Director Study Management
Job Location:
Mississauga - Canada
Monthly Salary:
Posted:
Application Deadline:
Vacancies:
Job Summary
Job Title: Director Study Management
Location: Mississauga Ontario
At AstraZeneca we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial thinking big and working together to make the impossible a reality. If you are swift to action confident to lead willing to collaborate and curious about what science can do then youre our kind of person.
Recognizing the importance of individualized flexibility our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our head office is purposely designed with collaboration in mind providing space where teams can come together to strategize brainstorm and connect on key projects.
Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people the planet and our business are interconnected which is why were taking ambitious action to tackle some of the biggest challenges of our time from climate change to access to healthcare and disease prevention.
Introduction to Role:
TheDSMis responsible forleading developing supporting and providing direction toStudyManagement and Operations (SMO) personnel for project TA/scientific/technical and operationalrelated issues to enable delivery of drug projects andnon drugprojects. The DSM is ac countable for
resourcing SMO memberso nstudy teams to support delivery of clinical programs in R&D. The roleholder will alsobe responsible forembedding consistent ways of working across Hubs andbuildingSMO capabilities.
The DSM will ensure that direct reports are equipped with the right skills and capabilities tooptimally lead and deliver clinical trials. Take ownership and act as a change agent todriveconsistent implementation of globally agreed Clinical Operations and Clinical Development strategiesincluding processes and technology related to the delivery of studies.
Accountabilities:
- Line management of SMO staff
RecruitRetain& Develop SMO personnel.
Demonstrate AZ values.
Facilitate skills and capability training to SMO personnel to support their development.
Ensure personnel have been trained and work within compliance of ethics companypoliciesand standard procedures.
Role model and embed a performance driven culture and coach staff foroptimumperformance.
Develop and nurture capabilities of our present and future AZ leaders.
Manage performance including feed-forward and rewards.
Provideexpertiseand direction to support direct reports with proactive problem/risk
Delivery of projects
Maintain dialogue with Senior DSM and Snr Global Clinical Operations Program Director toanticipateproject requirements and mitigate risks to project delivery.
Allocate appropriately skilled SMO personnel to study delivery teams to ensure delivery of clinical studies to timebudgetand quality standardsin accordance withclinical performance targets.
Ensure staff understand global project priorities and specific project challenges: support staff/team to achieve project turning points and study results.
To work across departments to support the delivery of projects and organizational improvements.
Hub Leadership
Participate in setting and responsible for implementing the vision & strategy for theSMO Hub aligned with Clinical Operations and Hematologys Vision & Strategy.
Contribute to business strategy and streamline processes for drug/non-drug projects ordepartmental activities.
Lead and support change by encouraging diversity of solutions and implementingprocesschangesconsistently across SMO.
Act as a change Agent with local and global impact to ensure adoption of Global initiatives.
Promote and encourage innovation and creativity.
Work with Leadership team and Global Study Leads to achieveaccurateresource forecastingand develop solutions to efficiently and flexibly resource study teams.
Promote and encourage communication within and across Hubs and between BioPharma andOncology SMO.
Ensure quality and compliance to External Regulations and AZ Standards.
Work across the Hubs to develop global efficient ways-of-working.
Provide expert input into functional and cross-functional global processes.
Provide leadership in local Hub.
Foster the sharing of study delivery knowledge information and best practice on individualperformance to the study team members and their line managers to support their professionaldevelopment; may mentor less experienced colleagues.
Essential Skills/Experience:
Bachelors degree preferably in medical or biological science or related subject or equivalent qualification or experience.
10 or more years of experience in thepharmaceutical industry.
Comprehensive experience of clinical and Drug Development process within a pharmaceutical or clinical background.
Proven leadership and ability to promote motivation and empower othersin order toaccomplishindividual team and organizationalobjectives.
Thorough knowledge of Study Management processes in both local regulation and global environment.
An understanding of Oncology/Hematology TA.
Desireable Skills/Experience:
Advanced degree in a scientific subject area.
Line management experience.
Expert reputation within the business andIndustry.
Extensive knowledge of the latest technicalinformation.
Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with reduced budget and in less time.
Where can I find out more
- Our Social Media Follow AstraZeneca on LinkedIn AstraZeneca on Facebook AstraZeneca on Instagram US Footprint: Powering Scientific Innovation - YouTube
AstraZenecais an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment assessment and selection process and may be requested by emailing.
Annual base salary for this position ranges from 151884.00 to 199347.75.
AstraZeneca is committed to providing fair and equitable compensation opportunities to all colleagues. Our compensation policies and practices have been designed to allow colleagues to progress through the salary range over time as they progress in their role. The range provided in this posting represents an offer pay range used in a majority of situations. The base pay offered will vary depending on multiple individualized factors including the candidates skills and experience job-related knowledge and other specific business and organizational some cases offers outside the range may also be considered to address unique circumstances.
In addition our permanent positions offer an annual Variable Pay Bonus/Short Term Incentive opportunity as well as eligibility to participate in our equity-based long-term incentive program (if applicable to role). Benefits offered for permanent roles include a competitive Flex Benefits & Retirement Savings Program 4 weeks paid vacation and annual Personal Days. Fixed Term Contract/Temporary positions (excluding students) are offered a Contract Benefits Program.
We are using AI as part of the recruitment process.
This advertisement relates to a current vacancy.
Required Experience:
Director
About Company
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, ... View more
