**MAIN PURPOSE OF THE ROLE** Individual contributor that works under limited supervision. Applies subject matter knowledge. Requires capacity to understand specific needs or requirements to apply skills/knowledge. **MAIN RESPONSIBILITIES** - Plans, directs, creates and communicates clinical study time-lines. - Gathers input from cross-functional teams and creates plans that help the team produce deliverables on schedule. - Ensures consistency of clinical study and processes across clinical trials. - Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations such as site and vendor selection, preparing clinical trial budgets.



- Ensures study is conducted within clinical trial protocols. - Monitors progress and follows up with team members and line managers when issues develop. **QUALIFICATIONS** Education Level Major/Field of Study or Equivalent Associates Degree (± 13 years) Experience/Background Minimum 1 year An Equal Chance Employer Abbot welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call (phone hidden) or email [email protected]

📌 Safety Specialist (Gurugram)
🏢 Abbott
📍 Gurugram