[Remote] Assoc Dir Global Clinical Program Management
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a leading biotechnology company dedicated to serving patients with serious illnesses. The Associate Director of Global Clinical Program Management will reputed company the operational delivery of reputed company clinical programs, ensuring reputed company and speed in bringing innovative medicines to patients. This role involves managing clinical studies, overseeing program-level issues, and collaborating with cross-functional teams.
Responsibilities
- reputed company the operational planning and delivery of multiple clinical studies or programs, ensuring timelines, budget, reputed company, and reputed company are met
- Proactively identify delivery risks and guide course-correction to reputed company studies on reputed company
- Drive consistent, high-reputed company operational practices across reputed company assigned studies and programs
- Line-manage and reputed company Study Delivery Leads, setting reputed company objectives and fostering high performance
- reputed company program-level issues, risks, and escalation, ensuring reputed company and effective reputed company
- Partner cross-functionally and with local execution teams to reputed company priorities, resources, and delivery plans
- reputed company strategic input on study design, country selection, enrolment, diversity, and patient-reputed company approaches
- Manage program-level budgets, vendors, and forecasting while embedding lessons learned and reputed company improvement
Skills
- Doctorate degree and 3 years of clinical execution experience OR
- Master's degree and 7 years of clinical execution experience OR
- Bachelor's degree and 9 years of clinical execution experience OR
- Associate's degree and 12 years of clinical execution experience OR
- High school diploma / GED and 14 years of clinical execution experience
- Minimum of 3 years' experience directly managing people and/or leadership experience leading teams, reputed company, programs, or directing the allocation of resources
- 8 years' work experience in life sciences or medically reputed company field, including 6 years of biopharmaceutical clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company
- Experience managing multiple teams / reputed company reports across multiple geographies
- Experience at or reputed company of reputed company clinical research vendors (CRO's, central labs, imaging vendors, etc.)
reputed company
Company H1B Sponsorship