Senior Clinical Site Leader

AstraZeneca plc

United States

Hybrid

USD 138,000 - 207,000

Full time

14 days+

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Job summary

AstraZeneca plc seeks an Associate Director Clinical Research to lead a dedicated team and ensure successful delivery of interventional studies in line with ICH-GCP and AZ procedures. You will oversee site management from identification to closeout, manage staffing, and drive development plans for CRAs/CSAs to achieve study goals with quality and speed.

You will mentor staff, secure necessary resources, maintain inspection readiness, and partner with senior directors to deliver country-level

Qualifications

  • Bachelor’s degree in related discipline, preferably life science.
  • Experience in pharmaceutical industry, Clinical Operations (CRA / SrCRA / LSAD) or related fields.
  • Knowledge of drug development, ICH-GCP, country regulations, and AZ Therapeutic Areas.
  • Clinical Study Management including monitoring, study drug handling and data management.

Responsibilities

  • Provide leadership to a dedicated team and foster a high performing team climate.
  • Ensure adequate resourcing for all assigned clinical studies.
  • Monitor workload and ensure fair distribution among staff.
  • Oversee development and performance management of direct reports.
  • Maintain eTMF completeness and inspection readiness.
  • Review monitoring reports and QC visits per SOPs.
  • Support country-level SMM study delivery targets.

Skills

Personal Effectiveness
Learning Agility
Financial Competency
Tech & Process
English Proficiency
Integrity & Ethics
Team Leadership
Quality Delivery
Travel Readiness
Drivers License
Communication
Risk-Based Thinking
Talent Planning
Coaching
Collaboration

Education

Bachelor’s degree in related discipline

Job description

AstraZeneca plc seeks an Associate Director Clinical Research to lead a dedicated team and ensure successful delivery of interventional studies in line with ICH-GCP and AZ procedures. You will oversee site management from identification to closeout, manage staffing, and drive development plans for CRAs/CSAs to achieve study goals with quality and speed.

You will mentor staff, secure necessary resources, maintain inspection readiness, and partner with senior directors to deliver country-level

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