Manager, Clinical Data Scientist, Clinical Data Sciences
PfizerAbout the role
Use Your Power for Purpose
At Pfizer, our mission is to empower healthcare decisions regarding the safe and appropriate use of medicines for patients. You will play a pivotal role in improving patients' lives by ensuring the accuracy, timeliness, and consistency of clinical data. Your work will bridge evidence-based medical decision support with colleagues and stakeholders, enhancing health and treatment outcomes. By developing robust frameworks, providing unbiased expertise, and addressing data gaps, you will contribute to better health outcomes and the safe use of medicines. Your dedication will help Pfizer achieve new milestones and support patients worldwide.
What You Will Achieve
In this role, you will:
- Lead and manage people, technology, and financial resources within the department.
- Actively share knowledge and identify potential improvements in processes or products, taking risks to develop innovative ideas.
- Solve moderately complex problems within your expertise and assist with issues outside the department.
- Oversee operational activities to support the department's short-term goals and manage the performance of direct reports through goal setting, coaching, and ongoing assessment.
- Recognize the need for development in others, collaborate to create development plans, and solicit input to explain complex concepts and persuade others.
- Process, review, and receive patient data and records, ensuring accurate, timely, and consistent clinical data reaches the medical department and other groups.
- Develop data management plans, including data preparation and validation activities, and guide operational teams in managing projects and identifying areas for improvement.
- Facilitate agreements between different teams, taking a leadership role, and serve as a Clinical Data Scientist and Trial Lead for clinical trials.
- Act as a technical resource to study teams for data visualization and reporting tools, ensuring operational excellence in collaboration with partners.
- Perform central monitoring activities, plan and execute communication strategies, and engage customer populations effectively.
Here Is What You Need (Minimum Requirements)
- BA/BS with at least 4 years of experience or MBA/MS with at least 2 years of experience or PhD/JD with any years of experience or associate's degree with at least 8 years of experience or high school diploma (or equivalent) with at least 10 years of relevant experience
- Comprehensive understanding of all phases of clinical trials
- Familiarity with clinical research, FDA regulations, and International Conference on Harmonization Good Clinical Practices (GCDMP)
- Strong project and risk management skills
- Excellent verbal and written communication abilities
- Capability to handle multiple tasks and projects efficiently
- Proficiency in the Windows environment and its applications
Bonus Points If You Have (Preferred Requirements):
- Master's degree
- Contract Research Organization (CRO) and vendor oversight experience
- Proficient in using commercial clinical data management systems and/or EDC products
- Ability to adapt to changing priorities and manage multiple projects simultaneously
- Strong interpersonal skills and the ability to build relationships with stakeholders
Other Job Details:
- Last Date to Apply for Job: 28 JANUARY 2025
- Eligible for Employee Referral Bonus
- Not Eligible for Relocation Assistance
Work Location Assignment: Hybrid
Relocation assistance may be available based on business needs and/or eligibility.
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