
Local Study Associate Director (12-month contract)
Are you a passionate and driven individual with a strong background in local clinical research? Do you thrive in a dynamic and fast-paced environment? AstraZeneca is seeking a highly motivated and experienced Local Study Associate Director to join our team for a 12-month contract. As the Local Study Associate Director, you will play a vital role in the development and execution of clinical studies, ensuring compliance with regulations and guidelines. If you have a proven track record of success in clinical research and possess excellent leadership and communication skills, we encourage you to apply for this exciting opportunity. Join us in our mission to improve patient outcomes and make a positive impact on global healthcare.
- Lead and oversee the development and execution of local clinical studies within AstraZeneca, ensuring compliance with all relevant regulations and guidelines.
- Collaborate with cross-functional teams and external partners to ensure timely and high-quality delivery of clinical studies.
- Develop and maintain study timelines, budgets, and resources to ensure successful study completion.
- Conduct risk assessments and develop mitigation plans to address any potential issues or challenges during the study.
- Manage and oversee study sites, including monitoring site performance, providing guidance on study protocols, and ensuring data integrity and accuracy.
- Serve as a subject matter expert on local clinical research regulations and guidelines, providing guidance and support to team members and stakeholders.
- Communicate study progress, issues, and results to internal and external stakeholders, including senior leadership, investigators, and regulatory authorities.
- Identify and implement process improvements to enhance the efficiency and effectiveness of clinical studies.
- Mentor and train junior team members to ensure their professional development and growth.
- Actively contribute to the development of study protocols, informed consent forms, and other study-related documents.
- Ensure all study activities are conducted in accordance with ethical and safety standards.
- Foster a positive and collaborative team environment to support the company's mission and values.
- Stay updated on industry trends, regulations, and best practices to continuously improve study processes and outcomes.
- Maintain accurate and up-to-date study documentation and records.
- Represent AstraZeneca at external meetings and conferences related to local clinical research as needed.
Minimum Of 5 Years Of Experience In Clinical Research Or Related Field, With At Least 2 Years In A Leadership Or Management Role.
Bachelor's Degree In Life Sciences Or Related Field, With Preference For Advanced Degree Such As Master's Or Phd.
In-Depth Knowledge Of Local Regulations And Guidelines For Conducting Clinical Trials, Including Ich-Gcp And Local Ethics Committee Requirements.
Strong Project Management Skills, With Demonstrated Ability To Lead Cross-Functional Teams And Manage Multiple Projects Simultaneously.
Excellent Communication And Interpersonal Skills, With Ability To Build And Maintain Relationships With Internal And External Stakeholders.
Research
Strategic Planning
Communication Skills
Project Management
Data Analysis
Market Research
Time Management
Problem Solving
Budget management
Report Writing
Team Leadership
Stakeholder engagement
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Teamwork
Active Listening
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Local Study Associate Director (12-month contract) in Mississauga, ON, Canada is $90,000-$120,000 CAD per year. This salary range may vary depending on the specific job responsibilities, experience level, and company size.
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AstraZeneca plc is a British-Swedish multinational pharmaceutical and biopharmaceutical company.

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