋 Description

• Execute various components of clinical studies while adhering to ICH/GCP standards, global regulations, and AbbVie policies and procedures.

• Assist the Study Project Manager in coordinating the cross-functional study team.

• Organize agendas and document minutes for Clinical Study Team meetings.

• Provide regular updates on study status to the cross-functional team and stakeholders, ensuring the CTMS is kept current.

• Aid in the creation of clinical study blueprints/protocols and related systems and documents, including informed consent forms, eCRFs, IRT, and CSR.

• Assist in the selection, scope development, management, and oversight of vendors in accordance with AbbVie processes and applicable regulations.

• Develop training materials related to studies for study teams, sites, and vendors.

• Proactively identify, address, and/or escalate issues related to the study.

• Engage in initiatives for process improvement.

⛳️ Requirements

• A Bachelor’s Degree or equivalent degree from outside the U.S. is required, typically in nursing or a scientific discipline.

• Registered Nurse licensure with an Associate’s Degree in Nursing and relevant experience is also acceptable.

• A minimum of two years of experience related to Pharma or clinical research, or a professional equivalent, is preferred.

• Strong analytical and critical thinking abilities.

• Effective communication skills.

🏝️ Benefits

• Equal opportunity employer.

• Dedicated to operating with integrity, fostering innovation, transforming lives, and serving the community.