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14 Apitoria Pharma Jobs
Data Solutions Coordinator
Apitoria Pharma
posted 13hr ago
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Job Description
The Role
As a Data Solutions Coordinator on the Regulatory Intelligence team at Redica Systems, you will play a critical role in monitoring and analyzing the global regulatory landscape within the life sciences industry. Your primary responsibility will be to support our regulatory intelligence products and services by actively participating in global monitoring, surveillance, and data acquisition activities. You will work closely with cross-functional teams to identify emerging trends in the pharmaceutical and MedTech regulatory environments and ensure the accuracy and integrity of our regulatory data.
This role is ideal for someone who is passionate about regulatory affairs, enjoys diving deep into data, and thrives in a collaborative, fast-paced environment. If you are driven by the opportunity to make a significant impact in a high-growth company and are eager to contribute to our mission of helping companies navigate complex regulatory landscapes, we want to hear from you!
As a Data Solutions Coordinator on the Regulatory Intelligence team at Redica Systems, you will play a critical role in monitoring and analyzing the global regulatory landscape within the life sciences industry. Your primary responsibility will be to support our regulatory intelligence products and services by actively participating in global monitoring, surveillance, and data acquisition activities. You will work closely with cross-functional teams to identify emerging trends in the pharmaceutical and MedTech regulatory environments and ensure the accuracy and integrity of our regulatory data.
This role is ideal for someone who is passionate about regulatory affairs, enjoys diving deep into data, and thrives in a collaborative, fast-paced environment. If you are driven by the opportunity to make a significant impact in a high-growth company and are eager to contribute to our mission of helping companies navigate complex regulatory landscapes, we want to hear from you!
Key Responsibilities
- Actively participate in global regulatory intelligence activities, including monitoring, acquiring, tracking, and categorizing information related to the evolving global regulatory landscape within the life sciences industry.
- Maintain a thorough awareness of all current and relevant regulations, guidelines, policies, procedures, and practices.
- Utilize a strong understanding of GXP to proactively identify, categorize, and analyze regulations, rules, and guidance document changes.
- Collaborate with teams to identify and assess emerging trends in the pharmaceutical and med tech regulatory environments.
- Conduct data quality checks to ensure the accuracy, completeness, and integrity of regulatory data.
- Monitor and report on key performance indicator (KPI) metrics related to regulatory activities.
- Ensure that all data acquisition and processing processes are clearly defined and consistently followed, while also recommending and implementing improvements where necessary.
About You
- Communicates Effectively: Develop and deliver clear, concise communications across multiple platforms, ensuring accurate and timely sharing of regulatory intelligence insights, updates, and trends with teams and stakeholders.
- Decision Quality: Analyze and evaluate regulatory data, rules, and guidance document changes to make informed, timely decisions that drive forward the organization s regulatory intelligence activities.
- Plans and Aligns : Organize and prioritize multiple time-sensitive projects related to monitoring, tracking, and categorizing global regulatory information, maintaining a high level of attention to detail to ensure data accuracy and relevance.
- Nimble Learning: Demonstrate a commitment to continuous learning by staying updated on the evolving global regulatory landscape, using new insights to improve regulatory intelligence processes and outcomes.
- Tech Savvy: Leverage digital tools and technology solutions to monitor regulatory changes, ensuring data accuracy and integrity while contributing to the company s digital transformation and innovation in regulatory intelligence.
- Engaged: You share our values and possess the essential competencies needed to thrive at Redica, as outlined here: https: / / redica.com / about-us / careers / .
- 2-4 years of experience in the pharmaceutical or medical device industries, with a focus on regulatory affairs or quality assurance.
- A Master s degree (M.S.) in Regulatory Affairs or Quality Assurance is preferred.
Employment Type: Full Time, Permanent
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