The Specialist drives and executes start up and maintenance activities for assigned studies/sites
Responsible for site activation plans, risk assessment, regulatory submissions, IP release, and
Collaborates with Regulatory, CTS, Contract Manager, CRA, and other stakeholders to ensure

🎯 Requirements

Bachelor's Degree (health care/scientific field) preferred or equivalent experience.
1-2 years clinical research, with 1+ years in study start up management for designated region.
Experience with remote/virtual teams; strong analytical and communication skills (English and
Knowledge of ICH and GCP; understanding of local regulatory environment.
Demonstrated ability to manage multiple priorities in fast-paced settings.

🎁 Benefits

AbbVie equality commitments; information on accommodations available on company site.

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