Senior Associate, Senior Data Manager, Clinical Data Sciences
- United States - Connecticut - Groton
- United States - New York - New York City
We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.
To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.
Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world.
Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes.
What You Will Achieve
You will play an important role in processing, reviewing and receiving clinical data and records from therapeutic groups as well as internal and outside investigators. You will ensure that accurate, timely, and consistent data reaches the clinical teams and other groups. You will be relied on for data management plans, including data preparation and validation activities, among others.
As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing important deliverables on time.
How You Will Achieve It
- Manage own time to meet agreed targets; develop plans for work activities on own projects within a team.
- Serve as Data Manager for one or more clinical trials assuming responsibility for Data Monitoring and Management (DMM) activities.
- Ensure operational excellence in collaboration with partners and colleagues for application of standards and develop data cleaning reports in support of the data review plan.
- Set-up and test data review listings to verify the quality and completeness of data as specified in Data Management Plan by reviewing data attributes populated by general users.
- Ensure lessons learnt during the study are documented and shared with other study teams to facilitate cross-study learning.
- Build good relationships with local and global SMEs from different fields, leverage their expertise in areas such as systems and process and proactively identify issues and work to create solutions.
Qualifications
Must-Have
- Bachelor's Degree.
- 3+ years’ experience.
- Demonstrated knowledge of data management processes and principles.
- Experience with web based data management systems.
- Working knowledge of electronic document management systems.
- Knowledge of International Conference on Harmonization and more specifically Good Clinical Practices.
- Thorough understanding of the processes associated with clinical study management and regulatory operations.
- Ability to manage tasks, time and priorities.
- Demonstrated effective verbal and written communication skills and adapt communications to audience.
Nice-to-Have
- Relevant pharmaceutical industry experience.
- Experience using data visualization tools.
- Proficient experience using commercial clinical data management systems and/or EDC products.
- Awareness of regulatory requirements and relevant data standards.
Other Job Details:
- Last Date to Apply: October 31, 2024
- Eligible for Relocation Package - NO
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